Supernus Announces Third Quarter 2018 Financial Results and Record Quarterly Revenue
- Total revenue of
$103.0 million , a 28% increase over 2017 - Net product sales of
$100.2 million , a 28% increase over 2017 - Operating earnings of
$37.5 million , a 68% increase over 2017 - Diluted earnings per share (GAAP) of
$0.52 , a 79% increase over 2017 - Data from first three Phase III SPN-812 trials expected in
December 2018 - Acquisition of
Biscayne Neurotherapeutics, Inc. closed inOctober 2018 - Ranked #1 fastest growing pharmaceutical company worldwide per Fortune 100 fastest growing companies
Commercial Update
Third quarter 2018 product prescriptions for Trokendi XR® and Oxtellar XR®, as reported by
| Prescriptions | ||||
| Q3 2018 | Q3 2017 | Change % | ||
| Trokendi XR | 182,268 | 145,762 | 25.0% | |
| Oxtellar XR | 39,587 | 35,129 | 12.7% | |
| Total | 221,855 | 180,891 | 22.6% | |
Source:
Net product sales for the third quarter of 2018 were
| Net Product Sales ($ in millions) | |||||||
| Q3 2018 | Q3 2017 | Change % | |||||
| Trokendi XR | $79.8 | $59.4 | 34.3% | ||||
| Oxtellar XR | $20.4 | $18.7 | 9.1% | ||||
| Total | $100.2 | $78.1 | 28.3% | ||||
“Supernus generated another strong quarter of growth, setting a new record for quarterly net product sales of
Given the recently accelerated development timeline for SPN-812 that positions its potential regulatory approval and commercial launch ahead of SPN-810, the Company has directed its resources to prioritize filing of the New Drug Application (NDA) and potential commercial launch of SPN-812 in
As a result, the following are the updated plans and timelines for both product candidates:
SPN-812 – Novel non-stimulant for the treatment of ADHD
- The Phase III program consists of four three-arm, placebo-controlled trials: P301 and P303 trials in patients 6-11 years old and P302 and P304 trials in patients 12-17 years old.
- The Company expects to announce top-line data from P301 and P303 pediatric trials concurrently in early
December 2018 , and from P302, the first adolescent Phase III trial, by the end ofDecember 2018 . Top-line data from the second adolescent Phase III trial, P304, are expected by the end of the first quarter of 2019. - The Company expects to submit an NDA for SPN-812 in the second half of 2019, and to launch it, pending
U.S. Food and Drug Administration (FDA ) approval, in the second half of 2020.
SPN-810 – Treatment of Impulsive Aggression in patients with ADHD
- As expected, the first Phase III trial (P301) has reached its original enrollment target. However, given the aforementioned prioritization of SPN-812 and that top-line data from the second Phase III trial (P302) is expected around mid-2019, the Company has decided to keep P301 enrollment active until data from both trials can be released concurrently instead of sequentially. This change does not impact the timing of submission of the NDA for SPN-810, given that the NDA submission is rate-limited by completion of the P302 trial and generation of data in the adolescent patient population.
- The Company continues to observe enrollment in the open label extension (OLE) study at 90% or higher. On average, a patient in the OLE study remains on SPN-810 treatment for 9.5 months, which we believe is an encouraging sign of the tolerability and efficacy of SPN-810.
- Patient dosing has been initiated in the Phase III trial in adolescent patients.
- The Company expects to submit an NDA for SPN-810 in the second half of 2020, and to launch it, pending
FDA approval, in the second half of 2021.
SPN-604 (formerly known as Oxtellar XR for Bipolar)
- The Company continues to expect initiating pivotal Phase III studies for the treatment of bipolar disorder in the second half of 2019.
“We are pleased to announce the completion of enrollment in the first three Phase III trials for SPN-812,” said
Operating Expenses
Research and development expenses in the third quarter of 2018 were
Selling, general and administrative expenses in the third quarter of 2018 were
Operating Earnings and Earnings Per Share
Operating earnings in the third quarter of 2018 were
GAAP net earnings in the third quarter of 2018 were
Weighted-average diluted common shares outstanding were approximately 54.2 million in the third quarter of 2018, as compared to approximately 53.6 million in the third quarter of 2017.
As of
Financial Guidance
For full year 2018, the Company is updating its prior guidance as set forth below:
- Net product sales in the range of
$388 million to $395 million , compared to the previously expected range of $385 million to $400 million. - Research and development expenses of approximately
$95 million , including the one-time upfront expense of $15 million in the fourth quarter for the acquisition ofBiscayne Neurotherapeutics, Inc. - Operating earnings in the range of
$120 million to $125 million , compared to the previously expected range of $115 million to $125 million. - The Company expects an effective tax rate of approximately 23% to 25% for the fourth quarter of 2018.
Supernus ranked number one pharmaceutical company worldwide in Fortune’s “100 Fastest-Growing Companies” list for 2018 and number three in all industries
In
To view the full list of Fortune’s 100 Fastest-Growing Companies go to: http://fortune.com/100-fastest-growing-companies.
“I am so proud of our employees. They deserve all the recognition Supernus has received over the past few years, from making the Deloitte Technology Fast 500 list three years in a row to being ranked as the number one Fortune 100 fastest growing pharmaceutical company in the world,” said
Conference Call Details
The Company will hold a conference call hosted by
Please refer to the information below for conference call dial-in information and webcast registration. Callers should dial in approximately 10 minutes prior to the start of the call.
| Conference dial-in: International dial-in: Conference ID: Conference Call Name: |
(877) 288-1043 (970) 315-0267 2697616 Supernus Pharmaceuticals Third Quarter 2018 Earnings Conference Call |
|
Following the live call, a replay will be available on the Company's website, www.supernus.com, under “Investor Relations”.
About
Forward-Looking Statements:
This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These statements do not convey historical information, but relate to predicted or potential future events that are based upon management's current expectations. These statements are subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. In addition to the factors mentioned in this press release, such risks and uncertainties include, but are not limited to, the Company’s ability to sustain and increase its profitability; the Company’s ability to raise sufficient capital to fully implement its corporate strategy; the implementation of the Company’s corporate strategy; the Company’s future financial performance and projected expenditures; the Company’s ability to increase the number of prescriptions written for each of its products; the Company’s ability to increase its net revenue; the Company’s ability to enter into future collaborations with pharmaceutical companies and academic institutions or to obtain funding from government agencies; the Company’s product research and development activities, including the timing and progress of the Company’s clinical trials, and projected expenditures; the Company’s ability to receive, and the timing of any receipt of, regulatory approvals to develop and commercialize the Company’s product candidates; the Company’s ability to protect its intellectual property and operate its business without infringing upon the intellectual property rights of others; the Company’s expectations regarding federal, state and foreign regulatory requirements; the therapeutic benefits, effectiveness and safety of the Company’s product candidates; the accuracy of the Company’s estimates of the size and characteristics of the markets that may be addressed by its product candidates; the Company’s ability to increase its manufacturing capabilities for its products and product candidates; the Company’s projected markets and growth in markets; the Company’s product formulations and patient needs and potential funding sources; the Company’s staffing needs; and other risk factors set forth from time to time in the Company’s filings with the
| Supernus Pharmaceuticals, Inc. | ||||||||
| Consolidated Balance Sheets | ||||||||
| (in thousands, except share amounts) | ||||||||
| September 30, | December 31, | |||||||
| 2018 | 2017 | |||||||
| Assets | (unaudited) | |||||||
| Current assets | ||||||||
| Cash and cash equivalents | $ | 123,818 | $ | 100,304 | ||||
| Marketable securities | 156,407 | 39,736 | ||||||
| Accounts receivable, net | 77,753 | 65,586 | ||||||
| Inventories, net | 23,280 | 16,304 | ||||||
| Prepaid expenses and other current assets | 9,299 | 6,521 | ||||||
| Total current assets | 390,557 | 228,451 | ||||||
| Long term marketable securities | 460,304 | 133,638 | ||||||
| Property and equipment, net | 6,930 | 5,124 | ||||||
| Intangible assets, net | 32,572 | 36,019 | ||||||
| Deferred income taxes | 31,367 | 20,843 | ||||||
| Other non-current assets | 782 | 389 | ||||||
| Total assets | $ | 922,512 | $ | 424,464 | ||||
| Liabilities and stockholders' equity | ||||||||
| Current liabilities | ||||||||
| Accounts payable | $ | 9,838 | $ | 6,844 | ||||
| Accrued sales deductions | 85,970 | 68,343 | ||||||
| Accrued expenses | 32,098 | 27,305 | ||||||
| Income taxes payable | 8,548 | 15,938 | ||||||
| Non-recourse liability related to sale of future royalties, current portion | 1,892 | 4,283 | ||||||
| Deferred licensing revenue | — | 287 | ||||||
| Total current liabilities | 138,346 | 123,000 | ||||||
| Deferred licensing revenue, net of current portion | — | 1,149 | ||||||
| Convertible notes, net | 325,666 | — | ||||||
| Non-recourse liability related to sale of future royalties, long term | 23,305 | 22,258 | ||||||
| Other non-current liabilities | 13,259 | 10,577 | ||||||
| Total liabilities | 500,576 | 156,984 | ||||||
| Stockholders' equity | ||||||||
| Common stock, $0.001 par value, 130,000,000 shares authorized at September 30, 2018 and December 31, 2017; 52,257,013 and 51,314,850 shares issued and outstanding at September 30, 2018 and December 31, 2017, respectively | 52 | 51 | ||||||
| Additional paid-in capital | 365,396 | 294,999 | ||||||
| Accumulated other comprehensive loss, net of tax | (4,111 | ) | (747 | ) | ||||
| Retained earnings (accumulated deficit) | 60,599 | (26,823 | ) | |||||
| Total stockholders' equity | 421,936 | 267,480 | ||||||
| Total liabilities and stockholders' equity | $ | 922,512 | $ | 424,464 | ||||
| Supernus Pharmaceuticals, Inc. | |||||||||||||||
| Consolidated Statements of Earnings | |||||||||||||||
| (in thousands, except share and per share data) | |||||||||||||||
| Three Months ended September 30, | Nine Months ended September 30, | ||||||||||||||
| 2018 | 2017 | 2018 |
2017 | ||||||||||||
| (unaudited) | (unaudited) | ||||||||||||||
| Revenue | |||||||||||||||
| Net product sales | $ | 100,227 | $ | 78,066 | $ | 286,377 | $ | 207,763 | |||||||
| Royalty revenue | 2,769 | 2,010 | 5,836 | 4,338 | |||||||||||
| Licensing revenue | — | 322 | 750 | 1,702 | |||||||||||
| Total revenue | 102,996 | 80,398 | 292,963 | 213,803 | |||||||||||
| Costs and expenses | |||||||||||||||
| Cost of product sales | 4,207 | 4,251 | 11,168 | 11,060 | |||||||||||
| Research and development | 20,422 | 12,980 | 59,368 | 33,405 | |||||||||||
| Selling, general and administrative | 40,892 | 40,825 | 117,838 | 104,141 | |||||||||||
| Total costs and expenses | 65,521 | 58,056 | 188,374 | 148,606 | |||||||||||
| Operating earnings | 37,475 | 22,342 | 104,589 | 65,197 | |||||||||||
| Other income (expense) | |||||||||||||||
| Interest income | 4,461 | 814 | 9,331 | 2,002 | |||||||||||
| Interest expense | (4,374 | ) | — | (9,415 | ) | (148 | ) | ||||||||
| Interest expense-nonrecourse liability related to sale of future royalties | (1,191 | ) | (155 | ) | (3,096 | ) | (1,274 | ) | |||||||
| Changes in fair value of derivative liabilities | — | — | — | 76 | |||||||||||
| Loss on extinguishment of debt | — | (91 | ) | — | (295 | ) | |||||||||
| Total other income (expense) | (1,104 | ) | 568 | (3,180 | ) | 361 | |||||||||
| Earnings before income taxes | 36,371 | 22,910 | 101,409 | 65,558 | |||||||||||
| Income tax expense | 8,360 | 6,949 | 16,309 | 21,932 | |||||||||||
| Net earnings | $ | 28,011 | $ | 15,961 | $ | 85,100 | $ | 43,626 | |||||||
| Earnings per share: | |||||||||||||||
| Basic | $ | 0.54 | $ | 0.31 | $ | 1.64 | $ | 0.86 | |||||||
| Diluted | $ | 0.52 | $ | 0.29 | $ | 1.57 | $ | 0.82 | |||||||
| Weighted-average number of common shares outstanding: | |||||||||||||||
| Basic | 52,227,630 | 51,046,375 | 51,897,240 | 50,583,726 | |||||||||||
| Diluted | 54,239,847 | 53,628,389 | 54,098,330 | 53,227,433 | |||||||||||
CONTACTS:
Tel: (301) 838-2591
or
INVESTOR CONTACT:
Westwicke Partners
Office: (443) 213-0505
Mobile: (443) 377-4767
Email: peter.vozzo@westwicke.com
Source: Supernus Pharmaceuticals, Inc.