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v3.26.3
Disaggregated Revenues (Tables)
9 Months Ended
Sep. 30, 2026
Disaggregation of Revenue [Abstract]  
Schedule of Disaggregation of Revenue by Nature
The following table provides information regarding total revenues (dollars in thousands):
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)(unaudited)
Net product sales
Qelbree$90,824 $81,416 $257,906 $223,708 
GOCOVRI42,650 40,849 115,420 108,198 
ONAPGO17,075 6,806 38,996 8,410 
Trokendi XR10,213 10,043 28,103 34,037 
Oxtellar XR7,957 12,016 24,161 33,851 
APOKYN6,490 10,387 20,541 38,183 
Other(a)
3,367 7,025 9,915 22,138 
Total net product sales178,576 168,542 495,042 468,525 
Collaboration revenue (ZURZUVAE)(b)
41,697 20,164 104,690 20,164 
Royalty, licensing, and other revenues6,498 3,397 53,802 18,691 
Total revenues$226,771 $192,103 $653,534 $507,380 
___________________________________________
(a) Includes net product sales of MYOBLOC, XADAGO and Osmolex ER.
(b) Includes the Company's proportionate share of net sales of ZURZUVAE.
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v3.26.3
Summary of Significant Accounting Policies (Policies)
9 Months Ended
Sep. 30, 2026
Accounting Policies [Abstract]  
Basis of Presentation
Basis of Presentation
The Company's unaudited condensed consolidated financial statements have been prepared in accordance with the requirements of the U.S. Securities and Exchange Commission (SEC) for interim financial information. As permitted under Generally Accepted Accounting Principles in the United States (U.S. GAAP), certain notes and other information have been omitted from the interim unaudited condensed consolidated financial statements presented in this Quarterly Report on Form 10-Q. Therefore, these unaudited condensed consolidated financial statements should be read in conjunction with the Company's most recent Annual Report on Form 10-K, for the year ended December 31, 2025, filed with the SEC.
In management's opinion, the unaudited condensed consolidated financial statements include all normal and recurring adjustments necessary for a fair presentation of the Company's financial position, results of operations, and cash flows. The results of operations for any interim period are not necessarily indicative of the Company's future quarterly or annual results.
The Company, which is primarily located in the U.S., operates in one operating segment.
Reclassifications
Reclassifications
The prior year amounts related to the caption Noncash lease expense have been reclassified from the caption Other noncash adjustments, net in the condensed consolidated statements of cash flows to conform to current year presentation. The reclassifications did not affect the other condensed consolidated financial statements.
Consolidation
Consolidation
The Company's unaudited condensed consolidated financial statements include the accounts of Supernus Pharmaceuticals, Inc. and its wholly owned subsidiaries. These are collectively referred to herein as "Supernus" or "the Company." Supernus Pharmaceuticals, Inc. and each of its subsidiaries are distinct legal entities. All material intercompany transactions and balances have been eliminated in consolidation.
The unaudited condensed consolidated financial statements reflect the consolidation of entities in which the Company has a controlling financial interest. In determining whether there is a controlling financial interest, the Company considers if it has a majority of the voting interests of the entity, or if the entity is a variable interest entity (VIE) and if the Company is the primary beneficiary. In determining the primary beneficiary of a VIE, the Company evaluates whether it has both: the power to direct the activities of the VIE that most significantly impact the VIE's economic performance; and the obligation to absorb losses of, or the right to receive benefits from the VIE that could potentially be significant to that VIE. The Company's judgment with respect to its level of influence or control of an entity involves the consideration of various factors, including the form of an ownership interest; representation in the entity's governance; the size of the investment; estimates of future cash flows; the ability to participate in policymaking decisions; and the rights of the other investors to participate in the decision making process, including the right to liquidate the entity, if applicable.
If the Company is not the primary beneficiary of the VIE, and an ownership interest is maintained in the entity, the interest is accounted for under the equity or cost methods of accounting, as appropriate.
The Company continuously assesses whether it is the primary beneficiary of a VIE as changes to existing relationships or future transactions may affect its conclusions.
Use of Estimates
Use of Estimates
The Company bases its estimates on: historical experience; forecasts; information received from its service providers; information from other sources, including public and proprietary sources; and other assumptions that the Company believes are reasonable under the circumstances. Actual results could differ materially from the Company's estimates. The Company periodically evaluates the methodologies employed in making its estimates.
Revenue Recognition
Revenue Recognition
The Company determines revenue recognition for its contractual arrangements with customers based on the following five steps in accordance with Accounting Standards Codification (ASC) Topic 606, Revenue from Contracts with Customers (ASC 606): (1) identify each contract with a customer; (2) identify the performance obligations in the contract; (3) determine the transaction price; (4) allocate the transaction price to the performance obligations in the contract; and (5) recognize revenue when (or as) the Company satisfies the relevant performance obligation. The Company only applies the five-step model to contracts when it is probable that the Company will collect the consideration it is entitled to in exchange for the goods or services it transfers to the customer. The Company recognizes revenue in an amount that reflects the consideration the Company expects to receive in exchange for those goods or services. The Company does not adjust revenue for any financing effects in transactions where the Company expects the period between the transfer of the goods or services and collection to be less than one year.
Collaborative Arrangements
Collaborative Arrangements
The Company has a collaboration agreement with Biogen Inc. (Biogen) (Biogen Collaboration Agreement) for the co-commercialization of ZURZUVAE in the U.S. ZURZUVAE is approved for the treatment of PPD in the U.S. ZURZUVAE is not approved for the treatment of Major Depressive Disorder (MDD) in the U.S.
The Company also has a collaboration agreement with Shionogi & Co., Ltd. (Shionogi) (Shionogi Collaboration Agreement) whereby the Company is entitled to receive royalties and milestone payments upon achievement of certain milestones related to the sale of zuranolone for the treatment of MDD in Japan, Taiwan and South Korea (the Shionogi Territory).
At contract inception, the Company analyzes its collaboration arrangements to assess whether they are within the scope of Accounting Standards Codification Topic 808, Collaborative Arrangements (ASC 808) to determine whether such
arrangements involve joint operating activities performed by parties that are both active participants in the activities and exposed to significant risks and rewards dependent on the commercial success of such activities. This assessment is performed throughout the life of the arrangement based on changes in the responsibilities of all parties in the arrangement. For collaboration arrangements within the scope of ASC 808 that contain multiple elements, the Company first determines which elements of the collaboration are deemed to be within the scope of ASC 808 and those that are more reflective of a vendor-customer relationship and therefore within the scope of Accounting Standards Codification Topic 606, Revenue from Contract with Customers, (ASC 606). For elements of collaboration arrangements that are accounted for pursuant to ASC 808, an appropriate recognition method is determined and applied consistently, either by analogy to authoritative accounting literature or by applying a reasonable and rational policy election.
For those elements of the arrangement that are accounted for pursuant to ASC 606, the Company performs the five-step model under ASC 606 as noted above to determine the appropriate amount of revenue to be recognized as it fulfills its obligations under each of its agreements and presents the arrangement as Royalty, licensing and other revenue or Collaboration revenue (ZURZUVAE) in the condensed consolidated statements of earnings (loss).
For those elements of the arrangement that are accounted for pursuant to ASC 808, the Company evaluates the income statement classification for presentation of amounts due from or owed to other participants associated with multiple activities in a collaboration arrangement based on the nature of each separate activity. Payments or reimbursements that are the result of a collaborative relationship instead of a vendor-customer relationship are recorded as an increase to Collaboration revenue (ZURZUVAE), an increase to or reduction of Cost of revenues, Research and development expense, or Selling, general and administrative expense, depending on the nature of the activity.
The Company applies ASC 808 and ASC 606 to the following collaboration agreements:
•Biogen - The Company has a collaboration agreement with Biogen for the co-commercialization of ZURZUVAE in the U.S. Revenues from the Biogen Collaboration Agreement include the Company’s share of ZURZUVAE revenues as that element of the agreement is accounted for under ASC Topic 808. The Company reports as Collaboration revenue (ZURZUVAE) its share of ZURZUVAE revenues, which is 50% of total net revenue recorded by Biogen for ZURZUVAE in the U.S.
The Company also identified the following promises in the Biogen Collaboration Agreement that were evaluated under the scope of ASC 606: delivery of (i) a co-exclusive license for SAGE-217 products in the U.S.; (ii) an exclusive license for SAGE-217 products outside of the United States other than Japan, the Republic of Korea, and Taiwan (Biogen Territory); (iii) commercial manufacturing supply of active pharmaceutical ingredient (API) and bulk drug product for SAGE-217 products in the Biogen Territory, and (iv) commercial manufacturing supply of API and bulk drug product for SAGE-217 in the U.S.
The Company also evaluated whether certain options outlined within the Biogen Collaboration Agreement represented material rights that would give rise to a performance obligation and concluded that none of the options convey a material right to Biogen and therefore are not considered separate performance obligations within the Biogen Collaboration Agreement.
The Company assessed the above promises at contract inception and determined that the co-exclusive license for SAGE-217 products in the U.S. is reflective of a vendor-customer relationship and therefore represent performance obligations within the scope of ASC 606. The co-exclusive license for SAGE-217 products in the U.S. is considered functional intellectual property and distinct from other promises under the contract. The exclusive license for SAGE-217 products in the Biogen Territory is considered a functional license that is distinct in the context of the Biogen Collaboration Agreement as Biogen can benefit from the license on its own or together with other readily available resources. As the co-exclusive license in the U.S. and the exclusive license in the Biogen Territory are delivered at the same time, they are considered one performance obligation at contract inception. The commercial manufacturing supply of API and bulk drug product for SAGE-217 products for the Biogen Territory, as well as in the U.S., are considered distinct in the context of the Biogen Collaboration Agreement as Biogen can benefit from the manufacturing services together with the licenses transferred by the Company at the inception of the Biogen Collaboration Agreement. Therefore, each represents a separate performance obligation within a contract with a customer under the scope of ASC 606 at contract inception. Accordingly, the transactions are recorded in Royalty, licensing, and other revenues.
•Shionogi - The Company also has a collaboration agreement with Shionogi whereby the Company is entitled to receive royalties and milestone payments upon achievement of certain milestones. The Shionogi Collaboration Agreement also includes arrangement for the supply of drug product for Shionogi’s clinical trials. The Company concluded that Shionogi meets the definition of a customer because the Company is delivering intellectual property and know-how rights for the
zuranolone program in support of territories in which the parties are not jointly sharing the risks and rewards. In addition, the Company determined that the Shionogi Collaboration Agreement met the requirements to be accounted for as a contract, including that it is probable that the Company will collect the consideration to which the Company is entitled in exchange for the goods or services that will be delivered to Shionogi. The Company assessed the promises at contract inception and determined that the license to zuranolone and supply of products to Shionogi are reflective of a vendor-customer relationship and therefore represent performance obligations within the scope of ASC 606.
The Company determined that the performance obligations in the Shionogi Collaboration Agreement included the license to zuranolone and the supply of certain materials during the clinical development phase, which includes the supply of API. The performance obligation related to the license to zuranolone was determined to be distinct from other performance obligations and therefore was a separate performance obligation for which control was transferred upon signing, and is recorded in Royalty, licensing, and other revenues. The obligation to provide certain clinical materials, including API for use during the development period, was determined to be a separate performance obligation, and is recorded in Royalty, licensing, and other revenues.
For additional information on the collaboration agreements with Biogen and Shionogi, as well as the Company's other collaboration arrangements, refer to Note 15, Collaboration Agreements.
Advertising Expense
Advertising Expense
Advertising expense includes the cost of promotional materials and activities, such as printed materials and digital marketing, marketing programs and speaker programs. The cost of the Company's advertising efforts is expensed as incurred.
In addition, under the collaboration agreement with Biogen, the Company and Biogen equally share in the costs of development and commercialization of ZURZUVAE. Commercial activities under the collaboration agreement may include advertising expenses. The Company's proportionate share of the costs of commercial activities under the collaboration agreement is recorded as a component of Selling, general and administrative expenses in the unaudited condensed consolidated statement of earnings (loss). Refer to Note 15, Collaboration Agreements.
Insurance Recoveries
Insurance Recoveries
The Company has several policies with third-party insurers that provide for the recovery of certain costs incurred by the Company. The Company records its rights to insurance recoveries as a receivable when the respective costs are reimbursable under applicable insurance policies, it is probable that such costs will be reimbursed, and reimbursement can be reasonably estimated. As such, the Company estimates the percentage of costs that will be reimbursed by the insurance provider to determine the proper amount to record for the insurance receivable.
Recently Issued Accounting Pronouncements
Recently Issued Accounting Pronouncements
New Accounting Pronouncements Not Yet Adopted
ASU 2024-03, Disaggregation of Income Statement Expenses (Topic 220) - The new standard, issued in November 2024, requires additional disclosure in tabular format, about the nature of specific types of expense captions presented on the face of the income statement as well as disclosures about selling expenses. The new standard does not change the requirements for the presentation of expenses on the face of the income statement. The standard is effective with annual periods beginning after December 15, 2026. Early adoption and retrospective application are permitted. The Company plans to adopt the guidance for the fiscal year ending December 31, 2027. We expect ASU 2024-03 to require additional disclosures in the notes to our consolidated financial statements. The Company is currently evaluating the effects the adoption of this guidance will have on the consolidated financial statements.
ASU 2025-06, Intangibles-Goodwill and Other-Internal-Use Software (Subtopic 350-40): Targeted Improvements to the Accounting for Internal-Use Software (ASU 2025-06) - The new standard, issued in September 2025, modernizes the accounting for internal-use software. ASU 2025-06 removes all references to software development stages and requires capitalization of software costs when management has committed to the software project and it is probable the software will be completed and perform its intended use. The Company plans to adopt the guidance for the fiscal year ending December 31, 2028. The Company is currently evaluating the timing and method of its adoption of ASU 2025-06 and the effects the adoption of this guidance will have on the consolidated financial statements.
ASU 2025-11, Interim Reporting - Narrow-Scope Improvements (Topic 270) - The new standard, issued in December 2025, clarifies the interim reporting requirements by improving navigability of Topic 270 and more clearly specifies what disclosures are required in an interim reporting period. It is not intended to significantly change interim reporting or expand or reduce interim disclosure requirements. The standard is effective for interim reporting periods in fiscal years beginning after December 15, 2027. Early adoption is permitted. The Company plans to adopt the guidance for the fiscal year ending December 31, 2028. The Company is currently evaluating the effects the adoption of this guidance will have on the consolidated financial statements.
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v3.26.3
Goodwill and Intangible Assets, Net - Narrative (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2026
Jun. 30, 2026
Sep. 30, 2025
Sep. 30, 2026
Sep. 30, 2025
Jul. 31, 2025
Feb. 28, 2025
Intangible Asset, Finite-Lived [Line Items]              
Amortization of intangible assets $ 23,221   $ 24,325 $ 74,198 $ 64,930    
Impairment charges $ 1,541 $ 54,900 $ 0 56,460 $ 0    
USWM Acquisition              
Intangible Asset, Finite-Lived [Line Items]              
Estimated Useful Lives (in years)             10 years
Sage Acquisition              
Intangible Asset, Finite-Lived [Line Items]              
Amortization of intangible assets       $ 300      
Estimated Useful Lives (in years)           8 years  
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v3.26.3
Share-Based Payments
9 Months Ended
Sep. 30, 2026
Share-Based Payment Arrangement [Abstract]  
Share-Based Payments Share-Based Payments
Employee Stock Purchase Plan
In the fourth quarter of 2026, the Company's Board of Directors approved the termination of the Second Amended and Restated 2012 Employee Stock Purchase Plan (ESPP). The termination will become effective on, to be conditioned upon, the consummation of the Merger. The current option period shall end on September 30, 2026, and September 30, 2026 shall be designated as, and treated as, the “Exercise Date” for the current option period in lieu of December 31, 2026. Shares issuable under the current offering period will be issued in accordance with the terms of the plan, and no additional offering periods will commence thereafter absent further action by the Company's Board of Directors.
Equity Incentive Plan
The Company has adopted the Supernus Pharmaceuticals, Inc. 2021 Equity Incentive Plan (2021 Plan) which was approved by the stockholders in June 2021. The 2021 Plan is the successor to, and replaced the 2012 Equity Incentive Plan, as amended (the 2012 Plan). The 2021 Plan is administered by the Company's Board of Directors and the Company's Compensation Committee of the Board. The 2021 Plan provides for the grant of stock options and certain other equity awards, including: stock appreciation rights (SARs); restricted and unrestricted stock; stock units; performance awards; cash awards; and other awards that are convertible into or otherwise based on the Company's common stock, to the Company's key employees, directors, consultants, and advisors. In June 2026, the Company's shareholders approved, and the Company has adopted, the Amended and Restated 2021 Equity Incentive Plan (the Amended 2021 Plan) to increase the number of shares of the Company's common stock available
for issuance under the 2021 Plan by 4,000,000 shares. The maximum number of shares that can be issued under the Amended 2021 Plan is 19,012,893 shares of the Company's common stock which includes the (i) 4,000,000 shares added pursuant to the adoption of the Amended 2021 Plan, (ii) the number of shares that remain available to be issued or transferred pursuant to awards under the 2021 Equity Incentive Plan as of the adoption date of the Amended 2021 Plan, and (iii) the number of shares that have already been issued or transferred pursuant to awards under the 2021 Plan prior to the approval by the Company’s stockholders of the Amended 2021 Plan.
Share-based compensation expense is as follows (dollars in thousands):
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)(unaudited)
Research and development$1,525 $1,446 $4,449 $4,337 
Selling, general and administrative(a)
7,408 29,299 21,604 41,983 
Total$8,933 $30,745 $26,053 $46,320 
(a) The prior period includes $22.9 million of compensation expense related to the acceleration of certain Sage equity awards in connection with the Sage Acquisition in July 2025.
The Company has $12.3 million of unrecognized compensation expense related to CVRs granted to holders of the accelerated Sage equity awards as of September 30, 2026. This unrecognized compensation expense will be recognized if and when the milestones associated with the CVRs become probable of achievement.
Stock Options
The following table summarizes stock option activities:
Number of
Options
Weighted
Average
Exercise Price
Weighted
Average
Remaining
Contractual
Term (in years)
Outstanding, December 31, 20256,343,009 $32.63 6.3
Granted 988,592 $49.93 
Exercised (565,366)$31.00 
Forfeited (124,726)$39.06 
Outstanding, September 30, 2026 (unaudited)6,641,509 $35.22 6.2
As of September 30, 2026 (unaudited):
Vested and expected to vest6,641,509 $35.22 6.2
Exercisable 4,053,054 $32.46 4.8
As of December 31, 2025:
Vested and expected to vest6,343,009 $32.63 6.3
Exercisable3,636,073 $32.08 4.8
Restricted Stock Units
The following table summarizes restricted stock unit (RSU) activities:
Number of
RSUs
Weighted Average
Grant Date Fair Value per Share
Nonvested, December 31, 2025396,693 $32.98 
Granted122,609 $50.20 
Vested(165,678)$33.43 
Forfeited(11,375)$37.89 
Nonvested, September 30, 2026 (unaudited)342,249 $38.77 
Performance Share Units
The following table summarizes performance share unit (PSU) activities:
Number of PSUsWeighted
Average
Grant Date Fair Value per Share
Nonvested, December 31, 2025390,496 $30.80 
Granted236,466 $47.73 
Vested(103,989)$29.43 
Forfeited(57,590)$28.33 
Nonvested, September 30, 2026 (unaudited)465,383$40.01 
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v3.26.3
Income Tax Expense (Benefit)
9 Months Ended
Sep. 30, 2026
Income Tax Disclosure [Abstract]  
Income Tax Expense (Benefit) Income Tax Expense (Benefit)
The following table provides information regarding the Company's income tax expense (benefit) for the three and nine months ended September 30, 2026 and 2025 (dollars in thousands):
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)(unaudited)
Income tax expense (benefit)$1,796 $(12,837)$(1,138)$(12,671)
Effective tax rate7.9 %22.2 %2.8 %26.9 %

Income tax expense (benefit) was an expense of $1.8 million (7.9% effective tax rate) and a benefit of $1.1 million (2.8% effective tax rate) for the three and nine months ended September 30, 2026, as compared to an income tax benefit of $12.8 million (22.2% effective tax rate) and income tax benefit of $12.7 million (26.9% effective tax rate) for the three and nine months ended September 30, 2025. The change in both periods for income tax expense (benefit) and effective income tax rate was primarily due to the change in forecasted and year-to-date earnings and the impact of discrete tax benefits as compared to the same period in 2025.

The Company's effective income tax rate for the three and nine months ended September 30, 2026 varies from the statutory federal tax rate in the United States (U.S. federal tax rate) of 21% primarily due to the change in pretax book income (loss), non-deductible executive compensation, milestone payments, state taxes, other non-deductible permanent items offset by the impact of discrete benefit recorded during the period. The Company's effective income tax rate for the three months ended September 30, 2025 varies from the statutory U.S. federal tax rate primarily due to state taxes and non-deductible transaction costs, offset by tax benefits related to research and development tax credits. The Company's effective income tax rate for the nine months ended September 30, 2025 varies from the statutory U.S. federal tax rate primarily due to state taxes and non-deductible transaction costs, offset by tax benefits related to a state tax refund and research and development tax credits.

The annual forecasted earnings represent the Company's best estimate as of September 30, 2026 and 2025, are subject to change and could have a material impact on the effective tax rate in subsequent periods. ASC 740, Income Taxes (ASC 740), requires the Company to estimate the annual effective income tax rate for the full year and apply it to pre-tax income (loss) for each interim period, taking into account year-to-date amounts and projected results for the full year.

As of September 30, 2026 and December 31, 2025, the Company had income tax receivable of $24.9 million and $38.4 million, respectively, which is classified as Prepaid expenses and other current assets on the condensed consolidated balance sheets.
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Leases - Schedule of Leases Balance Sheet Information (Details) - USD ($)
$ in Thousands
Sep. 30, 2026
Dec. 31, 2025
Assets    
Operating lease assets $ 23,059 $ 26,712
Operating lease assets, location Other assets Other assets
Liabilities    
Operating lease liabilities, current portion $ 7,620 $ 10,612
Operating lease liabilities, current portion, location Accounts payable and accrued liabilities Accounts payable and accrued liabilities
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9 Months Ended 12 Months Ended
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Beginning balance $ 124,882 $ 117,019
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Earnings (Loss) per Share - Schedule of Computation of Basic and Diluted Earnings per Share (Details) - USD ($)
$ / shares in Units, $ in Thousands
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Sep. 30, 2026
Jun. 30, 2026
Mar. 31, 2026
Sep. 30, 2025
Jun. 30, 2025
Mar. 31, 2025
Sep. 30, 2026
Sep. 30, 2025
Numerator:                
Net loss $ 20,913 $ (58,371) $ (2,293) $ (45,117) $ 22,499 $ (11,827) $ (39,751) $ (34,445)
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Numerator for dilutive earnings (loss) per share $ 20,913     $ (45,117)     $ (39,751) $ (34,445)
Denominator:                
Weighted average shares outstanding, basic (in shares) 58,202,474     56,552,741     57,975,499 56,133,918
Effect of dilutive securities:                
Stock options and stock awards (in shares) 1,268,547     0     0 0
Weighted average shares outstanding, diluted (in shares) 59,471,021     56,552,741     57,975,499 56,133,918
Earnings (loss) per share, basic (in dollars per share) $ 0.36     $ (0.80)     $ (0.69) $ (0.61)
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v3.26.3
Composition of Other Balance Sheet Items
9 Months Ended
Sep. 30, 2026
Organization, Consolidation and Presentation of Financial Statements [Abstract]  
Composition of Other Balance Sheet Items Composition of Other Balance Sheet Items
The following details the composition of other balance sheet items (dollars in thousands for amounts in tables):
Inventories, Net
September 30,
2026
December 31,
2025
(unaudited)
Raw materials$29,120 $31,833 
Work in process24,843 29,436 
Finished goods33,149 21,116 
Total$87,112 $82,385 
Inventories, net as reported on the condensed consolidated balance sheets are as follows (dollars in thousands):
Balance Sheet ClassificationSeptember 30, 2026December 31, 2025
(unaudited)
Current inventory
Inventories, net
$87,112 $82,385 
Noncurrent inventory
Other Assets
26,131 30,095 
Total $113,243 $112,480 
Property and Equipment, Net
September 30,
2026
December 31,
2025
(unaudited)
Lab equipment and furniture$14,538 $14,041 
Leasehold improvements13,052 13,052 
Software951 871 
Computer equipment1,052 831 
Subtotal29,593 28,795 
Less accumulated depreciation and amortization(19,572)(18,264)
Property and equipment, net$10,021 $10,531 
Depreciation and amortization expense on property and equipment was approximately $0.4 million and $1.3 million for three and nine months ended September 30, 2026, respectively, and $0.5 million and $1.6 million for the three and nine months ended September 30, 2025, respectively.
Accounts Payable and Accrued Liabilities
September 30,
2026
December 31,
2025
(unaudited)
Accrued manufacturing expenses$29,874 $25,608 
Accrued compensation, benefits, & related accruals27,596 29,446 
Accrued sales & marketing14,220 16,665 
Operating lease liabilities, current portion(a)
7,620 10,612 
Accounts payable8,517 2,677 
Accrued R&D expenses6,592 7,299 
Accrued royalties(b)
622 2,403 
Other accrued expenses14,095 13,090 
Total$109,136 $107,800 
_______________________________
(a) Refer to Note 13, Leases.
(b) Refer to Note 17, Commitments and Contingencies.
Accrued Product Returns and Rebates
September 30,
2026
December 31,
2025
(unaudited)
Accrued product rebates$131,537 $123,297 
Accrued product returns33,811 37,800 
Total$165,348 $161,097 
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Earnings (Loss) per Share - Schedule of Common Stock Equivalents Excluded in the Calculation of Diluted Earnings per Share (Details) - shares
3 Months Ended 9 Months Ended
Sep. 30, 2026
Sep. 30, 2025
Sep. 30, 2026
Sep. 30, 2025
Stock options and stock awards        
Income per share        
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$ in Thousands
Sep. 30, 2026
Dec. 31, 2025
Organization, Consolidation and Presentation of Financial Statements [Abstract]    
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Accrued compensation, benefits, & related accruals 27,596 29,446
Accrued sales & marketing 14,220 16,665
Operating lease liabilities, current portion 7,620 10,612
Accounts payable 8,517 2,677
Accrued R&D expenses 6,592 7,299
Accrued royalties 622 2,403
Other accrued expenses 14,095 13,090
Total $ 109,136 $ 107,800
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v3.26.3
Segment Reporting
9 Months Ended
Sep. 30, 2026
Segment Reporting [Abstract]  
Segment Reporting Segment Reporting
The Company operates in one operating segment and therefore has only one reportable segment. The Company derives revenue primarily from sales of its commercial products in the U.S.

The Company's chief operating decision maker (CODM) is the chief executive officer. The Company manages the business activities on a consolidated basis. The CODM assesses performance of the Company, decides how to allocate resources based on net earnings (loss), which is reported in the condensed consolidated statement of earnings (loss) as net earnings (loss), and allocates resources on a consolidated basis. The CODM uses net earnings (loss) to decide whether to reinvest profits into the Company's current products or into other research and development initiatives for the Company's product candidates. Net earnings (loss) is also used to monitor budget versus actual results.

The measure of the reportable segment assets is reported on the balance sheet as total assets.
The following table shows the segment revenue, significant segment expenses and net earnings (dollars in thousands):
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)(unaudited)
Total revenues
$226,771 $192,103 $653,534 $507,380 
Less: Significant segment expenses:
Cost of revenues27,018 18,965 84,078 51,555 
Selling expenses
68,736 58,386 203,924 145,398 
Marketing expenses
21,778 18,672 66,356 60,068 
General and administrative expenses(a)
37,542 33,114 116,586 86,833 
Research and development expenses


Acquisition-related expenses— 69,506 — 70,874 
External development program expenses:
ONAPGO
58 352 834 1,613 
SPN-8203,507 1,111 8,324 8,073 
SPN-817(b)
4,215 4,872 27,715 11,889 
SPN-4431,113 773 2,159 1,799 
Qelbree1,899 3,168 6,480 9,805 
ZURZUVAE70 1,385 225 1,385 
Early-stage programs and other expenses
4,885 4,400 16,552 10,066 
Total external development program expenses
15,747 16,061 62,289 44,630 
Internal employee-related expenses
10,009 13,305 32,368 33,778 
Total research and development expenses
25,756 29,366 94,657 78,408 
Other segment items(c)
25,028 9,211 127,684 48,689 
Net earnings (loss)$20,913 $(45,117)$(39,751)$(34,445)
(a) Excludes Sage Acquisition related expenses which are presented in the separate line item, Acquisition-related expenses, in the table above.
(b) Includes amount related to Biscayne amendment. Refer to Note 17, Commitments and Contingencies.
(c) Other segment items include amortization of intangible assets, impairment charges, contingent consideration loss, net interest and other income, interest expense, and income tax expense (benefit) whose amounts are disclosed in the condensed consolidated statement of earnings (loss).
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v3.26.3
Contingent Consideration (Tables)
9 Months Ended
Sep. 30, 2026
Business Combination, Asset Acquisition, Transaction between Entities under Common Control, and Joint Venture Formation [Abstract]  
Schedule of Business Combination, Contingent Consideration
The following table sets forth the contingent consideration liabilities (dollars in thousands):
September 30, 2026December 31, 2025
(unaudited)
Reported under the following captions in the condensed consolidated balance sheets:
Contingent consideration, current portion$— $31,052 
Contingent consideration, long-term206 206 
Total$206 $31,258 
Schedule of Reconciliation of the Beginning and Ending Balances Related to the Contingent Consideration
The following tables provide a reconciliation of the beginning and ending balances related to the contingent consideration liability for the USWM Acquisition and Sage Acquisition (dollars in thousands):
USWM AcquisitionSage AcquisitionTotal
Balance, December 31, 2025$— $31,258 $31,258 
Change in fair value recognized in earnings — 2,391 2,391 
Milestone payments — (33,443)(33,443)
Balance at September 30, 2026 (unaudited)$— $206 $206 
USWM AcquisitionSage AcquisitionTotal
Balance, December 31, 2024$47,340 $— $47,340 
Contingent consideration from Sage Acquisition— 11,448 $11,448 
Change in fair value recognized in earnings7,660 — 7,660 
Milestone payments (27,295)— (27,295)
Reclassification to Other Current Liabilities
(27,705)(27,705)
Balance at September 30, 2025 (unaudited)$— $11,448 $11,448 
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v3.26.3
Fair Value of Financial Instruments
9 Months Ended
Sep. 30, 2026
Fair Value Disclosures [Abstract]  
Fair Value of Financial Instruments Fair Value of Financial Instruments
The fair value of an asset or liability represents the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between unrelated market participants.
The Company reports the fair value of assets and liabilities using a three level measurement hierarchy that prioritizes the inputs used to measure fair value. Fair value hierarchy consists of the following three levels:
•Level 1—Valuations based on unadjusted quoted prices in active markets that are accessible at measurement date for identical assets.
•Level 2—Valuations based on quoted prices for similar assets or liabilities in active markets, quoted prices for identical or similar assets or liabilities in markets that are not active and model-based valuations in which all significant inputs are observable in the market, either directly or indirectly (e.g., interest rates; yield curves).
•Level 3—Valuations using significant inputs that are unobservable in the market and inputs that reflect the Company's own assumptions. These are based on the best information available, including the Company's own data.
Financial Assets and Liabilities Recorded at Fair Value
The Company's financial assets and liabilities that are required to be measured at fair value on a recurring basis are as follows (dollars in thousands):
Fair Value Measurements as of September 30, 2026 (unaudited)
Total
Level 1 Level 2Level 3
Assets:
Cash and cash equivalents
Cash$59,213 $59,213 $— $— 
Money market funds116,671 116,671 — — 
Marketable securities
Corporate debt securities183,575 — 183,575 — 
U.S government agency securities— —— —
Other noncurrent assets
Marketable securities - restricted (SERP)767 32 735 — 
Restricted cash
1,450 1,450 — — 
Total assets at fair value$361,676 $177,366 $184,310 $— 
Liabilities:
Contingent consideration$206 $— $— $206 
Total liabilities at fair value$206 $— $— $206 
Fair Value Measurements as of December 31, 2025
Total
Level 1 Level 2Level 3
Assets:
Cash and cash equivalents
Cash$56,371 $56,371 $— $— 
Money market funds72,077 72,077 — — 
Marketable securities
Corporate debt securities164,519 — 164,519 — 
Municipal debt securities14,716 —14,716 —
U.S. government agency debt securities987 —987 —
Other noncurrent assets
Marketable securities - restricted (SERP)705 27 678 — 
Restricted Cash1,450 1,450 — $— 
Total assets at fair value$310,825 $129,925 $180,900 $— 
Liabilities:
Contingent consideration$31,258 $— $— $31,258 
Total liabilities at fair value$31,258 $— $— $31,258 
Other Financial Instruments
The carrying amounts of other financial instruments, including accounts receivable, accounts payable, and accrued expenses approximate fair value due to their short-term maturities.
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v3.26.3
Condensed Consolidated Statements of Changes in Stockholders’ Equity - USD ($)
$ in Thousands
Total
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Accumulated Other Comprehensive Earnings (Loss)
Retained Earnings
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Increase (Decrease) in Stockholders' Equity          
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Issuance of common stock related to employee stock purchase plan and share-based awards, net of taxes withheld (1,299)   (1,299)    
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Issuance of common stock related to employee stock purchase plan and share-based awards, net of taxes withheld (in shares)   130,112      
Issuance of common stock related to employee stock purchase plan and share-based awards, net of taxes withheld 3,230   3,230    
Net earnings (loss) 22,499       22,499
Unrealized gain (loss) on marketable securities, net of tax (41)     (41)  
Ending balance (in shares) at Jun. 30, 2025   56,119,360      
Ending balance at Jun. 30, 2025 1,063,900 $ 56 496,946 (200) 567,098
Increase (Decrease) in Stockholders' Equity          
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Issuance of common stock related to employee stock purchase plan and share-based awards, net of taxes withheld (in shares)   999,793      
Issuance of common stock related to employee stock purchase plan and share-based awards, net of taxes withheld 22,930 $ 1 22,929    
Net earnings (loss) (45,117)       (45,117)
Unrealized gain (loss) on marketable securities, net of tax 129     129  
Ending balance (in shares) at Sep. 30, 2025   57,119,153      
Ending balance at Sep. 30, 2025 $ 1,049,667 $ 57 527,700 (71) 521,981
Beginning balance (in shares) at Dec. 31, 2025 57,457,462 57,457,462      
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Increase (Decrease) in Stockholders' Equity          
Share-based compensation expense related to employee stock purchase plan and share-based awards 8,480   8,480    
Issuance of common stock related to employee stock purchase plan and share-based awards, net of taxes withheld (in shares)   582,259      
Issuance of common stock related to employee stock purchase plan and share-based awards, net of taxes withheld 9,115 $ 1 9,114    
Net earnings (loss) (2,293)       (2,293)
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Ending balance (in shares) at Mar. 31, 2026   58,039,721      
Ending balance at Mar. 31, 2026 $ 1,076,805 $ 58 561,419 (255) 515,583
Beginning balance (in shares) at Dec. 31, 2025 57,457,462 57,457,462      
Beginning balance at Dec. 31, 2025 $ 1,061,714 $ 57 543,825 (44) 517,876
Increase (Decrease) in Stockholders' Equity          
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Unrealized gain (loss) on marketable securities, net of tax $ (236)        
Ending balance (in shares) at Sep. 30, 2026 58,254,131 58,254,131      
Ending balance at Sep. 30, 2026 $ 1,062,478 $ 58 584,575 (280) 478,125
Beginning balance (in shares) at Mar. 31, 2026   58,039,721      
Beginning balance at Mar. 31, 2026 1,076,805 $ 58 561,419 (255) 515,583
Increase (Decrease) in Stockholders' Equity          
Share-based compensation expense related to employee stock purchase plan and share-based awards 8,640   8,640    
Issuance of common stock related to employee stock purchase plan and share-based awards, net of taxes withheld (in shares)   124,631      
Issuance of common stock related to employee stock purchase plan and share-based awards, net of taxes withheld 4,035   4,035    
Net earnings (loss) (58,371)       (58,371)
Unrealized gain (loss) on marketable securities, net of tax 117     117  
Ending balance (in shares) at Jun. 30, 2026   58,164,352      
Ending balance at Jun. 30, 2026 1,031,226 $ 58 574,094 (138) 457,212
Increase (Decrease) in Stockholders' Equity          
Share-based compensation expense related to employee stock purchase plan and share-based awards 8,933   8,933    
Issuance of common stock related to employee stock purchase plan and share-based awards, net of taxes withheld (in shares)   89,779      
Issuance of common stock related to employee stock purchase plan and share-based awards, net of taxes withheld 1,548   1,548    
Net earnings (loss) 20,913       20,913
Unrealized gain (loss) on marketable securities, net of tax $ (142)     (142)  
Ending balance (in shares) at Sep. 30, 2026 58,254,131 58,254,131      
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v3.26.3
Contingent Consideration
9 Months Ended
Sep. 30, 2026
Business Combination, Asset Acquisition, Transaction between Entities under Common Control, and Joint Venture Formation [Abstract]  
Contingent Consideration Contingent Consideration
The following table sets forth the contingent consideration liabilities (dollars in thousands):
September 30, 2026December 31, 2025
(unaudited)
Reported under the following captions in the condensed consolidated balance sheets:
Contingent consideration, current portion$— $31,052 
Contingent consideration, long-term206 206 
Total$206 $31,258 
The Company's contingent consideration liabilities as of September 30, 2026 and December 31, 2025 are related to the Sage Acquisition in 2025.
Sage Contingent Consideration
At the Sage Acquisition Date, the contingent consideration liabilities are measured using either a market participant approach with both implied fair value from the stock price combined with a Monte Carlo simulation or income approach. At September 30, 2026, the contingent consideration are measured using the income approach. The Company classifies contingent consideration liabilities as Level 3 fair value measurements in the period where significant unobservable inputs were used to estimate fair value. These reflect the inputs and assumptions the Company believes would be made by market participants. Changes in any of those inputs together or in isolation may result in significantly lower or higher fair value measurement. The key assumptions considered include the estimated amount and timing of projected revenues, volatility, probability of milestone achievement, estimated discount rates, and risk-free interest rate. The change in fair value is reported on the condensed consolidated statement of earnings (loss) in Contingent consideration loss.
On July 31, 2025, the Company completed the Sage Acquisition. The Sage Acquisition included payment of one contingent value right (Sage CVR) which represents the right to receive up to $3.50, which is governed by the terms of a contingent value rights agreement entered into between the Company and CVR Agent (Sage CVR Agreement), in cash, less any applicable withholding taxes and without interest.
Subject to the terms of the Sage CVR Agreement, (1) $1.00 per share would be payable if in any calendar year between closing and end of 2027, annual net sales (as defined in the Sage CVR Agreement) of ZURZUVAE allocable to Supernus or any of its affiliates reach $250 million or more in the U.S., (2) $1.00 per share would be payable if in any calendar year between closing and end of 2028, annual net sales (as defined in the Sage CVR Agreement) of ZURZUVAE allocable to Supernus or any of its affiliates reach $300 million or more in the U.S., (3) $1.00 per share would be payable if in any calendar year between closing and end of 2030, annual net sales (as defined in the Sage CVR Agreement) of ZURZUVAE allocable to Supernus or any of its affiliates reach $375 million or more in the U.S., and (4) $0.50 per share would be payable upon the first commercial sale in Japan to a third-party customer after regulatory approval for ZURZUVAE for the treatment of MDD in Japan by June 30, 2026. The maximum amount payable with respect to a CVR issued in respect to each Share is $3.50, an aggregate of approximately $234 million.
ZURZUVAE received regulatory approval for the treatment of MDD in Japan in December 2025. In March 2026, Shionogi announced the successful commercial launch of a product containing zuranolone for the treatment of MDD in Japan. As such, the CVR became due and payable. The Company paid the full milestone amount of $33.4 million in June 2026 and thus, derecognized the liability. The possible outcomes for the remaining unmet milestones range from $0 to $201 million on an undiscounted basis as of September 30, 2026.
USWM Contingent Consideration
On June 9, 2020 (the USWM Closing Date), the Company completed its acquisition of all the outstanding equity of USWM Enterprises, LLC (USWM Enterprises) (USWM Acquisition). The USWM Acquisition included potential additional contingent consideration payments for regulatory and development milestones and sales-based milestones. At December 31, 2024, there were two remaining outstanding milestones, one related to the approval of ONAPGO and the other related to the commercial launch of ONAPGO. Both milestones were met in 2025 and the liability was accreted to the milestone amounts due resulting in the recognition of $7.7 million change in fair value of contingent consideration. In February 2025, the Company paid the $25 million milestone related to the FDA's approval of ONAPGO in February 2025. ONAPGO was launched in April 2025 and the $30 million milestone payment related to the commercial launch of ONAPGO, subject to certain holdbacks as permitted
under the Sale and Purchase Agreement Relating to USWM Enterprises, LLC, dated April 28, 2020, by and between US WorldMeds Partners, LLC and Supernus Pharmaceuticals, Inc., (USWM Sale and Purchase Agreement) became due and payable. Of the $30 million, the Company paid $2.3 million in the second quarter of 2025 and the remaining amount held was reclassified to Other current liabilities in the condensed consolidated balance sheet as the milestone had been met but payment remains subject to certain holdbacks permitted under the USWM Sale and Purchase Agreement. Following a proceeding in the Superior Court of the State of Delaware, during the second quarter of 2026, the Company was ordered to pay USWM the held back principal, as well as accrued interest and legal expenses. In the third quarter of 2026, the Company paid $25.1 million to USWM, which represents $29.1 million of the held back principal and interest, offset against $4.0 million payment from USWM to Supernus in respect of certain insurance recoveries.
Change in the Fair Value of Contingent Consideration
The following tables provide a reconciliation of the beginning and ending balances related to the contingent consideration liability for the USWM Acquisition and Sage Acquisition (dollars in thousands):
USWM AcquisitionSage AcquisitionTotal
Balance, December 31, 2025$— $31,258 $31,258 
Change in fair value recognized in earnings — 2,391 2,391 
Milestone payments — (33,443)(33,443)
Balance at September 30, 2026 (unaudited)$— $206 $206 
USWM AcquisitionSage AcquisitionTotal
Balance, December 31, 2024$47,340 $— $47,340 
Contingent consideration from Sage Acquisition— 11,448 $11,448 
Change in fair value recognized in earnings7,660 — 7,660 
Milestone payments (27,295)— (27,295)
Reclassification to Other Current Liabilities
(27,705)(27,705)
Balance at September 30, 2025 (unaudited)$— $11,448 $11,448 
The Company recorded the following changes in fair value of the contingent consideration liability for the USWM milestones:
•No expense was recorded during the three and nine months ended September 30, 2026. No expense was recorded during the three months ended September 30, 2025. The Company recorded a $7.7 million expense due to the change in fair value of contingent consideration liabilities for the USWM milestones for the nine months ended September 30, 2025. The change in fair value of contingent consideration was primarily due to accretion to the full milestone payment amount with the achievement of the milestones.
The Company recorded the following changes in the fair value of contingent consideration liability for the Sage CVRs:
•No change in fair value was recorded during the three months ended September 30, 2026. $2.4 million change in fair value was recorded during the nine months ended September 30, 2026 due to the achievement of the milestone related to the first commercial sale in Japan to a third-party customer after regulatory approval for ZURZUVAE for the treatment of major depressive disorder (MDD) in Japan by June 30, 2026. The Company recorded a contingent consideration liability of $11.4 million at Sage Closing Date. No change in fair value was recorded during the three and nine months ended September 30, 2025 given the proximity of the Sage Acquisition to the reporting period end date.
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v3.26.3
Disaggregated Revenues
9 Months Ended
Sep. 30, 2026
Disaggregation of Revenue [Abstract]  
Disaggregated Revenues Disaggregated Revenues
The following table provides information regarding total revenues (dollars in thousands):
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)(unaudited)
Net product sales
Qelbree$90,824 $81,416 $257,906 $223,708 
GOCOVRI42,650 40,849 115,420 108,198 
ONAPGO17,075 6,806 38,996 8,410 
Trokendi XR10,213 10,043 28,103 34,037 
Oxtellar XR7,957 12,016 24,161 33,851 
APOKYN6,490 10,387 20,541 38,183 
Other(a)
3,367 7,025 9,915 22,138 
Total net product sales178,576 168,542 495,042 468,525 
Collaboration revenue (ZURZUVAE)(b)
41,697 20,164 104,690 20,164 
Royalty, licensing, and other revenues6,498 3,397 53,802 18,691 
Total revenues$226,771 $192,103 $653,534 $507,380 
___________________________________________
(a) Includes net product sales of MYOBLOC, XADAGO and Osmolex ER.
(b) Includes the Company's proportionate share of net sales of ZURZUVAE.
The Company recognized $20.0 million of licensing revenue in the nine months ended September 30, 2026 related to the achievement of a commercial milestone under the Company's collaboration agreement with Shionogi.
Adjustments related to prior year sales for the nine months ended September 30, 2026 were approximately 1% of net product sales. Adjustments related to prior year sales for the nine months ended September 30, 2025 were approximately 4% of net product sales. In 2025, the Company had favorable actual returns experience and as a result, the Company changed its estimated provision for product returns based on the most recent experience. Adjustments related to prior year sales for the nine months ended September 30, 2025 were primarily attributable to Qelbree.
We do not currently own or operate manufacturing facilities for the commercial production of any of our commercial products. We currently depend on third-party clinical manufacturing organizations (CMOs), who offer a comprehensive range of contract manufacturing and packaging services, in various countries for the supply of active product ingredients (API), and finished goods for our commercial products. For most of our commercial products, we rely on single source suppliers to produce and package final dosage forms for our products and raw materials, including API.

On November 4, 2025, the Company announced that due to stronger than expected demand for ONAPGO, supplier constraints were impacting the Company's ability to fully meet this demand. ONAPGO is manufactured in Europe, supplied to us by our ONAPGO licensing partner, and packaged in the U.S. by a third-party CMO. The Company relies on single source suppliers to produce and package final dosage forms for ONAPGO. In February 2026, the Company announced that it has made progress in securing additional product supply of ONAPGO from the current supplier and, as a result, has resumed new patient initiation. In October 2026 the Company submitted a supplemental New Drug Application (sNDA) to the FDA for a second supplier for ONAPGO, with potential FDA approval by mid-year 2027. Any changes in any of the suppliers would require regulatory approval which could cause a further delay in manufacturing and a possible loss of sales, which could affect future operating results adversely.
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v3.26.3
Composition of Other Balance Sheet Items (Tables)
9 Months Ended
Sep. 30, 2026
Organization, Consolidation and Presentation of Financial Statements [Abstract]  
Schedule of Inventory, Current
September 30,
2026
December 31,
2025
(unaudited)
Raw materials$29,120 $31,833 
Work in process24,843 29,436 
Finished goods33,149 21,116 
Total$87,112 $82,385 
Schedule of Inventory, Current and Noncurrent
Inventories, net as reported on the condensed consolidated balance sheets are as follows (dollars in thousands):
Balance Sheet ClassificationSeptember 30, 2026December 31, 2025
(unaudited)
Current inventory
Inventories, net
$87,112 $82,385 
Noncurrent inventory
Other Assets
26,131 30,095 
Total $113,243 $112,480 
Schedule of Property and Equipment Property and Equipment, Net
September 30,
2026
December 31,
2025
(unaudited)
Lab equipment and furniture$14,538 $14,041 
Leasehold improvements13,052 13,052 
Software951 871 
Computer equipment1,052 831 
Subtotal29,593 28,795 
Less accumulated depreciation and amortization(19,572)(18,264)
Property and equipment, net$10,021 $10,531 
Schedule of Accounts Payable and Accrued Liabilities
Accounts Payable and Accrued Liabilities
September 30,
2026
December 31,
2025
(unaudited)
Accrued manufacturing expenses$29,874 $25,608 
Accrued compensation, benefits, & related accruals27,596 29,446 
Accrued sales & marketing14,220 16,665 
Operating lease liabilities, current portion(a)
7,620 10,612 
Accounts payable8,517 2,677 
Accrued R&D expenses6,592 7,299 
Accrued royalties(b)
622 2,403 
Other accrued expenses14,095 13,090 
Total$109,136 $107,800 
_______________________________
(a) Refer to Note 13, Leases.
(b) Refer to Note 17, Commitments and Contingencies.
Schedule of Accrued Sales Deductions
Accrued Product Returns and Rebates
September 30,
2026
December 31,
2025
(unaudited)
Accrued product rebates$131,537 $123,297 
Accrued product returns33,811 37,800 
Total$165,348 $161,097 
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Composition of Other Balance Sheet Items - Schedule of Inventory as Reported on Balance Sheet (Details) - USD ($)
$ in Thousands
Sep. 30, 2026
Dec. 31, 2025
Organization, Consolidation and Presentation of Financial Statements [Abstract]    
Current inventory $ 87,112 $ 82,385
Noncurrent inventory 26,131 30,095
Total $ 113,243 $ 112,480
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v3.26.3
Collaboration Agreements (Tables)
9 Months Ended
Sep. 30, 2026
Organization, Consolidation and Presentation of Financial Statements [Abstract]  
Schedule of Revenue, Cost of Revenues, and Expense The following table summarizes the Company’s proportionate share of the activity under the Biogen Collaboration Agreement:
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)
(unaudited)
Collaboration revenue (ZURZUVAE)
$41,697 $20,164 $104,690 $20,164 
Cost of revenues
641 434 2,967 434 
Research and development expenses
504 (928)1,797 (928)
Selling, general and administrative expenses
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v3.26.3
Insider Trading Arrangements
3 Months Ended
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shares
Trading Arrangements, by Individual  
Material Terms of Trading Arrangement
The table below lists the insider trading arrangements adopted or terminated during the third quarter of 2026:
Name and Title of Director or Officer
Rule 10b5-1 Trading Arrangement(1)
Trading Arrangement Adopted or TerminatedDate of Adoption or TerminationDuration of Trading ArrangementAggregate Number of Securities to be Purchased Pursuant to Trading ArrangementAggregate Number of Securities to be Sold Pursuant to Trading Arrangement
Jack Khattar

President, Chief Executive Officer and Director
YesTerminatedAugust 12, 2026First Transaction Date through February 24, 2027—297,500
Charles Newhall

Director
YesTerminatedAugust 12, 2026First Transaction Date through June 15, 2027—5,000
William Todd Horich

Senior Vice President, Chief Commercial Officer
YesTerminatedAugust 12, 2026First Transaction Date through March 12, 2027—44,000
____________________________________
(1) Indicates whether the trading arrangement is intended to satisfy the affirmative defense conditions of Rule 10b5-1(c).
Rule 10b5-1 Arrangement Adopted false
Non-Rule 10b5-1 Arrangement Adopted false
Non-Rule 10b5-1 Arrangement Terminated false
Jack Khattar [Member]  
Trading Arrangements, by Individual  
Name Jack Khattar
Title President, Chief Executive Officer and Director
Rule 10b5-1 Arrangement Terminated true
Termination Date August 12, 2026
Aggregate Available 297,500
Charles Newhall [Member]  
Trading Arrangements, by Individual  
Name Charles Newhall
Title Director
Rule 10b5-1 Arrangement Terminated true
Termination Date August 12, 2026
Aggregate Available 5,000
William Todd Horich [Member]  
Trading Arrangements, by Individual  
Name William Todd Horich
Title Senior Vice President, Chief Commercial Officer
Rule 10b5-1 Arrangement Terminated true
Termination Date August 12, 2026
Aggregate Available 44,000
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v3.26.3
Sage Acquisition - Schedule of Acquired Intangible Assets (Details) - Sage Acquisition - USD ($)
$ in Thousands
Dec. 31, 2025
Jul. 31, 2025
Business Combination [Line Items]    
Fair Value $ 142,900 $ 166,500
Estimated Useful Lives (in years)   8 years
Acquired developed technology and product rights    
Business Combination [Line Items]    
Fair Value $ 142,900  
Estimated Useful Lives (in years) 8 years  
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Contingent Consideration - Schedule of Current and Long-Term Contingent Consideration (Details) - USD ($)
$ in Thousands
Sep. 30, 2026
Dec. 31, 2025
Business Combination, Asset Acquisition, Transaction between Entities under Common Control, and Joint Venture Formation [Abstract]    
Contingent consideration, current portion $ 0 $ 31,052
Contingent consideration, long-term 206 206
Total $ 206 $ 31,258
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v3.26.3
Fair Value of Financial Instruments (Tables)
9 Months Ended
Sep. 30, 2026
Fair Value Disclosures [Abstract]  
Schedule of Fair Value of the Financial Assets and Liabilities
The Company's financial assets and liabilities that are required to be measured at fair value on a recurring basis are as follows (dollars in thousands):
Fair Value Measurements as of September 30, 2026 (unaudited)
Total
Level 1 Level 2Level 3
Assets:
Cash and cash equivalents
Cash$59,213 $59,213 $— $— 
Money market funds116,671 116,671 — — 
Marketable securities
Corporate debt securities183,575 — 183,575 — 
U.S government agency securities— —— —
Other noncurrent assets
Marketable securities - restricted (SERP)767 32 735 — 
Restricted cash
1,450 1,450 — — 
Total assets at fair value$361,676 $177,366 $184,310 $— 
Liabilities:
Contingent consideration$206 $— $— $206 
Total liabilities at fair value$206 $— $— $206 
Fair Value Measurements as of December 31, 2025
Total
Level 1 Level 2Level 3
Assets:
Cash and cash equivalents
Cash$56,371 $56,371 $— $— 
Money market funds72,077 72,077 — — 
Marketable securities
Corporate debt securities164,519 — 164,519 — 
Municipal debt securities14,716 —14,716 —
U.S. government agency debt securities987 —987 —
Other noncurrent assets
Marketable securities - restricted (SERP)705 27 678 — 
Restricted Cash1,450 1,450 — $— 
Total assets at fair value$310,825 $129,925 $180,900 $— 
Liabilities:
Contingent consideration$31,258 $— $— $31,258 
Total liabilities at fair value$31,258 $— $— $31,258 
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v3.26.3
Summary of Significant Accounting Policies
9 Months Ended
Sep. 30, 2026
Accounting Policies [Abstract]  
Summary of Significant Accounting Policies Summary of Significant Accounting Policies
Basis of Presentation
The Company's unaudited condensed consolidated financial statements have been prepared in accordance with the requirements of the U.S. Securities and Exchange Commission (SEC) for interim financial information. As permitted under Generally Accepted Accounting Principles in the United States (U.S. GAAP), certain notes and other information have been omitted from the interim unaudited condensed consolidated financial statements presented in this Quarterly Report on Form 10-Q. Therefore, these unaudited condensed consolidated financial statements should be read in conjunction with the Company's most recent Annual Report on Form 10-K, for the year ended December 31, 2025, filed with the SEC.
In management's opinion, the unaudited condensed consolidated financial statements include all normal and recurring adjustments necessary for a fair presentation of the Company's financial position, results of operations, and cash flows. The results of operations for any interim period are not necessarily indicative of the Company's future quarterly or annual results.
The Company, which is primarily located in the U.S., operates in one operating segment.
Reclassifications
The prior year amounts related to the caption Noncash lease expense have been reclassified from the caption Other noncash adjustments, net in the condensed consolidated statements of cash flows to conform to current year presentation. The reclassifications did not affect the other condensed consolidated financial statements.
Consolidation
The Company's unaudited condensed consolidated financial statements include the accounts of Supernus Pharmaceuticals, Inc. and its wholly owned subsidiaries. These are collectively referred to herein as "Supernus" or "the Company." Supernus Pharmaceuticals, Inc. and each of its subsidiaries are distinct legal entities. All material intercompany transactions and balances have been eliminated in consolidation.
The unaudited condensed consolidated financial statements reflect the consolidation of entities in which the Company has a controlling financial interest. In determining whether there is a controlling financial interest, the Company considers if it has a majority of the voting interests of the entity, or if the entity is a variable interest entity (VIE) and if the Company is the primary beneficiary. In determining the primary beneficiary of a VIE, the Company evaluates whether it has both: the power to direct the activities of the VIE that most significantly impact the VIE's economic performance; and the obligation to absorb losses of, or the right to receive benefits from the VIE that could potentially be significant to that VIE. The Company's judgment with respect to its level of influence or control of an entity involves the consideration of various factors, including the form of an ownership interest; representation in the entity's governance; the size of the investment; estimates of future cash flows; the ability to participate in policymaking decisions; and the rights of the other investors to participate in the decision making process, including the right to liquidate the entity, if applicable.
If the Company is not the primary beneficiary of the VIE, and an ownership interest is maintained in the entity, the interest is accounted for under the equity or cost methods of accounting, as appropriate.
The Company continuously assesses whether it is the primary beneficiary of a VIE as changes to existing relationships or future transactions may affect its conclusions.
Use of Estimates
The Company bases its estimates on: historical experience; forecasts; information received from its service providers; information from other sources, including public and proprietary sources; and other assumptions that the Company believes are reasonable under the circumstances. Actual results could differ materially from the Company's estimates. The Company periodically evaluates the methodologies employed in making its estimates.
Revenue Recognition
The Company determines revenue recognition for its contractual arrangements with customers based on the following five steps in accordance with Accounting Standards Codification (ASC) Topic 606, Revenue from Contracts with Customers (ASC 606): (1) identify each contract with a customer; (2) identify the performance obligations in the contract; (3) determine the transaction price; (4) allocate the transaction price to the performance obligations in the contract; and (5) recognize revenue when (or as) the Company satisfies the relevant performance obligation. The Company only applies the five-step model to contracts when it is probable that the Company will collect the consideration it is entitled to in exchange for the goods or services it transfers to the customer. The Company recognizes revenue in an amount that reflects the consideration the Company expects to receive in exchange for those goods or services. The Company does not adjust revenue for any financing effects in transactions where the Company expects the period between the transfer of the goods or services and collection to be less than one year.
Collaborative Arrangements
The Company has a collaboration agreement with Biogen Inc. (Biogen) (Biogen Collaboration Agreement) for the co-commercialization of ZURZUVAE in the U.S. ZURZUVAE is approved for the treatment of PPD in the U.S. ZURZUVAE is not approved for the treatment of Major Depressive Disorder (MDD) in the U.S.
The Company also has a collaboration agreement with Shionogi & Co., Ltd. (Shionogi) (Shionogi Collaboration Agreement) whereby the Company is entitled to receive royalties and milestone payments upon achievement of certain milestones related to the sale of zuranolone for the treatment of MDD in Japan, Taiwan and South Korea (the Shionogi Territory).
At contract inception, the Company analyzes its collaboration arrangements to assess whether they are within the scope of Accounting Standards Codification Topic 808, Collaborative Arrangements (ASC 808) to determine whether such
arrangements involve joint operating activities performed by parties that are both active participants in the activities and exposed to significant risks and rewards dependent on the commercial success of such activities. This assessment is performed throughout the life of the arrangement based on changes in the responsibilities of all parties in the arrangement. For collaboration arrangements within the scope of ASC 808 that contain multiple elements, the Company first determines which elements of the collaboration are deemed to be within the scope of ASC 808 and those that are more reflective of a vendor-customer relationship and therefore within the scope of Accounting Standards Codification Topic 606, Revenue from Contract with Customers, (ASC 606). For elements of collaboration arrangements that are accounted for pursuant to ASC 808, an appropriate recognition method is determined and applied consistently, either by analogy to authoritative accounting literature or by applying a reasonable and rational policy election.
For those elements of the arrangement that are accounted for pursuant to ASC 606, the Company performs the five-step model under ASC 606 as noted above to determine the appropriate amount of revenue to be recognized as it fulfills its obligations under each of its agreements and presents the arrangement as Royalty, licensing and other revenue or Collaboration revenue (ZURZUVAE) in the condensed consolidated statements of earnings (loss).
For those elements of the arrangement that are accounted for pursuant to ASC 808, the Company evaluates the income statement classification for presentation of amounts due from or owed to other participants associated with multiple activities in a collaboration arrangement based on the nature of each separate activity. Payments or reimbursements that are the result of a collaborative relationship instead of a vendor-customer relationship are recorded as an increase to Collaboration revenue (ZURZUVAE), an increase to or reduction of Cost of revenues, Research and development expense, or Selling, general and administrative expense, depending on the nature of the activity.
The Company applies ASC 808 and ASC 606 to the following collaboration agreements:
•Biogen - The Company has a collaboration agreement with Biogen for the co-commercialization of ZURZUVAE in the U.S. Revenues from the Biogen Collaboration Agreement include the Company’s share of ZURZUVAE revenues as that element of the agreement is accounted for under ASC Topic 808. The Company reports as Collaboration revenue (ZURZUVAE) its share of ZURZUVAE revenues, which is 50% of total net revenue recorded by Biogen for ZURZUVAE in the U.S.
The Company also identified the following promises in the Biogen Collaboration Agreement that were evaluated under the scope of ASC 606: delivery of (i) a co-exclusive license for SAGE-217 products in the U.S.; (ii) an exclusive license for SAGE-217 products outside of the United States other than Japan, the Republic of Korea, and Taiwan (Biogen Territory); (iii) commercial manufacturing supply of active pharmaceutical ingredient (API) and bulk drug product for SAGE-217 products in the Biogen Territory, and (iv) commercial manufacturing supply of API and bulk drug product for SAGE-217 in the U.S.
The Company also evaluated whether certain options outlined within the Biogen Collaboration Agreement represented material rights that would give rise to a performance obligation and concluded that none of the options convey a material right to Biogen and therefore are not considered separate performance obligations within the Biogen Collaboration Agreement.
The Company assessed the above promises at contract inception and determined that the co-exclusive license for SAGE-217 products in the U.S. is reflective of a vendor-customer relationship and therefore represent performance obligations within the scope of ASC 606. The co-exclusive license for SAGE-217 products in the U.S. is considered functional intellectual property and distinct from other promises under the contract. The exclusive license for SAGE-217 products in the Biogen Territory is considered a functional license that is distinct in the context of the Biogen Collaboration Agreement as Biogen can benefit from the license on its own or together with other readily available resources. As the co-exclusive license in the U.S. and the exclusive license in the Biogen Territory are delivered at the same time, they are considered one performance obligation at contract inception. The commercial manufacturing supply of API and bulk drug product for SAGE-217 products for the Biogen Territory, as well as in the U.S., are considered distinct in the context of the Biogen Collaboration Agreement as Biogen can benefit from the manufacturing services together with the licenses transferred by the Company at the inception of the Biogen Collaboration Agreement. Therefore, each represents a separate performance obligation within a contract with a customer under the scope of ASC 606 at contract inception. Accordingly, the transactions are recorded in Royalty, licensing, and other revenues.
•Shionogi - The Company also has a collaboration agreement with Shionogi whereby the Company is entitled to receive royalties and milestone payments upon achievement of certain milestones. The Shionogi Collaboration Agreement also includes arrangement for the supply of drug product for Shionogi’s clinical trials. The Company concluded that Shionogi meets the definition of a customer because the Company is delivering intellectual property and know-how rights for the
zuranolone program in support of territories in which the parties are not jointly sharing the risks and rewards. In addition, the Company determined that the Shionogi Collaboration Agreement met the requirements to be accounted for as a contract, including that it is probable that the Company will collect the consideration to which the Company is entitled in exchange for the goods or services that will be delivered to Shionogi. The Company assessed the promises at contract inception and determined that the license to zuranolone and supply of products to Shionogi are reflective of a vendor-customer relationship and therefore represent performance obligations within the scope of ASC 606.
The Company determined that the performance obligations in the Shionogi Collaboration Agreement included the license to zuranolone and the supply of certain materials during the clinical development phase, which includes the supply of API. The performance obligation related to the license to zuranolone was determined to be distinct from other performance obligations and therefore was a separate performance obligation for which control was transferred upon signing, and is recorded in Royalty, licensing, and other revenues. The obligation to provide certain clinical materials, including API for use during the development period, was determined to be a separate performance obligation, and is recorded in Royalty, licensing, and other revenues.
For additional information on the collaboration agreements with Biogen and Shionogi, as well as the Company's other collaboration arrangements, refer to Note 15, Collaboration Agreements.
Advertising Expense
Advertising expense includes the cost of promotional materials and activities, such as printed materials and digital marketing, marketing programs and speaker programs. The cost of the Company's advertising efforts is expensed as incurred.
In addition, under the collaboration agreement with Biogen, the Company and Biogen equally share in the costs of development and commercialization of ZURZUVAE. Commercial activities under the collaboration agreement may include advertising expenses. The Company's proportionate share of the costs of commercial activities under the collaboration agreement is recorded as a component of Selling, general and administrative expenses in the unaudited condensed consolidated statement of earnings (loss). Refer to Note 15, Collaboration Agreements.
The Company incurred $27.5 million and $82.6 million in advertising expense for the three and nine months ended September 30, 2026 and $22.4 million and $73.9 million in advertising expense for the three and nine months ended September 30, 2025, respectively. These expenses are recorded as a component of Selling, general and administrative expenses in the unaudited condensed consolidated statement of earnings (loss).
Insurance Recoveries
The Company has several policies with third-party insurers that provide for the recovery of certain costs incurred by the Company. The Company records its rights to insurance recoveries as a receivable when the respective costs are reimbursable under applicable insurance policies, it is probable that such costs will be reimbursed, and reimbursement can be reasonably estimated. As such, the Company estimates the percentage of costs that will be reimbursed by the insurance provider to determine the proper amount to record for the insurance receivable.
Insurance recoveries recognized are recorded as a reduction to Selling, general and administrative expenses. The Company had $6.2 million and $10.0 million of insurance recoveries during the three and nine months ended September 30, 2026, respectively, and $0.8 million and $6.2 million of insurance recoveries during the three and nine months ended September 30, 2025, respectively. Insurance receivable was $4.7 million and $1.8 million as of September 30, 2026 and December 31, 2025, respectively.
Recently Issued Accounting Pronouncements
New Accounting Pronouncements Not Yet Adopted
ASU 2024-03, Disaggregation of Income Statement Expenses (Topic 220) - The new standard, issued in November 2024, requires additional disclosure in tabular format, about the nature of specific types of expense captions presented on the face of the income statement as well as disclosures about selling expenses. The new standard does not change the requirements for the presentation of expenses on the face of the income statement. The standard is effective with annual periods beginning after December 15, 2026. Early adoption and retrospective application are permitted. The Company plans to adopt the guidance for the fiscal year ending December 31, 2027. We expect ASU 2024-03 to require additional disclosures in the notes to our consolidated financial statements. The Company is currently evaluating the effects the adoption of this guidance will have on the consolidated financial statements.
ASU 2025-06, Intangibles-Goodwill and Other-Internal-Use Software (Subtopic 350-40): Targeted Improvements to the Accounting for Internal-Use Software (ASU 2025-06) - The new standard, issued in September 2025, modernizes the accounting for internal-use software. ASU 2025-06 removes all references to software development stages and requires capitalization of software costs when management has committed to the software project and it is probable the software will be completed and perform its intended use. The Company plans to adopt the guidance for the fiscal year ending December 31, 2028. The Company is currently evaluating the timing and method of its adoption of ASU 2025-06 and the effects the adoption of this guidance will have on the consolidated financial statements.
ASU 2025-11, Interim Reporting - Narrow-Scope Improvements (Topic 270) - The new standard, issued in December 2025, clarifies the interim reporting requirements by improving navigability of Topic 270 and more clearly specifies what disclosures are required in an interim reporting period. It is not intended to significantly change interim reporting or expand or reduce interim disclosure requirements. The standard is effective for interim reporting periods in fiscal years beginning after December 15, 2027. Early adoption is permitted. The Company plans to adopt the guidance for the fiscal year ending December 31, 2028. The Company is currently evaluating the effects the adoption of this guidance will have on the consolidated financial statements.
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Summary of Significant Accounting Policies - Advertising Expense (Details) - USD ($)
$ in Millions
3 Months Ended 9 Months Ended
Sep. 30, 2026
Sep. 30, 2025
Sep. 30, 2026
Sep. 30, 2025
Accounting Policies [Abstract]        
Advertising costs $ 27.5 $ 22.4 $ 82.6 $ 73.9
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v3.26.3
Debt
9 Months Ended
Sep. 30, 2026
Debt Disclosure [Abstract]  
Debt Debt
Uncommitted Demand Secured Line of Credit
On February 8, 2023, the Company entered into a credit line agreement with UBS (the Credit Line). The Credit Line provides for a revolving line of credit of up to $150 million, which can be drawn at any time. Any fixed rate borrowing will bear interest at a fixed interest rate, equal to the sum of (i) the UBS Fixed Funding Rate (as defined in the Credit Line) plus (ii) the applicable Percentage Spread established in the Credit Line. Any variable rate borrowing will bear interest at a variable interest rate, equal to the sum of (i) the UBS Variable Rate (as defined in the Credit Line) plus (ii) the applicable Percentage Spread established in the Credit Line.
The Credit Line is secured by a first priority lien and security interest in certain of the Company's assets, including each account of the Company at UBS Financial Services Inc. (the Collateral Account), and other such collateral (collectively, the Collateral), as further defined in the Credit Line. The Company may be required to post additional collateral if the value of the Collateral declines below the required collateral maintenance requirements.
Upon certain customary events of default, all amounts due under the Credit Line will become immediately due and payable without demand, and UBS has the right, in its discretion, to liquidate, transfer, withdraw or sell all or any part of the Collateral and apply the proceeds to repay any borrowings pursuant to the Credit Line.
The Company has the right to repay any variable rate advance under the Credit Line at any time, in whole or in part, without penalty. The Company may repay any fixed rate advance in whole, but may not repay any fixed rate advance in part. In its discretion and without cause, UBS has the right at any time to demand full or partial payment of amounts borrowed pursuant to the Credit Line and terminate the Credit Line.
As of September 30, 2026 and December 31, 2025, there was no outstanding debt under the Credit Line.
In October 2026, the Company terminated the Credit Line.
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Summary of Significant Accounting Policies - Insurance Recoveries (Details) - USD ($)
$ in Millions
3 Months Ended 9 Months Ended
Sep. 30, 2026
Sep. 30, 2025
Sep. 30, 2026
Sep. 30, 2025
Dec. 31, 2025
Accounting Policies [Abstract]          
Insurance recoveries $ 6.2 $ 0.8 $ 10.0 $ 6.2  
Insurance settlements receivable, current $ 4.7   $ 4.7   $ 1.8
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v3.26.3
Investments - Schedule of Unrestricted Marketable Securities (Details) - USD ($)
$ in Thousands
Sep. 30, 2026
Dec. 31, 2025
Investments, Debt and Equity Securities [Abstract]    
Amortized cost $ 183,862 $ 180,215
Gross unrealized gains 0 34
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Condensed Consolidated Statements of Cash Flows - USD ($)
$ in Thousands
9 Months Ended
Sep. 30, 2026
Sep. 30, 2025
Cash flows from operating activities    
Net loss $ (39,751) $ (34,445)
Adjustments to reconcile net earnings (loss) to net cash provided by operating activities:    
Depreciation and amortization 75,506 66,547
Impairment charges 56,460 0
Amortization of premium/discount on marketable securities (41) (2,027)
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Share-based compensation expense 26,053 23,400
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Noncash lease expense 6,681 5,645
Inventory valuation write-down 10,183 1,228
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Accounts receivable (26,912) (5,885)
Inventories (10,945) (3,322)
Prepaid expenses and other assets 15,490 (6,274)
Accrued product returns and rebates 4,251 15,754
Accounts payable and other liabilities (7,528) (24,075)
Net cash provided by operating activities 68,320 27,470
Cash flows from investing activities    
Purchases of marketable securities (198,438) (385,741)
Maturities of marketable securities 194,832 735,161
Acquisition of Sage, net of cash acquired 0 (293,093)
Purchases of property and equipment (798) (911)
Net cash provided by (used in) investing activities (4,404) 55,416
Cash flows from financing activities    
Proceeds from issuance of common stock 20,128 29,059
Employee taxes paid related to net share settlement of equity awards (5,430) (4,198)
Payment of contingent consideration (31,178) (24,257)
Net cash provided by (used in) financing activities (16,480) 604
Net change in cash, cash equivalents, and restricted cash 47,436 83,490
Cash, cash equivalents, and restricted cash at beginning of period 129,898 69,331
Cash, cash equivalents, and restricted cash at end of period 177,334 152,821
Reconciliation of cash, cash equivalents, and restricted cash reported in the condensed consolidated balance sheets    
Cash and cash equivalents 175,884 151,371
Restricted cash 1,450 1,450
Total cash, cash equivalents, and restricted cash shown in the statement of cash flows 177,334 152,821
Supplemental cash flow information    
Cash paid for income taxes $ 1,641 $ 15,780
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Contingent Consideration - Schedule of Reconciliation of the Beginning and Ending Balances Related to the Contingent Consideration (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2026
Sep. 30, 2025
Sep. 30, 2026
Sep. 30, 2025
Fair Value, Net Derivative Asset (Liability) Measured on Recurring Basis, Unobservable Input Reconciliation [Roll Forward]        
Balance at beginning of period     $ 31,258 $ 47,340
Contingent consideration from Sage Acquisition       11,448
Change in fair value recognized in earnings     $ 2,391 $ 7,660
Change in fair value recognized in earnings, location     Contingent consideration loss Contingent consideration loss
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Reclassification to Other current liabilities       (27,705)
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$ in Thousands
Sep. 30, 2026
Dec. 31, 2025
Sep. 30, 2025
Other noncurrent assets      
Marketable securities - restricted (SERP) $ 767 $ 705  
Restricted cash 1,450 1,450 $ 1,450
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Liabilities:      
Contingent consideration 206 31,258  
Total liabilities at fair value 206 31,258  
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Marketable securities      
Marketable securities 183,575 164,519  
Municipal debt securities      
Marketable securities      
Marketable securities   14,716  
U.S government agency securities      
Marketable securities      
Marketable securities 0 987  
Cash      
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Money market funds      
Assets:      
Cash and cash equivalents 116,671 72,077  
Level 1      
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Marketable securities - restricted (SERP) 32 27  
Restricted cash 1,450 1,450  
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Total liabilities at fair value 0 0  
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Marketable securities   0  
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Marketable securities      
Marketable securities 0 0  
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Level 1 | Money market funds      
Assets:      
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Level 2      
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Restricted cash 0 0  
Total assets at fair value 184,310 180,900  
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Total liabilities at fair value 0 0  
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Marketable securities      
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Level 2 | Municipal debt securities      
Marketable securities      
Marketable securities   14,716  
Level 2 | U.S government agency securities      
Marketable securities      
Marketable securities 0 987  
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Share-Based Payments -Schedule of Performance Stock Units (Details) - Performance Shares [Member]
9 Months Ended
Sep. 30, 2026
$ / shares
shares
Number of PSUs  
Nonvested, beginning balance (in shares) | shares 390,496
Granted (in shares) | shares 236,466
Vested (in shares) | shares (103,989)
Forfeited (in shares) | shares (57,590)
Nonvested, ending balance (in shares) | shares 465,383
Weighted Average Grant Date Fair Value per Share  
Nonvested, beginning balance (in dollars per share) | $ / shares $ 30.80
Granted (in dollars per share) | $ / shares 47.73
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Forfeited (in dollars per share) | $ / shares 28.33
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$ in Thousands
Sep. 30, 2026
Dec. 31, 2025
Organization, Consolidation and Presentation of Financial Statements [Abstract]    
Raw materials $ 29,120 $ 31,833
Work in process 24,843 29,436
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v3.26.3
Goodwill and Intangible Assets, Net
9 Months Ended
Sep. 30, 2026
Intangible Asset, Goodwill and Other [Abstract]  
Goodwill and Intangible Assets, Net Goodwill and Intangible Assets, Net
Goodwill
The following table sets forth the gross carrying amounts of goodwill (dollars in thousands)
September 30,
2026
December 31,
2025
(unaudited)
Beginning balance$124,882 $117,019 
Goodwill activity from Sage Acquisition (a)
(5,451)7,863 
Ending balance
$119,431 $124,882 
(a) Refer to Note 3, Sage Acquisition for further detail.
Intangible Assets, Net
The following table sets forth the gross carrying amounts and related accumulated amortization of intangible assets subject to amortization (dollars in thousands):
September 30, 2026December 31, 2025
(unaudited)
Remaining Weighted
Average Life (Years)
Carrying Amount, GrossAccumulated AmortizationCarrying Amount, NetCarrying Amount, GrossAccumulated AmortizationCarrying Amount, Net
Acquired developed technology and product rights5.7$873,291 $(427,053)$446,238 $922,311 $(352,855)$569,456 
Amortization expense for intangible assets was $23.2 million and $74.2 million for the three and nine months ended September 30, 2026, respectively, and $24.3 million and $64.9 million for the three and nine months ended September 30, 2025, respectively.
In February 2025, the FDA approved ONAPGO and as such, the research and development efforts for the Company's acquired in-process research and development asset is considered complete. As of the FDA approval date, the ONAPGO intangible asset is a definite-life intangible asset subject to amortization and has a useful life of 10 years.
In July 2025, the Company acquired ZURZUVAE® (zuranolone), the first and only FDA-approved oral medicine indicated for the treatment of PPD in adults. The ZURZUVAE intangible asset is a definite-lived intangible asset subject to amortization and has a useful life of 8 years.
U.S. patents covering Trokendi XR and Oxtellar XR will expire no earlier than 2027. The Company entered into settlement agreements that allowed third parties to enter the Trokendi XR market on January 1, 2023. The Company entered into settlement and license agreements that allowed a third party to enter the Oxtellar XR market in September 2024.
The Company entered into settlement and license agreements that allows third parties to enter the XADAGO market in December 2027, or sooner under certain conditions.
The Company has entered into settlement agreements with third parties permitting the sale of a generic version of GOCOVRI beginning in June 2029, or sooner under certain conditions.
In the second quarter of 2026, the Company recognized impairment charges of $54.9 million related to its acquired intangible asset, APOKYN. The primary factors that led to the impairment determination were the performance of the commercial product and the change in the Company's future outlook of the brand as part of the Company's long-term planning process. The Company recognized as impairment loss the difference between the estimated fair value and carrying value of the intangible asset. The Company used the discounted cash flow income approach to estimate the fair values of the intangible assets. The primary inputs and assumptions used in the model included timing and projections of estimated future revenues and cash flows, and discount rate. The fair value measurement is classified as Level 3 within the fair value hierarchy as defined in ASC 820, Fair Value Measurement, due to the unobservable inputs used. The impairment loss is reported as Impairment charges in the condensed consolidated statements of earnings (loss).
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v3.26.3
Sage Acquisition (Tables)
9 Months Ended
Sep. 30, 2026
Business Combination, Asset Acquisition, Transaction between Entities under Common Control, and Joint Venture Formation [Abstract]  
Schedule of Purchase Price Allocation
The following purchase price allocation table presents the Company's estimates of the fair value of assets acquired and liabilities assumed as of the Sage Closing Date and subsequent measurement period adjustments recorded (unaudited, dollars in thousands):
As Initially Reported (a)
Measurement Period Adjustments (b)
As Adjusted
Cash and cash equivalents$243,197 $— $243,197 
Marketable securities
93,181 — 93,181 
Accounts receivable, net23,291 — 23,291 
Inventories, net (c)
50,714 1,897 52,611 
Prepaid expenses and other current assets (c)
18,674 (2,094)16,580 
Restricted cash
1,450 — 1,450 
Operating lease asset (d)
5,630 (520)5,110 
Intangible assets (e)
166,500 (23,600)142,900 
Deferred income tax assets, net (f)
— 47,935 47,935 
Other assets1,102 — 1,102 
Total fair value of assets acquired603,739 23,618 627,357 
Accounts payable and accrued liabilities 44,232 — 44,232 
Other liabilities (g)
— 23,969 23,969 
Operating lease liability12,380 — 12,380 
Total fair value of liabilities assumed56,612 23,969 80,581 
Total identifiable net assets547,127 (351)546,776 
Goodwill2,061 351 2,412 
Total purchase price$549,188 $— $549,188 
Cash consideration paid for Sage's common stock
$533,667 $— $533,667 
Cash consideration paid for cash settlement of Sage's equity awards
4,073 — 4,073 
Fair value of contingent consideration
11,448 — 11,448 
Total purchase price
$549,188 $— $549,188 
______________________________
(a) Amounts were initially reported within the Company's Quarterly Report on Form 10-Q for the quarter ended September 30, 2025, filed with the SEC on November 6, 2025.
(b) Measurement period adjustments reflect changes based on information related to the facts and circumstances that existed as of the acquisition date.
(c) Measurement period adjustment related to the refinement of the acquired inventory population.
(d) Refinement of the estimate of fair value of the right of use (ROU) asset associated with the acquired Sage headquarters lease. Refer to Note 13, Leases
(e) Measurement period adjustments to intangible assets are primarily due to update in inputs and assumptions based on information related to the facts and circumstances that existed as of the acquisition date.
(f) Represents the income tax impact of the transaction.
(g) Measurement period adjustment related to the Company's accounting policy related to the collaboration arrangement with Biogen.
Schedule of Acquired Intangible Assets
The following table summarizes the purchase price allocation, and the average remaining useful lives for identifiable intangible assets (unaudited, dollars in thousands):
Fair Value
Estimated Useful Lives
(in years)
Acquired developed technology and product rights$142,900 8
Total intangible assets$142,900 
Schedule of Pro Forma Information
The following table presents the unaudited pro forma combined financial information for each of the periods presented as if the Sage Acquisition had occurred on January 1, 2024 (dollars in thousands):
Three Months Ended September 30, 2025Nine Months Ended
September 30, 2025
(unaudited)(unaudited)
Pro forma total revenues
$199,637 $560,639 
Pro forma net loss
$(24,386)$(140,531)
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v3.26.3
Sage Acquisition - Narrative (Details)
$ / shares in Units, $ in Thousands
3 Months Ended 9 Months Ended
Jul. 31, 2025
USD ($)
right
$ / shares
Sep. 30, 2026
USD ($)
$ / shares
Sep. 30, 2025
USD ($)
Sep. 30, 2026
USD ($)
$ / shares
Sep. 30, 2025
USD ($)
Aug. 01, 2026
$ / shares
Dec. 31, 2025
$ / shares
Business Combination [Line Items]              
Common stock, par value (in dollars per share) | $ / shares   $ 0.001   $ 0.001   $ 0.001 $ 0.001
Amortization of intangible assets   $ 23,221 $ 24,325 $ 74,198 $ 64,930    
Sage Acquisition              
Business Combination [Line Items]              
Common stock, par value (in dollars per share) | $ / shares $ 0.0001            
Sage Acquisition              
Business Combination [Line Items]              
Business combination, price per share (in dollars per share) | $ / shares $ 8.50            
Aggregate consideration paid $ 561,000            
Contingents value rights | right 1            
Additional cash payments upon milestone achievements maximum $ 234,000 201,000   201,000      
Rights per share (in dollars per share) | $ / shares $ 3.50            
Contingent consideration, minimum   $ 0   0      
Amortization of intangible assets       $ 300      
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v3.26.3
Collaboration Agreements - Schedule of Revenue, Cost of Revenues, and Expense (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2026
Sep. 30, 2025
Sep. 30, 2026
Sep. 30, 2025
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
Selling, general and administrative $ 128,056 $ 179,678 $ 386,866 $ 363,173
Biogen Collaboration Agreement        
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
Collaboration revenue (ZURZUVAE) 41,697 20,164 104,690 20,164
Cost of revenues 641 434 2,967 434
Research and development expenses 504 (928) 1,797 (928)
Selling, general and administrative $ 27,998 $ 13,561 $ 77,907 $ 13,561
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Goodwill and Intangible Assets, Net - Schedule of Intangible Assets, Net (Details) - Acquired developed technology and product rights - USD ($)
$ in Thousands
Sep. 30, 2026
Dec. 31, 2025
Intangible Asset, Finite-Lived [Line Items]    
Remaining Weighted Average Life (Years) 5 years 8 months 12 days  
Carrying Amount, Gross $ 873,291 $ 922,311
Accumulated Amortization (427,053) (352,855)
Carrying Amount, Net $ 446,238 $ 569,456
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Share-Based Payments - Schedule of Share-based Compensation Expense (Details) - USD ($)
$ in Thousands
1 Months Ended 3 Months Ended 9 Months Ended
Jul. 31, 2025
Sep. 30, 2026
Sep. 30, 2025
Sep. 30, 2026
Sep. 30, 2025
Share-based payments          
Share-based compensation expense   $ 8,933 $ 30,745 $ 26,053 $ 46,320
Sage Acquisition          
Share-based payments          
Share-based compensation expense $ 22,900        
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Share-based payments          
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Investments (Tables)
9 Months Ended
Sep. 30, 2026
Investments, Debt and Equity Securities [Abstract]  
Schedule of Unrestricted Marketable Securities
Unrestricted available-for-sale marketable securities held by the Company are as follows (dollars in thousands):
September 30, 2026December 31, 2025
(unaudited)
Corporate, U.S. government agency and municipal debt securities
Amortized cost$183,862 $180,215 
Gross unrealized gains— 34 
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Investments
9 Months Ended
Sep. 30, 2026
Investments, Debt and Equity Securities [Abstract]  
Investments Investments
Marketable Securities
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September 30, 2026December 31, 2025
(unaudited)
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As of September 30, 2026, all of the Company's unrestricted available-for-sale marketable securities have contractual maturities of one year or less.
As of September 30, 2026 and December 31, 2025, there was no impairment due to credit loss on any available-for-sale marketable securities.
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v3.26.3
Sage Acquisition
9 Months Ended
Sep. 30, 2026
Business Combination, Asset Acquisition, Transaction between Entities under Common Control, and Joint Venture Formation [Abstract]  
Sage Acquisition Sage Acquisition
On July 31, 2025 (the Sage Closing Date), the Company completed its acquisition of all the outstanding equity of Sage Therapeutics, Inc. (Sage) pursuant to the Sage Merger Agreement dated June 13, 2025 (the Sage Acquisition). Under the terms of the Sage Merger Agreement, the Company commenced a tender offer to acquire all outstanding shares of Sage, par value $0.0001 per share (the Shares and each, a Share), at an offer price of (i) $8.50 per share in cash, less any applicable withholding taxes and without interest (the Cash Amount; an aggregate of approximately $561 million), plus (ii) one contingent value right per Share (the "CVR"; an aggregate of approximately $234 million, subject to the achievement of specific contingencies), which represents the right to receive up to $3.50, which is governed by the terms of a contingent value rights agreement entered into between the Company and CVR Agent (the Sage CVR Agreement), in cash, less any applicable withholding taxes and without interest. The transaction provides Supernus with the right to develop and market ZURZUVAE® (zuranolone) capsules, the first and only U.S. Food and Drug Administration (FDA)-approved oral medicine indicated for the treatment of adults with postpartum depression and a late-stage product candidate.

At the acquisition date, contingent payments of up to $234 million are due to the sellers upon the achievement of certain milestones related to the development and commercial sale of ZURZUVAE. The possible outcomes for the contingent consideration at the acquisition date range from $0 to $234 million on an undiscounted basis as of the Sage Closing Date. See Note 7, Contingent Consideration, for further discussion.

The acquisition was accounted for as a business combination under the acquisition method of accounting, in accordance with ASC 805, Business Combinations. The excess of the purchase price over the fair value of the net assets acquired was recorded as goodwill. The estimated fair values of the assets acquired and liabilities assumed, including goodwill, have been included in the Company's condensed consolidated financial statements since the Sage Closing Date.

In the third quarter of 2026, and within one year of the Sage Closing Date, the Company finalized its accounting for the business combination. During the measurement period, if the Company obtained new information regarding facts and circumstances that existed as of the Sage Closing Date that, if known, would have resulted in revised estimated values of those assets or liabilities, the Company accordingly revised its estimates of fair values and purchase price allocation. The effect of measurement period adjustments on the estimated fair value elements was reflected as if the adjustments had been made as of the Sage Closing Date. The impact of all changes that do not qualify as measurement period adjustments were included in current period earnings.

The following purchase price allocation table presents the Company's estimates of the fair value of assets acquired and liabilities assumed as of the Sage Closing Date and subsequent measurement period adjustments recorded (unaudited, dollars in thousands):
As Initially Reported (a)
Measurement Period Adjustments (b)
As Adjusted
Cash and cash equivalents$243,197 $— $243,197 
Marketable securities
93,181 — 93,181 
Accounts receivable, net23,291 — 23,291 
Inventories, net (c)
50,714 1,897 52,611 
Prepaid expenses and other current assets (c)
18,674 (2,094)16,580 
Restricted cash
1,450 — 1,450 
Operating lease asset (d)
5,630 (520)5,110 
Intangible assets (e)
166,500 (23,600)142,900 
Deferred income tax assets, net (f)
— 47,935 47,935 
Other assets1,102 — 1,102 
Total fair value of assets acquired603,739 23,618 627,357 
Accounts payable and accrued liabilities 44,232 — 44,232 
Other liabilities (g)
— 23,969 23,969 
Operating lease liability12,380 — 12,380 
Total fair value of liabilities assumed56,612 23,969 80,581 
Total identifiable net assets547,127 (351)546,776 
Goodwill2,061 351 2,412 
Total purchase price$549,188 $— $549,188 
Cash consideration paid for Sage's common stock
$533,667 $— $533,667 
Cash consideration paid for cash settlement of Sage's equity awards
4,073 — 4,073 
Fair value of contingent consideration
11,448 — 11,448 
Total purchase price
$549,188 $— $549,188 
______________________________
(a) Amounts were initially reported within the Company's Quarterly Report on Form 10-Q for the quarter ended September 30, 2025, filed with the SEC on November 6, 2025.
(b) Measurement period adjustments reflect changes based on information related to the facts and circumstances that existed as of the acquisition date.
(c) Measurement period adjustment related to the refinement of the acquired inventory population.
(d) Refinement of the estimate of fair value of the right of use (ROU) asset associated with the acquired Sage headquarters lease. Refer to Note 13, Leases
(e) Measurement period adjustments to intangible assets are primarily due to update in inputs and assumptions based on information related to the facts and circumstances that existed as of the acquisition date.
(f) Represents the income tax impact of the transaction.
(g) Measurement period adjustment related to the Company's accounting policy related to the collaboration arrangement with Biogen.

Acquired Inventory
The fair value of the inventory was estimated using the comparative sales method, which estimated the expected selling price of the product, reduced by all costs expected to be incurred to complete or to dispose of the inventory, as well as a profit on the sale.
Acquired Lease
As part of the Sage Acquisition, the Company acquired a lease for commercial real estate. The Company recognized a right-of-use asset and operating lease liability at the acquisition date. The amounts recognized reflect the present value of remaining lease payments, discounted at the Company's incremental borrowing rate. The fair value of the lease ROU asset was measured at an amount equal to the lease liability and evaluated for favorable or unfavorable lease terms when compared with market terms. Refer to Note 13, Leases, for further discussion of the acquired lease asset and assumed lease liability.
Acquired Intangible Assets
The acquired intangible asset includes the acquired developed technology and product rights. The Company estimated the fair value of the acquired intangible asset as of the Sage Closing Date using the income approach. The fair value measurements of the acquired intangible asset was estimated based on significant unobservable inputs and therefore, represent a Level 3 fair value measurement. Some of the more significant inputs and assumptions used in the intangible assets valuation include: the estimated future cash flows from product sales, probability of achieving regulatory approval in certain territories, the timing and projection of costs and expenses, and discount rates.
The following table summarizes the purchase price allocation, and the average remaining useful lives for identifiable intangible assets (unaudited, dollars in thousands):
Fair Value
Estimated Useful Lives
(in years)
Acquired developed technology and product rights$142,900 8
Total intangible assets$142,900 
Acquired intangible assets are amortized over their estimated useful lives on a straight-line basis. The Company recognized $0.3 million of amortization expense in the nine months ended September 30, 2026 which would have been recognized in the year ended December 31, 2025 if the adjustment to provisional amounts were recognized as of the Sage Closing Date.
Goodwill
Goodwill was calculated as the excess of the consideration paid consequent to completing the acquisition, compared to the net assets recognized. Goodwill represents the future economic benefits from the other acquired assets, and which could not be individually identified and separately valued. Goodwill is primarily attributable to the additional acquired growth platforms and an expanded revenue base. Goodwill is not deductible for tax purposes.
Revenues and Net Earnings of Sage
The operations of Sage and its subsidiaries have been included in the Company's condensed consolidated statements of earnings (loss) for the period subsequent to the Sage Closing Date.
Pro Forma Information
The following table presents the unaudited pro forma combined financial information for each of the periods presented as if the Sage Acquisition had occurred on January 1, 2024 (dollars in thousands):
Three Months Ended September 30, 2025Nine Months Ended
September 30, 2025
(unaudited)(unaudited)
Pro forma total revenues
$199,637 $560,639 
Pro forma net loss
$(24,386)$(140,531)
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v3.26.3
Contingent Consideration - Narrative (Details)
$ / shares in Units, $ in Thousands
3 Months Ended 9 Months Ended
Jul. 31, 2025
USD ($)
right
$ / shares
Sep. 30, 2026
USD ($)
Sep. 30, 2025
USD ($)
Jun. 30, 2025
USD ($)
Sep. 30, 2026
USD ($)
Sep. 30, 2025
USD ($)
Dec. 31, 2025
USD ($)
Apr. 30, 2025
USD ($)
Feb. 28, 2025
USD ($)
Dec. 31, 2024
milestone
Business Combination [Line Items]                    
Contingent consideration   $ 206     $ 206   $ 31,258      
Change in fair value recognized in earnings         (2,391) $ (7,660)        
Payment of contingent consideration         31,178 24,257        
Contingent consideration loss   0 $ 0   2,391 7,660        
Sage Acquisition                    
Business Combination [Line Items]                    
Contingents value rights | right 1                  
Rights per share (in dollars per share) | $ / shares $ 3.50                  
Additional cash payments upon milestone achievements maximum $ 234,000 201,000     201,000          
Contingent consideration $ 11,448           $ 11,448      
Contingent consideration, minimum   0     0          
Change in fair value recognized in earnings         (2,391) 0        
Contingent consideration loss   0 0   2,400 0        
Sage Acquisition | CVR Agreement                    
Business Combination [Line Items]                    
Contingent consideration   33,400     33,400          
Sage Acquisition | CVR Agreement                    
Business Combination [Line Items]                    
Rights per share (in dollars per share) | $ / shares $ 3.50                  
Sage Acquisition | CVR Agreement | Annual Net Sales of ZURZUVAE 2027                    
Business Combination [Line Items]                    
Rights per share (in dollars per share) | $ / shares $ 1.00                  
Contingent consideration, threshold, annual net sales $ 250,000                  
Sage Acquisition | CVR Agreement | Annual Net Sales of ZURZUVAE 2028                    
Business Combination [Line Items]                    
Rights per share (in dollars per share) | $ / shares $ 1.00                  
Contingent consideration, threshold, annual net sales $ 300,000                  
Sage Acquisition | CVR Agreement | Annual Net Sales of ZURZUVAE 2030                    
Business Combination [Line Items]                    
Rights per share (in dollars per share) | $ / shares $ 1.00                  
Contingent consideration, threshold, annual net sales $ 375,000                  
Sage Acquisition | CVR Agreement | First Commercial Sale In Japan For ZURZUVAE                    
Business Combination [Line Items]                    
Rights per share (in dollars per share) | $ / shares $ 0.50                  
USWM Acquisition                    
Business Combination [Line Items]                    
Additional cash payments upon milestone achievements maximum                 $ 25,000  
Number of outstanding milestones | milestone                   2
Change in fair value recognized in earnings   0 $ 0   0 $ (7,660)        
USWM Acquisition | ONAPGO                    
Business Combination [Line Items]                    
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USWM Acquisition | Subsequent Commercial Product Launch                    
Business Combination [Line Items]                    
Additional cash payments upon milestone achievements maximum               $ 30,000    
Contingent consideration   29,100     29,100          
Payment of contingent consideration   25,100   $ 2,300            
Business combination, contingent consideration, liability insurance recoveries   $ 4,000     $ 4,000          
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v3.26.3
Business Organization
9 Months Ended
Sep. 30, 2026
Organization, Consolidation and Presentation of Financial Statements [Abstract]  
Business Organization Business Organization
Supernus Pharmaceuticals, Inc. (the Company, see Consolidation in Note 2, Summary of Significant Accounting Policies) is a biopharmaceutical company focused on developing and commercializing products for the treatment of central nervous system (CNS) diseases. The Company's diverse neuroscience portfolio includes approved treatments for attention-deficit hyperactivity disorder (ADHD), dyskinesia in Parkinson's Disease (PD) patients receiving levodopa-based therapy, hypomobility in PD, postpartum depression (PPD), epilepsy, migraine, cervical dystonia, and chronic sialorrhea. The Company is developing a broad range of novel product candidates for CNS disorders.
The Company has nine commercial products that it markets in the United States (U.S.): Qelbree®, GOCOVRI®, Oxtellar XR®, Trokendi XR®, APOKYN®, XADAGO®, MYOBLOC®, ONAPGOTM (formerly known as SPN-830), and ZURZUVAE® (acquired through the acquisition of Sage Therapeutics, Inc.). The Company does not directly market its products outside the U.S.
Merger of Equals with Indivior Pharmaceuticals, Inc.
On August 1, 2026, the Company entered into an Agreement and Plan Of Merger (the "Merger Agreement"), by and among the Company, Indivior Pharmaceuticals, Inc., a Delaware corporation (Indivior), and Artemis Merger Sub Inc., a Delaware corporation and a wholly-owned subsidiary of Indivior (Merger Sub).
Pursuant to the Merger Agreement, and upon the terms and subject to the conditions thereof, Merger Sub will merge with and into the Company (the "Merger"), with the Company continuing as the surviving corporation and a wholly-owned subsidiary of Indivior. Following the completion of the Merger, Indivior will be renamed "Supernus, Inc." and its shares of common stock are expected to continue trading on the Nasdaq Stock Market under the ticker symbol "SUPN". The Merger and the other transactions contemplated by the Merger Agreement are referred to collectively as the "Transactions". The consummation of the Transactions is subject to various regulatory approvals and customary terms and conditions set forth in the Merger Agreement.

At the effective time of the Merger (the "Effective Time"), each share of common stock, par value $0.001 per share, of the Company (each, a "Company Share") issued and outstanding immediately prior to the Effective Time (other than certain excluded shares) will be converted into the right to receive 1.5401 shares of common stock, par value $0.001 per share, of Indivior (each, an "Indivior Share" and, such ratio, the "Exchange Ratio," and the Indivior Shares issuable in the Merger, the "Merger Consideration"). Immediately prior to the Effective Time, stockholders of Indivior will receive a one-time special cash dividend of $1.0 billion. Indivior has secured a debt commitment of $650 million through a term loan facility, and the remaining portion will be funded by existing cash of the then-combined company. The Exchange Ratio is fixed and will not be adjusted for changes in the market price of either the Company Shares or the Indivior Shares.

Refer to Note 18, Subsequent Events for further details.
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v3.26.3
Condensed Consolidated Statements of Comprehensive Earnings (Loss) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2026
Sep. 30, 2025
Sep. 30, 2026
Sep. 30, 2025
Statement of Comprehensive Income [Abstract]        
Net earnings (loss) $ 20,913 $ (45,117) $ (39,751) $ (34,445)
Other comprehensive gain (loss)        
Unrealized gain (loss) on marketable securities, net of tax (142) 129 (236) 118
Other comprehensive gain (loss) (142) 129 (236) 118
Comprehensive earnings (loss) $ 20,771 $ (44,988) $ (39,987) $ (34,327)
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v3.26.3
Summary of Significant Accounting Policies - Revenue Recognition (Details)
9 Months Ended
Sep. 30, 2026
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Collaboration revenue, percentage 50.00%
Biogen | Clinical Supply Agreement  
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Income Tax Expense (Benefit) (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2026
Sep. 30, 2025
Sep. 30, 2026
Sep. 30, 2025
Dec. 31, 2025
Income Tax Disclosure [Abstract]          
Income tax expense (benefit) $ 1,796 $ (12,837) $ (1,138) $ (12,671)  
Effective tax rate 7.90% 22.20% 2.80% 26.90%  
Income tax receivable $ 24,900   $ 24,900   $ 38,400
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Income Tax Expense (Benefit) (Tables)
9 Months Ended
Sep. 30, 2026
Income Tax Disclosure [Abstract]  
Schedule of Effective Income Tax Rate Reconciliation
The following table provides information regarding the Company's income tax expense (benefit) for the three and nine months ended September 30, 2026 and 2025 (dollars in thousands):
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)(unaudited)
Income tax expense (benefit)$1,796 $(12,837)$(1,138)$(12,671)
Effective tax rate7.9 %22.2 %2.8 %26.9 %
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Business Organization (Details)
$ / shares in Units, $ in Millions
9 Months Ended
Aug. 01, 2026
USD ($)
$ / shares
shares
Sep. 30, 2026
product
$ / shares
Dec. 31, 2025
$ / shares
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]      
Number of commercial products | product   9  
Common stock, par value (in dollars per share) | $ / shares $ 0.001 $ 0.001 $ 0.001
Invidior Pharmaceuticals, Inc. | Acquisition Term Loan | Unsecured Debt      
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]      
Commitments to extend credit $ 650    
Supernus Pharmaceuticals, Inc. | Invidior Pharmaceuticals, Inc.      
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]      
Business combination, share exchange ratio | shares 1.5401    
One-time special cash dividend $ 1,000    
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v3.26.3
Earnings (Loss) per Share (Tables)
9 Months Ended
Sep. 30, 2026
Earnings Per Share [Abstract]  
Schedule of Computation of Basic and Diluted Earnings Per Share
The following table sets forth the computation of basic and diluted earnings per share for the three and nine months ended September 30, 2026 and 2025 (dollars in thousands, except share and per share amounts):
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)(unaudited)
Numerator:
Net earnings (loss)$20,913 $(45,117)$(39,751)$(34,445)
Numerator for basic and dilutive earnings (loss) per share$20,913 $(45,117)$(39,751)$(34,445)
Denominator:
Weighted average shares outstanding, basic58,202,474 56,552,741 57,975,499 56,133,918 
Effect of dilutive securities:
Stock options and stock awards1,268,547 — — — 
Weighted average shares outstanding, diluted59,471,021 56,552,741 57,975,499 56,133,918 
Earnings (loss) per share, basic$0.36 $(0.80)$(0.69)$(0.61)
Earnings (loss) per share, diluted$0.35 $(0.80)$(0.69)$(0.61)
Schedule of Common Stock Equivalents Excluded in the Calculation of Diluted Earnings Per Share
The following table sets forth the common stock equivalents of outstanding stock-based awards excluded in the calculation of diluted earnings (loss) per share, because the vesting conditions have not been met as of the end of the reporting period or their inclusion would be anti-dilutive:
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)(unaudited)
Stock options and stock awards496,023 647,044 7,449,141 743,145 
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v3.26.3
Condensed Consolidated Statements of Earnings (Loss) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2026
Sep. 30, 2025
Sep. 30, 2026
Sep. 30, 2025
Revenues        
Total revenues $ 226,771 $ 192,103 $ 653,534 $ 507,380
Costs and expenses        
Cost of revenues [1] 27,018 18,965 84,078 51,555
Research and development 25,756 29,366 94,657 78,408
Selling, general and administrative 128,056 179,678 386,866 363,173
Amortization of intangible assets 23,221 24,325 74,198 64,930
Impairment charges 1,541 0 56,460 0
Contingent consideration loss 0 0 2,391 7,660
Total costs and expenses 205,592 252,334 698,650 565,726
Operating earnings (loss) 21,179 (60,231) (45,116) (58,346)
Other income (expense)        
Interest and other income, net 2,248 2,277 7,260 11,230
Interest expense (718) 0 (3,033) 0
Total other income, net 1,530 2,277 4,227 11,230
Earnings (loss) before income taxes 22,709 (57,954) (40,889) (47,116)
Income tax expense (benefit) 1,796 (12,837) (1,138) (12,671)
Net earnings (loss) $ 20,913 $ (45,117) $ (39,751) $ (34,445)
Earnings (loss) per share        
Basic (in dollars per share) $ 0.36 $ (0.80) $ (0.69) $ (0.61)
Diluted (in dollars per share) $ 0.35 $ (0.80) $ (0.69) $ (0.61)
Weighted average shares outstanding        
Basic (in shares) 58,202,474 56,552,741 57,975,499 56,133,918
Diluted (in shares) 59,471,021 56,552,741 57,975,499 56,133,918
Net product sales        
Revenues        
Total revenues $ 178,576 $ 168,542 $ 495,042 $ 468,525
Collaboration revenue (ZURZUVAE)        
Revenues        
Total revenues 41,697 20,164 104,690 20,164
Royalty, licensing, and other revenues        
Revenues        
Total revenues $ 6,498 $ 3,397 $ 53,802 $ 18,691
[1] Excludes amortization of intangible assets
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v3.26.3
Share-Based Payments - Schedule of Restricted Stock Units (Details) - RSUs
9 Months Ended
Sep. 30, 2026
$ / shares
shares
Number of RSUs  
Nonvested, beginning balance (in shares) | shares 396,693
Granted (in shares) | shares 122,609
Vested (in shares) | shares (165,678)
Forfeited (in shares) | shares (11,375)
Nonvested, ending balance (in shares) | shares 342,249
Weighted Average Grant Date Fair Value per Share  
Nonvested, beginning balance (in dollars per share) | $ / shares $ 32.98
Granted (in dollars per share) | $ / shares 50.20
Vested (in dollars per share) | $ / shares 33.43
Forfeited (in dollars per share) | $ / shares 37.89
Nonvested, ending balance (in dollars per share) | $ / shares $ 38.77
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v3.26.3
Commitments and Contingencies
9 Months Ended
Sep. 30, 2026
Commitments and Contingencies Disclosure [Abstract]  
Commitments and Contingencies Commitments and Contingencies
Product Licenses
The Company has obtained exclusive licenses from third parties for proprietary rights to support the product candidates in the Company's CNS portfolio. Under these license agreements, the Company may be required to pay certain amounts upon the achievement of defined milestones. If these products are ultimately commercialized, the Company is also obligated to pay royalties to third parties, computed as a percentage of net product sales, for each respective product under a license agreement.
Through the USWM Acquisition, the Company acquired licensing agreements with other pharmaceutical companies for APOKYN, ONAPGO, XADAGO, and MYOBLOC. The Company is obligated to pay royalties to third parties, computed as a percentage of net product sales, for each of the products under the respective license agreements. The royalty expense incurred for these acquired products is recognized as Cost of revenues in the condensed consolidated statements of earnings (loss).
Through the Sage Acquisition, the Company acquired licensing agreements with other pharmaceutical companies for ZURZUVAE (zuranolone). See Note 15, Collaboration Agreements for further details.
Navitor Development Agreement and Asset Purchase Agreement
In April 2020, the Company entered into a development agreement (Development Agreement) with Navitor Pharmaceuticals, Inc. (Navitor Inc.). The Company agreed to bear certain Phase I and Phase II development costs incurred by either party, up to a maximum of $50 million, which amount could be increased under the terms of the Development Agreement upon Navitor's request and the Company's consent. In 2020, the Company paid a one-time, nonrefundable, and non-creditable fee of $10 million for the option to acquire or license NV-5138 (SPN-820) (Purchase Option) and made a $15 million equity investment representing approximately 13% ownership in Navitor Inc. The Company acquired Series D Preferred Shares of Navitor Inc. (the Navitor Shares), an equity investment representing an approximately 13% ownership position in Navitor Inc. As part of a legal restructuring in March 2021, the Company's Navitor Shares were exchanged for membership interests in Navitor Pharmaceutics LLC (Navitor LLC), which became the sole shareholder of Navitor Inc. The Company determined that although Navitor LLC was a VIE, the Company did not consolidate the results of this VIE into its financial results because the Company lacked the power to direct the activities that most significantly impact Navitor's economic performance.
On April 1, 2026, the Company entered into an Asset Purchase Agreement (APA) with Navitor and consummated the transactions contemplated therein whereby the Company acquired, among other things, the right, title, materials, and intellectual property of SPN-820. The transaction included no upfront cash payment, however, the Company is obligated to effect and complete one Phase 2b study and make several milestone payments of up to $350 million contingent upon the achievement of specified development, regulatory and commercial milestones. The Company accounted for the transaction as an asset purchase under ASC 805 Business Combinations. The Company accounted for the contingent milestone payments under ASC 450 Contingencies. As such, no contingent liability was recognized as the contingent milestones were deemed not probable of achievement as of April 1, 2026 and September 30, 2026. The Company retains its 13% equity ownership in Navitor LLC. The Company determined Navitor LLC no longer meets the criteria to be considered a VIE. The Company continues to record its share of the results of Navitor LLC, a private company, on a quarter lag as the financial information of Navitor LLC is not available on a sufficiently timely basis for the Company to apply the equity method of accounting.
Other than as described herein, no additional equity investment has been made or financing has been provided to Navitor Inc. or Navitor LLC.
USWM Enterprise Commitments Assumed
As part of the USWM Acquisition, the Company assumed the remaining commitments of USWM Enterprises and its subsidiaries, which included an annual minimum purchase requirement of MYOBLOC under the contract manufacturing agreement with Merz for manufacture and supply. An amendment to the contract manufacturing agreement with Merz was executed in July 2025. Amendments to the contract manufacturing agreement included among other things, the removal of the annual minimum purchase requirement of MYOBLOC, and the Company's agreement to pay a nonrefundable annual fee of €3.0 million to cover general maintenance and reservation costs for the manufacturing facilities.
Biscayne Amendment
On January 22, 2026, the Company entered into a First Amendment (Amendment) to the Agreement and Plan of Merger (Agreement) dated September 12, 2018, with former Biscayne security holders. The Amendment relates to the timing and payment of certain milestones under the Biscayne merger agreement. The Company agreed to pay former Biscayne security holders $10.0 million, one of the milestones specified in the Agreement, by June 30, 2026. The Company subsequently paid the Biscayne security holders in June 2026. The amount is recorded in Research and development expense on the condensed consolidated statements of earnings (loss) for the nine months ended September 30, 2026.
Claims and Litigation
From time to time, any of Supernus Pharmaceuticals, Inc. or one or more of its subsidiaries may be involved in various claims, litigation, legal proceedings, and governmental and regulatory investigations. These matters may involve patent litigation, product liability, product-related litigation, securities law-related litigation, commercial and other matters, and government investigations, among others. On a quarterly basis, the Company reviews the status of each significant matter and assesses its potential financial exposure. If the potential loss from any claim, asserted or unasserted, or legal proceeding is considered probable and the amount can be reasonably estimated, the Company will accrue a liability for the estimated loss. Because of uncertainties related to claims, legal proceedings and litigation, accruals will be based on the Company's best estimates based on available information. The Company may reassess the potential liability related to these matters and may revise these estimates. The process of resolving matters through litigation or other means is inherently uncertain and it is possible that an unfavorable resolution of these matters will adversely affect the Company, its results of operations, financial condition and cash flows.
APOKYN Litigation
On October 3, 2022, Sage Chemical, Inc. and TruPharma, LLC filed a lawsuit in the United States District Court for the District of Delaware alleging that Supernus Pharmaceuticals, Inc., Britannia Pharmaceuticals Limited (Britannia), and US WorldMeds Partners, LLC (US WorldMeds) violated state and federal antitrust law in connection with APOKYN® (apomorphine HCl). On October 16, 2022, Plaintiffs amended their complaint to add additional defendants MDD US Enterprises, LLC, MDD US Operations, LLC (each a subsidiary of Supernus Pharmaceuticals, Inc.), USWM, LLC (USWM), and individual defendants Paul Breckinridge Jones, Sr., Herbert Lee Warren, Jr., Henry Van Den Berg, and Kristin L. Gullo. On January 10, 2023, Defendants filed an Omnibus Motion to Dismiss the Amended Complaint seeking dismissal of each of Plaintiffs’ claims and the lawsuit in its entirety and US WorldMeds with USWM, Britannia, and the group of individual defendants each filed separate motions to dismiss. On May 9, 2024, and May 28, 2024, respectively, the Court denied the Defendants’ omnibus motion and the Britannia motion to dismiss. On May 31, 2024, and June 4, 2024, respectively, the Court granted the individual defendants’ motion to dismiss and the US WorldMeds and USWM motion to dismiss. On December 6, 2024, Plaintiffs filed a second amended complaint, which added US WorldMeds and USWM back to the case. On February 9, 2026, the Court issued a scheduling order that provided for the close of expert discovery on May 8, 2026, and the submission of dispositive motions by June 9, 2026, with briefing to be completed on September 2, 2026. On June 9, 2026, each side submitted both dispositive motions and motions to exclude certain expert opinions, which are currently being briefed. The scheduling order also sets a pretrial conference on January 15, 2027, and a jury trial beginning on January 25, 2027.
The Company intends to defend itself vigorously. However, the Company can offer no assurances that it will be successful in a litigation.
Sage Legal Proceedings
Merger Complaints
In connection with the Sage Merger Agreement and Sage's Board of Directors' (Sage Board) recommendation to Sage shareholders to tender their shares pursuant to the tender offer, two purported Sage shareholders filed complaints in state court against Sage and each member of the Sage Board. Among other things, the complaints assert claims for negligent misrepresentation and concealment and negligence under New York common law. Sage has also received certain demand letters from other purported shareholders with similar allegations to those contained in the complaints. Additional demand letters may be received by Sage and additional complaints may be filed against Sage, the Sage Board, Supernus and Saphire, Inc. in connection with the Sage Merger Agreement and tender offer.
Securities Class Action
On August 28, 2024, named plaintiff Darren Korver filed a purported federal securities class action lawsuit in the Southern District of New York against Sage and individuals, Barry E. Greene and Kimi Iguchi (Securities Class Action). The complaint in the Securities Class Action alleges violations of U.S. securities laws under Sections 10(b) and 20(a) of the Securities Exchange Act of 1934 and Rule 10b-5 promulgated thereunder and seeks an as-yet unspecified amount of damages allegedly sustained by parties who purchased Sage stock between April 12, 2021 and July 23, 2024, as well as applicable attorneys’ fees and costs. On April 17, 2025, Sage Therapeutics, along with all of the individual defendants, filed a motion to dismiss the Securities Class Action in the Southern District of New York.
On February 18, 2026, Plaintiffs filed a letter with the Court seeking leave to amend their complaint and asking the Court to refrain from deciding the motion to dismiss pending the Court’s decision on the request to file an amended complaint. On March 10, 2026, Defendants submitted a letter to the Court joining Plaintiffs’ request of February 18, 2026. On April 3, 2026, the
parties filed a stipulation, which the Court so ordered on April 9, 2026, permitting Plaintiffs to file an amended complaint by July 15, 2026. On April 30, 2026, Plaintiffs filed the Second Amended Complaint. On July 15, 2026, Defendants filed a motion to dismiss the Second Amended Complaint. Plaintiffs’ opposition to the Motion to Dismiss was filed on August 31, 2026. Defendants’ reply in further support of their Motion to Dismiss was filed on September 22, 2026. The Parties are currently awaiting the Court’s ruling on the Motion to Dismiss briefing. Related derivative actions remain stayed pending the resolution of this motion.
Sage denies any allegations of wrongdoing and intends to vigorously defend against the Securities Class Action.
U.S. Securities and Exchange Commission (SEC) Investigation
On October 16, 2024, Sage Therapeutics received a subpoena from the Enforcement Division of the SEC requesting documents and information related to Sage’s NDA for zuranolone for the treatment of MDD, including communications with the FDA and any communications containing material nonpublic information. The Company is cooperating with the SEC and intends to continue to provide information responsive to the SEC’s requests.
Consolidated Derivative Litigations
On March 26, 2025, plaintiff shareholder Qingping Zhu commenced derivative litigation in the Southern District of New York, purportedly on behalf of Sage, against sixteen current and former officers and directors of Sage (the Zhu Derivative Litigation). Based significantly on the allegations underlying the Securities Class Action, the Zhu Derivative Litigation alleges violations of Section 14(a) of the Exchange Act and Rule 14a-9 promulgated thereunder, breaches of fiduciary duty, unjust enrichment, and waste of corporate assets, and seeks unspecified damages and various equitable relief. On April 14, 2025, the Southern District of New York granted a stay of the Zhu Derivative Litigation pending the resolution of the motion to dismiss the amended complaint in the Securities Class Action.
On May 13, 2025, plaintiff shareholder Jurgen Matton commenced derivative litigation in the Southern District of New York, purportedly on behalf of Sage Therapeutics, against sixteen current and former officers and directors of Sage Therapeutics (the Matton Derivative Litigation). Based significantly on the allegations underlying the Securities Class Action, the Matton Derivative Litigation alleges violations of Section 14(a) of the Exchange Act and Rule 14a-9 promulgated thereunder, breaches of fiduciary duty, unjust enrichment, and waste of corporate assets, and seeks unspecified damages and various equitable relief.

On May 22, 2025, plaintiff shareholder Joseph Pizzelanti commenced derivative litigation in the Southern District of New York, purportedly on behalf of Sage Therapeutics, against sixteen current and former officers and directors of the Company (the Pizzelanti Derivative Litigation). Based significantly on the allegations underlying the Securities Class Action, the Pizzelanti Derivative Litigation alleges violations of Section 14(a) of the Exchange Act and Rule 14a-9 promulgated thereunder, breaches of fiduciary duty, unjust enrichment, and waste of corporate assets, and seeks unspecified damages and various equitable relief.

On April 14, 2025, the Southern District of New York granted a stay of the Zhu Derivative Litigation pending the resolution of the motion to dismiss the amended complaint in the Securities Class Action. Subsequently, the Matton Derivative Litigation and Pizzelanti Derivative Litigation were consolidated with the Zhu Derivative Litigation ("Consolidated Derivative Litigation") and stayed along with the Zhu Derivative Litigation pending the resolution of Sage’s motion to dismiss in the Securities Class Action.
At this time, the Company is unable to predict the outcome of the Merger Complaints, Securities Class Action, the SEC investigation, or the Consolidated Derivative Litigation, or reasonably estimate a range of possible losses. The outcome of the matters described above cannot be predicted with certainty.
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v3.26.3
Subsequent Event
9 Months Ended
Sep. 30, 2026
Subsequent Events [Abstract]  
Subsequent Event Subsequent Events
Merger of Equals with Indivior Pharmaceuticals, Inc.
On October 15th, at the special meeting of the Company's stockholders, the Company's stockholders approved the Merger and related proposals. The definitive proxy statement pertaining to the special meeting was previously filed by the Company with the Securities and Exchange Commission on September 11, 2026. All proposals presented at the special meeting were approved by the Company’s stockholders, including (i) approval to adopt the Merger Agreement (ii) approval of certain compensation that will become payable in connection with the Merger, as well as certain compensation that may become payable to Supernus's named executive officers upon a termination in connection with the Merger.
The Merger is expected to be consummated on November 2, 2026 (the “Expected Closing Date”).
Additionally, on the Expected Closing Date, the Combined Company and certain of its subsidiaries (collectively, the “Loan Parties”) are expected to enter into a Credit Agreement (the “Credit Agreement”) by and among the Combined Company, as the borrower, the other Loan Parties, as guarantors, the financial institutions from time to time party thereto as lenders, and a financial institution, as agent for the lenders and for itself as lender, providing for a senior secured term loan facility (the “Credit Facility”) in an aggregate principal amount of $650 million, all of which is expected to be borrowed on the Expected Closing Date.
The proceeds of the Credit Facility are expected to be permitted to be used, in whole or in part, to consummate the Merger, repay existing indebtedness on the Expected Closing Date (including any outstanding indebtedness and obligations under that certain Credit Line Agreement, dated February 8, 2023, among the Company and UBS Bank USA), to pay costs and expenses in connection therewith and for general corporate purposes (including, without limitation, acquisitions and investments permitted under the Credit Agreement).
As previously disclosed by Indivior, its board of directors declared a special cash dividend (the “Special Dividend”) in the amount of (i) $8.13 per share of Indivior common stock payable to holders of record of the issued and outstanding Indivior common stock as of October 30, 2026 (the “Special Dividend Record Date”) (such holders, the “Special Dividend Record Holders”) and (ii) $8.13 per share of Indivior common stock underlying Indivior equity awards on the Special Dividend Record Date payable, upon vesting of such equity awards, to holders of certain Indivior equity awards outstanding as of the Special Dividend Record Date (the “Special Dividend Award Holders”). The payment of the Special Dividend is subject to and contingent upon the closing of the Merger (the “Closing”) and will be made following the Closing. Assuming the Merger is consummated on the Expected Closing Date, payment of the Special Dividend to Special Dividend Record Holders is anticipated to be made on or about November 6, 2026. Supernus stockholders will not be entitled to receive the Special Dividend with respect to any Indivior common stock received as consideration in the Merger.
ONAPGO
In October 2026, the FDA recognized seven years of orphan-drug exclusive approval for ONAPGO (apomorphine HCl) for the treatment of motor fluctuations in adults with advanced Parkinson’s disease. The seven-year market exclusivity for ONAPGO began on February 3, 2025, the date of FDA approval.
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v3.26.3
Condensed Consolidated Balance Sheets (Parenthetical) - $ / shares
Sep. 30, 2026
Dec. 31, 2025
Stockholders' equity    
Common stock, par value (in dollars per share) $ 0.001 $ 0.001
Common stock, authorized (in shares) 130,000,000 130,000,000
Common stock, issued (in shares) 58,254,131 57,457,462
Common stock, outstanding (in shares) 58,254,131 57,457,462
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v3.26.3
Commitments and Contingencies (Details)
$ in Thousands, € in Millions
1 Months Ended 9 Months Ended
May 22, 2025
defendant
May 13, 2025
defendant
Mar. 26, 2025
defendant
Jun. 30, 2026
USD ($)
Apr. 30, 2020
USD ($)
Sep. 30, 2026
USD ($)
plaintiff
Sep. 30, 2025
USD ($)
Sep. 30, 2026
EUR (€)
Apr. 01, 2026
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study
Long-term Purchase Commitment [Line Items]                  
Payment of contingent consideration       $ 10,000   $ 28,109 $ 4,900    
Merger Agreement | Sage Litigation                  
Long-term Purchase Commitment [Line Items]                  
Number of plaintiff | plaintiff           2      
Derivative Litigation | Sage Litigation                  
Long-term Purchase Commitment [Line Items]                  
Number of defendants | defendant 16 16 16            
USWM Acquisition                  
Long-term Purchase Commitment [Line Items]                  
Annual minimum purchase quantity requirement amount | €               € 3.0  
Navitor Pharmaceuticals, Inc.                  
Long-term Purchase Commitment [Line Items]                  
Threshold for development costs payments         $ 50,000        
Collaborative arrangement, payment for one time fee         10,000        
Collaborative arrangement, number of studies | study                 1
Collaborative arrangement, contingent consideration, maximum                 $ 350,000
Navitor Pharmaceuticals, Inc. | Variable Interest Entity, Not Primary Beneficiary                  
Long-term Purchase Commitment [Line Items]                  
Investments         $ 15,000        
VIE, qualitative or quantitative information, ownership percentage         13.00%        
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v3.26.3
Leases
9 Months Ended
Sep. 30, 2026
Leases [Abstract]  
Leases Leases
Operating lease assets and lease liabilities as reported on the condensed consolidated balance sheets are as follows (dollars in thousands):

Balance Sheet ClassificationSeptember 30, 2026December 31, 2025
(unaudited)
Assets
Operating lease assetsOther assets$23,059 $26,712 
Total lease assets$23,059 $26,712 
Liabilities
Operating lease liabilities, current portionAccounts payable and accrued liabilities$7,620 $10,612 
Operating lease liabilities, long-termOperating lease liabilities, long-term28,577 30,365 
Total lease liabilities$36,197 $40,977 

Supplemental cash flow information related to leases is as follows (dollars in thousands):
Nine Months Ended
September 30,
20262025
(unaudited)
Cash paid for operating leases$17,411 $14,415 
Lease assets obtained for new operating leases4,569 9,941 
Lease obtained from Sage Acquisition
As part of the Sage Acquisition, the Company acquired a lease for office space located in a multi-tenant building located in Cambridge, Massachusetts and classified this as an operating lease. Sage's office space lease term continues through February 28, 2030 unless terminated earlier in accordance with the terms of the lease. The lease includes an option to extend the lease for an additional five-year period.
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v3.26.3
Composition of Other Balance Sheet Items - Schedule of Accrued Product Returns and Rebates (Details) - USD ($)
$ in Thousands
Sep. 30, 2026
Dec. 31, 2025
Organization, Consolidation and Presentation of Financial Statements [Abstract]    
Accrued product rebates $ 131,537 $ 123,297
Accrued product returns 33,811 37,800
Total $ 165,348 $ 161,097
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v3.26.3
Segment Reporting (Tables)
9 Months Ended
Sep. 30, 2026
Segment Reporting [Abstract]  
Schedule of Segment Reporting Information, by Segment
The following table shows the segment revenue, significant segment expenses and net earnings (dollars in thousands):
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)(unaudited)
Total revenues
$226,771 $192,103 $653,534 $507,380 
Less: Significant segment expenses:
Cost of revenues27,018 18,965 84,078 51,555 
Selling expenses
68,736 58,386 203,924 145,398 
Marketing expenses
21,778 18,672 66,356 60,068 
General and administrative expenses(a)
37,542 33,114 116,586 86,833 
Research and development expenses


Acquisition-related expenses— 69,506 — 70,874 
External development program expenses:
ONAPGO
58 352 834 1,613 
SPN-8203,507 1,111 8,324 8,073 
SPN-817(b)
4,215 4,872 27,715 11,889 
SPN-4431,113 773 2,159 1,799 
Qelbree1,899 3,168 6,480 9,805 
ZURZUVAE70 1,385 225 1,385 
Early-stage programs and other expenses
4,885 4,400 16,552 10,066 
Total external development program expenses
15,747 16,061 62,289 44,630 
Internal employee-related expenses
10,009 13,305 32,368 33,778 
Total research and development expenses
25,756 29,366 94,657 78,408 
Other segment items(c)
25,028 9,211 127,684 48,689 
Net earnings (loss)$20,913 $(45,117)$(39,751)$(34,445)
(a) Excludes Sage Acquisition related expenses which are presented in the separate line item, Acquisition-related expenses, in the table above.
(b) Includes amount related to Biscayne amendment. Refer to Note 17, Commitments and Contingencies.
(c) Other segment items include amortization of intangible assets, impairment charges, contingent consideration loss, net interest and other income, interest expense, and income tax expense (benefit) whose amounts are disclosed in the condensed consolidated statement of earnings (loss).
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v3.26.3
Subsequent Event (Details) - USD ($)
$ / shares in Units, $ in Millions
Oct. 30, 2026
Nov. 02, 2026
Oct. 31, 2026
Aug. 01, 2026
Acquisition Term Loan | Unsecured Debt | Invidior Pharmaceuticals, Inc.        
Subsequent Event [Line Items]        
Commitments to extend credit       $ 650
Subsequent Event        
Subsequent Event [Line Items]        
Common stock, dividends, per share, declared (in dollars per share) $ 8.13      
Subsequent Event | ONAPGO | Patents        
Subsequent Event [Line Items]        
Estimated useful lives     7 years  
Subsequent Event | Acquisition Term Loan | Unsecured Debt | Invidior Pharmaceuticals, Inc.        
Subsequent Event [Line Items]        
Commitments to extend credit   $ 650    
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v3.26.3
Sage Acquisition - Schedule of Purchase Price Allocation (Details) - USD ($)
$ in Thousands
5 Months Ended
Dec. 31, 2025
Jul. 31, 2025
Dec. 31, 2025
Sep. 30, 2026
Dec. 31, 2024
Business Combination [Line Items]          
Goodwill $ 124,882   $ 124,882 $ 119,431 $ 117,019
Fair value of contingent consideration 31,258   31,258 $ 206  
Sage Acquisition          
Business Combination [Line Items]          
Cash and cash equivalents 243,197 $ 243,197 243,197    
Marketable securities 93,181 93,181 93,181    
Accounts receivable, net 23,291 23,291 23,291    
Inventories, net 52,611 50,714 52,611    
Adjustment, Inventories, net     1,897    
Prepaid expenses and other current assets 16,580 18,674 16,580    
Adjustment, Prepaid expenses and other current assets     (2,094)    
Restricted cash 1,450 1,450 1,450    
Operating lease asset 5,110 5,630 5,110    
Adjustment, operating lease asset     (520)    
Intangible assets 142,900 166,500 142,900    
Adjustment, Intangible assets     (23,600)    
Deferred income tax assets, net 47,935   47,935    
Adjustment, deferred income tax assets, net     47,935    
Other assets 1,102 1,102 1,102    
Total fair value of assets acquired 627,357 603,739 627,357    
Adjustment, Total fair value of assets acquired     23,618    
Accounts payable and accrued liabilities 44,232 44,232 44,232    
Other liabilities 23,969   23,969    
Adjustment, other liabilities     23,969    
Operating lease liability 12,380 12,380 12,380    
Total fair value of liabilities assumed 80,581 56,612 80,581    
Adjustment, Total fair value of liabilities assumed     23,969    
Total identifiable net assets 546,776 547,127 546,776    
Adjustment, Total identifiable net assets     (351)    
Goodwill 2,412 2,061 2,412    
Adjustment, Goodwill     351    
Total purchase price 549,188 549,188 549,188    
Cash consideration paid for Sage's common stock   561,000      
Cash consideration paid for cash settlement of Sage's equity awards 4,073 4,073      
Fair value of contingent consideration 11,448 11,448 $ 11,448    
Sage Acquisition | Common Stock          
Business Combination [Line Items]          
Cash consideration paid for Sage's common stock $ 533,667 $ 533,667      
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v3.26.3
Collaboration Agreements
9 Months Ended
Sep. 30, 2026
Organization, Consolidation and Presentation of Financial Statements [Abstract]  
Collaboration Agreements Collaboration Agreements
Navitor
See Note 17, Commitments and Contingencies, for further details.
Shionogi
The Company is party to a collaboration and license agreement with Shionogi whereby Shionogi is responsible for all clinical development and regulatory filings for zuranolone in MDD and other indications in Japan, the Republic of Korea (South Korea), and Taiwan (together, the Shionogi Territory) and would be responsible for commercialization of zuranolone in the Shionogi Territory, to the extent zuranolone is successfully developed and obtains marketing approval in any of the countries within the Shionogi Territory. At the time of execution of the Shionogi Collaboration Agreement in 2018, Shionogi was required to make an upfront payment to Sage of $90.0 million, and the Company was eligible to receive additional payments of up to $470.0 million if certain regulatory and commercial milestones are achieved by Shionogi. As of September 30, 2026, the remaining potential future milestone payments include up to $40.0 million for the achievement of specified regulatory milestones, up to $10.0 million for the achievement of specified commercialization milestones, and up to $385.0 million for the achievement
of specified net sales milestones. The Company is also eligible to receive tiered royalties on sales of zuranolone in the Shionogi Territory, if development efforts are successful, with tiers averaging in the low to mid-twenty percent range, subject to other terms of the agreement. As between the Company and Shionogi, the Company maintains exclusive rights to develop and commercialize zuranolone outside of the Shionogi Territory. The upfront cash payment and any payments for milestones and royalties are non-refundable and non-creditable. Due to the uncertainty of pharmaceutical development and the high historical failure rates generally associated with drug development, the Company may not receive any milestone payments or any royalty payments from Shionogi. In the fourth quarter of 2025, Shionogi received approval from the Pharmaceuticals and Medical Devices Agency for the manufacturing and marketing of a product containing zuranolone in Japan for the treatment of MDD. Shionogi announced the first commercial sale of ZURZUVAE in Japan in the first quarter of 2026. No product containing zuranolone is approved for the treatment of MDD in the United States.

Under the clinical supply agreement, the Company is obligated to manufacture and supply to Shionogi (i) clinical quantities of API reasonably required by Shionogi for the development of licensed products in the Shionogi Territory under the collaboration and license agreement and (ii) quantities of drug product reasonably required for use by Shionogi in Phase 1 clinical trials of zuranolone in the Shionogi Territory under the collaboration and license agreement, in the quantities agreed to by the parties. A commercial supply agreement has not yet been entered into and the parties are operating under the provisions of the existing clinical supply agreement.

Biogen

Under the terms of the Biogen Collaboration Agreement, the Company granted Biogen a co-exclusive license to develop and commercialize SAGE-217 products in the U.S., an exclusive license to develop and commercialize SAGE-217 products in all countries of the world other than the U.S. and the Shionogi Territory. The Company refers to the territories outside the U.S. to which Biogen has rights under the Biogen Collaboration Agreement with respect to SAGE-217 as the Biogen Territory.

Development and commercialization activities in the U.S. under the Biogen Collaboration Agreement are conducted pursuant to plans agreed to by the Company and Biogen and overseen by a joint steering committee that consists of an equal number of representatives of each party. The Company and Biogen share equally in the costs for development and commercialization, as well as the profits and losses upon FDA approval and commencement of product sales, in the U.S., subject to the Company’s opt-out right described below. Biogen is solely responsible for all development activities and costs related to any development and commercialization of SAGE-217 products for the Biogen Territory, and the Company will receive royalties on any sales in the Biogen Territory, as mentioned above. Biogen is the principal and records sales of SAGE-217 products globally. The Company is obligated to supply API and bulk drug product for the Biogen Territory and API, bulk drug product and final drug product for the U.S. to support development and commercialization activities. Biogen has the right to assume manufacturing responsibilities for API for the Biogen Territory at any time during the term of the Biogen Collaboration Agreement, and the Biogen Collaboration Agreement further provides that Biogen will, within a reasonable period of time, assume manufacturing responsibility for bulk drug product for the Biogen Territory.

Unless terminated earlier, the Biogen Collaboration Agreement will continue on a country-by-country basis until the date on which (a) in any country in the Biogen Territory, the royalty term has expired in such country, and (b) for the U.S., the parties agree to permanently cease to commercialize. Biogen also has the right to terminate the Biogen Collaboration Agreement for convenience in its entirety or as to a particular region, upon advance written notice. The Company has an opt-out right to convert the co-exclusive license in the U.S. to an exclusive license to Biogen. Following the exercise of the opt-out right, the Company would no longer share equally in the profits and losses in the U.S. and would be entitled to receive certain royalty payments at percentage rates ranging from the low to high twenties and additional sales milestones.

While Biogen is considered the principal in transactions with customers for the sale of ZURZUVAE globally, the Company is also engaged in significant commercialization activities, including maintaining its own U.S. direct sales force. The Company presents its proportionate share of Biogen’s ZURZUVAE sales to customers in the U.S. as Collaboration revenue (ZURZUVAE) within the condensed consolidated statements of earnings (loss). Payments to or reimbursements from Biogen related to the agreement of the parties to share equally in all revenue and costs are accounted for as an increase to Collaboration revenue (ZURZUVAE), an increase to or reduction of Cost of revenues, Research and development expenses, or Selling, general and administrative expenses, in the condensed consolidated statements of earnings (loss), depending on the nature of the activity.

To record its proportionate share of collaboration revenue from Biogen’s sales of ZURZUVAE to customers in the U.S., the Company utilizes certain information from Biogen, including revenue from the sale of the product and associated reserves on revenue.
The following table summarizes the Company’s proportionate share of the activity under the Biogen Collaboration Agreement:
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)
(unaudited)
Collaboration revenue (ZURZUVAE)
$41,697 $20,164 $104,690 $20,164 
Cost of revenues
641 434 2,967 434 
Research and development expenses
504 (928)1,797 (928)
Selling, general and administrative expenses
27,998 13,561 77,907 13,561 
Amounts receivable from Biogen related to the Biogen Collaboration Agreement are recorded within Accounts receivable, net on the condensed consolidated balance sheets and were $49.5 million and $23.0 million as of September 30, 2026 and December 31, 2025, respectively.
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9 Months Ended
Sep. 30, 2026
segment
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v3.26.3
Disaggregated Revenues - Schedule of Disaggregation of Revenue by Nature (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2026
Sep. 30, 2025
Sep. 30, 2026
Sep. 30, 2025
Disaggregation of Revenue [Line Items]        
Total revenues $ 226,771 $ 192,103 $ 653,534 $ 507,380
Net product sales        
Disaggregation of Revenue [Line Items]        
Total revenues 178,576 168,542 495,042 468,525
Qelbree        
Disaggregation of Revenue [Line Items]        
Total revenues 90,824 81,416 257,906 223,708
GOCOVRI        
Disaggregation of Revenue [Line Items]        
Total revenues 42,650 40,849 115,420 108,198
ONAPGO        
Disaggregation of Revenue [Line Items]        
Total revenues 17,075 6,806 38,996 8,410
Trokendi XR        
Disaggregation of Revenue [Line Items]        
Total revenues 10,213 10,043 28,103 34,037
Oxtellar XR        
Disaggregation of Revenue [Line Items]        
Total revenues 7,957 12,016 24,161 33,851
APOKYN        
Disaggregation of Revenue [Line Items]        
Total revenues 6,490 10,387 20,541 38,183
Other        
Disaggregation of Revenue [Line Items]        
Total revenues 3,367 7,025 9,915 22,138
Collaboration revenue (ZURZUVAE)        
Disaggregation of Revenue [Line Items]        
Total revenues 41,697 20,164 104,690 20,164
Royalty, licensing, and other revenues        
Disaggregation of Revenue [Line Items]        
Total revenues $ 6,498 $ 3,397 $ 53,802 $ 18,691
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v3.26.3
Leases (Tables)
9 Months Ended
Sep. 30, 2026
Leases [Abstract]  
Schedule of Balance Sheet Information Related to Leases
Operating lease assets and lease liabilities as reported on the condensed consolidated balance sheets are as follows (dollars in thousands):

Balance Sheet ClassificationSeptember 30, 2026December 31, 2025
(unaudited)
Assets
Operating lease assetsOther assets$23,059 $26,712 
Total lease assets$23,059 $26,712 
Liabilities
Operating lease liabilities, current portionAccounts payable and accrued liabilities$7,620 $10,612 
Operating lease liabilities, long-termOperating lease liabilities, long-term28,577 30,365 
Total lease liabilities$36,197 $40,977 
Schedule of Supplemental Cash Flow Information
Supplemental cash flow information related to leases is as follows (dollars in thousands):
Nine Months Ended
September 30,
20262025
(unaudited)
Cash paid for operating leases$17,411 $14,415 
Lease assets obtained for new operating leases4,569 9,941 
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v3.26.3
Composition of Other Balance Sheet Items - Schedule of Property and Equipment (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2026
Sep. 30, 2025
Sep. 30, 2026
Sep. 30, 2025
Dec. 31, 2025
Property and equipment          
Subtotal $ 29,593   $ 29,593   $ 28,795
Less accumulated depreciation and amortization (19,572)   (19,572)   (18,264)
Property and equipment, net 10,021   10,021   10,531
Depreciation and amortization expense 400 $ 500 1,300 $ 1,600  
Lab equipment and furniture          
Property and equipment          
Subtotal 14,538   14,538   14,041
Leasehold improvements          
Property and equipment          
Subtotal 13,052   13,052   13,052
Software          
Property and equipment          
Subtotal 951   951   871
Computer equipment          
Property and equipment          
Subtotal $ 1,052   $ 1,052   $ 831
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v3.26.3
Collaboration Agreements - Narrative (Details) - USD ($)
$ in Thousands
Sep. 30, 2026
Dec. 31, 2025
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]    
Accounts receivable, net $ 214,714 $ 187,802
Biogen Collaboration Agreement    
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]    
Accounts receivable, net 49,500 $ 23,000
Shionogi | License    
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]    
Contract liabilities 90,000  
Revenue, remaining performance obligation, variable consideration amount 470,000  
Shionogi | License | Achievement Of Specified Regulatory Milestones    
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]    
Revenue, remaining performance obligation, variable consideration amount 40,000  
Shionogi | License | Achievement Of Specified Commercialization Milestones    
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]    
Revenue, remaining performance obligation, variable consideration amount 10,000  
Shionogi | License | Achievement Of Specified Net Sales Milestones    
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]    
Revenue, remaining performance obligation, variable consideration amount $ 385,000  
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Leases - Supplemental Cash Flows (Details) - USD ($)
$ in Thousands
9 Months Ended
Sep. 30, 2026
Sep. 30, 2025
Leases [Abstract]    
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Lease assets obtained for new operating leases $ 4,569 $ 9,941
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Sep. 30, 2025
Disaggregation of Revenue [Line Items]    
Prior year sale adjustments, percentage (1.00%) (4.00%)
Shionogi | License    
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Revenue recognized $ 20.0  
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v3.26.3
Share-Based Payments - Schedule of Stock Option (Details) - $ / shares
9 Months Ended 12 Months Ended
Sep. 30, 2026
Dec. 31, 2025
Number of Options    
Outstanding at the beginning of the period (in shares) 6,343,009  
Granted (in shares) 988,592  
Exercised (in shares) (565,366)  
Forfeited (in shares) (124,726)  
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Vested and expected to vest (in dollars per share) 35.22 32.63
Exercisable (in dollars per share) $ 32.46 $ 32.08
Weighted Average Remaining Contractual Term (in years)    
Outstanding at the end of the period 6 years 2 months 12 days 6 years 3 months 18 days
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Exercisable 4 years 9 months 18 days 4 years 9 months 18 days
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Goodwill and Intangible Assets, Net (Tables)
9 Months Ended
Sep. 30, 2026
Intangible Asset, Goodwill and Other [Abstract]  
Schedule of Goodwill
The following table sets forth the gross carrying amounts of goodwill (dollars in thousands)
September 30,
2026
December 31,
2025
(unaudited)
Beginning balance$124,882 $117,019 
Goodwill activity from Sage Acquisition (a)
(5,451)7,863 
Ending balance
$119,431 $124,882 
(a) Refer to Note 3, Sage Acquisition for further detail.
Schedule of Intangible Assets, Net
The following table sets forth the gross carrying amounts and related accumulated amortization of intangible assets subject to amortization (dollars in thousands):
September 30, 2026December 31, 2025
(unaudited)
Remaining Weighted
Average Life (Years)
Carrying Amount, GrossAccumulated AmortizationCarrying Amount, NetCarrying Amount, GrossAccumulated AmortizationCarrying Amount, Net
Acquired developed technology and product rights5.7$873,291 $(427,053)$446,238 $922,311 $(352,855)$569,456 
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v3.26.3
Share-Based Payments - Narrative (Details) - USD ($)
$ in Millions
1 Months Ended
Jun. 30, 2026
Sep. 30, 2026
Sage Acquisition    
Share-based payments    
Unrecognized compensation expense   $ 12.3
2021 Equity Incentive Plan    
Share-based payments    
Number of additional shares authorized (in shares) 4,000,000  
Maximum number of shares of common stock provided for issuance (in shares)   19,012,893
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v3.26.3
Earnings (Loss) per Share
9 Months Ended
Sep. 30, 2026
Earnings Per Share [Abstract]  
Earnings (Loss) per Share Earnings (Loss) per Share
The following table sets forth the computation of basic and diluted earnings per share for the three and nine months ended September 30, 2026 and 2025 (dollars in thousands, except share and per share amounts):
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)(unaudited)
Numerator:
Net earnings (loss)$20,913 $(45,117)$(39,751)$(34,445)
Numerator for basic and dilutive earnings (loss) per share$20,913 $(45,117)$(39,751)$(34,445)
Denominator:
Weighted average shares outstanding, basic58,202,474 56,552,741 57,975,499 56,133,918 
Effect of dilutive securities:
Stock options and stock awards1,268,547 — — — 
Weighted average shares outstanding, diluted59,471,021 56,552,741 57,975,499 56,133,918 
Earnings (loss) per share, basic$0.36 $(0.80)$(0.69)$(0.61)
Earnings (loss) per share, diluted$0.35 $(0.80)$(0.69)$(0.61)
The following table sets forth the common stock equivalents of outstanding stock-based awards excluded in the calculation of diluted earnings (loss) per share, because the vesting conditions have not been met as of the end of the reporting period or their inclusion would be anti-dilutive:
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)(unaudited)
Stock options and stock awards496,023 647,044 7,449,141 743,145 
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v3.26.3
Segment Reporting - Narrative (Details)
9 Months Ended
Sep. 30, 2026
segment
Segment Reporting [Abstract]  
Number of operating segments 1
Number of reportable segments 1
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Segment Reporting - Schedule of Segment Reporting Information (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2026
Jun. 30, 2026
Mar. 31, 2026
Sep. 30, 2025
Jun. 30, 2025
Mar. 31, 2025
Sep. 30, 2026
Sep. 30, 2025
Segment Reporting [Line Items]                
Total revenues $ 226,771     $ 192,103     $ 653,534 $ 507,380
Cost of revenues [1] 27,018     18,965     84,078 51,555
Acquisition-related expenses 0     69,506     0 70,874
Total research and development expenses 25,756     29,366     94,657 78,408
Net earnings (loss) 20,913 $ (58,371) $ (2,293) (45,117) $ 22,499 $ (11,827) (39,751) (34,445)
Reportable Segment                
Segment Reporting [Line Items]                
Total revenues 226,771     192,103     653,534 507,380
Cost of revenues 27,018     18,965     84,078 51,555
Selling expenses 68,736     58,386     203,924 145,398
Marketing expenses 21,778     18,672     66,356 60,068
General and administrative expenses 37,542     33,114     116,586 86,833
Total external development program expenses 15,747     16,061     62,289 44,630
Internal employee-related expenses 10,009     13,305     32,368 33,778
Total research and development expenses 25,756     29,366     94,657 78,408
Other segment items 25,028     9,211     127,684 48,689
Net earnings (loss) 20,913     (45,117)     (39,751) (34,445)
Reportable Segment | ONAPGO                
Segment Reporting [Line Items]                
Total external development program expenses 58     352     834 1,613
Reportable Segment | SPN-820                
Segment Reporting [Line Items]                
Total external development program expenses 3,507     1,111     8,324 8,073
Reportable Segment | SPN-817                
Segment Reporting [Line Items]                
Total external development program expenses 4,215     4,872     27,715 11,889
Reportable Segment | SPN-443                
Segment Reporting [Line Items]                
Total external development program expenses 1,113     773     2,159 1,799
Reportable Segment | Qelbree                
Segment Reporting [Line Items]                
Total external development program expenses 1,899     3,168     6,480 9,805
Reportable Segment | ZURZUVAE                
Segment Reporting [Line Items]                
Total external development program expenses 70     1,385     225 1,385
Reportable Segment | Early-stage programs and other expenses                
Segment Reporting [Line Items]                
Total external development program expenses $ 4,885     $ 4,400     $ 16,552 $ 10,066
[1] Excludes amortization of intangible assets
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v3.26.3
Condensed Consolidated Balance Sheets - USD ($)
$ in Thousands
Sep. 30, 2026
Dec. 31, 2025
Current assets    
Cash and cash equivalents $ 175,884 $ 128,448
Marketable securities 183,575 180,222
Accounts receivable, net 214,714 187,802
Inventories, net 87,112 82,385
Prepaid expenses and other current assets 49,930 65,325
Total current assets 711,215 644,182
Restricted cash 1,450 1,450
Property and equipment, net 10,021 10,531
Intangible assets, net 446,238 569,456
Goodwill 119,431 124,882
Deferred income tax assets, net 54,317 38,351
Other assets 55,018 63,796
Total assets 1,397,690 1,452,648
Current liabilities    
Accounts payable and accrued liabilities 109,136 107,800
Accrued product returns and rebates 165,348 161,097
Contingent consideration, current portion 0 31,052
Other current liabilities 10,913 38,222
Total current liabilities 285,397 338,171
Contingent consideration, long-term 206 206
Operating lease liabilities, long-term 28,577 30,365
Other liabilities 21,032 22,192
Total liabilities 335,212 390,934
Commitments and contingencies (Note 17)
Stockholders' equity    
Common stock, $0.001 par value; 130,000,000 shares authorized; 58,254,131 and 57,457,462 shares issued and outstanding as of September 30, 2026 and December 31, 2025, respectively 58 57
Additional paid-in capital 584,575 543,825
Accumulated other comprehensive loss, net of tax (280) (44)
Retained earnings 478,125 517,876
Total stockholders' equity 1,062,478 1,061,714
Total liabilities and stockholders' equity $ 1,397,690 $ 1,452,648
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v3.26.3
Share-Based Payments (Tables)
9 Months Ended
Sep. 30, 2026
Share-Based Payment Arrangement [Abstract]  
Schedule of Share-Based Compensation Expense
Share-based compensation expense is as follows (dollars in thousands):
Three Months Ended
September 30,
Nine Months Ended
September 30,
2026202520262025
(unaudited)(unaudited)
Research and development$1,525 $1,446 $4,449 $4,337 
Selling, general and administrative(a)
7,408 29,299 21,604 41,983 
Total$8,933 $30,745 $26,053 $46,320 
(a) The prior period includes $22.9 million of compensation expense related to the acceleration of certain Sage equity awards in connection with the Sage Acquisition in July 2025.
Schedule of Stock Options
The following table summarizes stock option activities:
Number of
Options
Weighted
Average
Exercise Price
Weighted
Average
Remaining
Contractual
Term (in years)
Outstanding, December 31, 20256,343,009 $32.63 6.3
Granted 988,592 $49.93 
Exercised (565,366)$31.00 
Forfeited (124,726)$39.06 
Outstanding, September 30, 2026 (unaudited)6,641,509 $35.22 6.2
As of September 30, 2026 (unaudited):
Vested and expected to vest6,641,509 $35.22 6.2
Exercisable 4,053,054 $32.46 4.8
As of December 31, 2025:
Vested and expected to vest6,343,009 $32.63 6.3
Exercisable3,636,073 $32.08 4.8
Schedule of Restricted Stock Units
The following table summarizes restricted stock unit (RSU) activities:
Number of
RSUs
Weighted Average
Grant Date Fair Value per Share
Nonvested, December 31, 2025396,693 $32.98 
Granted122,609 $50.20 
Vested(165,678)$33.43 
Forfeited(11,375)$37.89 
Nonvested, September 30, 2026 (unaudited)342,249 $38.77 
Schedule of Performance Stock Unit
The following table summarizes performance share unit (PSU) activities:
Number of PSUsWeighted
Average
Grant Date Fair Value per Share
Nonvested, December 31, 2025390,496 $30.80 
Granted236,466 $47.73 
Vested(103,989)$29.43 
Forfeited(57,590)$28.33 
Nonvested, September 30, 2026 (unaudited)465,383$40.01 
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