Supernus Pharmaceuticals Reports Second Quarter 2012 Financial Results
ROCKVILLE, Md., Aug. 10, 2012 (GLOBE NEWSWIRE) -- Supernus Pharmaceuticals, Inc. (SUPN), a specialty pharmaceutical company, today reported consolidated financial results for the three and six months ending June 30, 2012, and provided an update on key accomplishments to date and expected milestones for 2012.
Jack A. Khattar, President and CEO of Supernus stated, "This has been an exciting and eventful quarter for the Company. We completed our IPO in May, raising net proceeds of $47.6 million and, in June, received tentative approval from the FDA for our lead product Trokendi XRTM. "
Second quarter 2012 Financial Results
- Cash, cash equivalents and unrestricted marketable securities of $76.4 million at June 30, 2012.
- Research and development (R&D) expense for second quarter 2012 was $4.7 million compared with $7.3 million in 2011. The decrease was primarily due to the conclusion of the SPN-538 and SPN-804 clinical trials in 2011.
- Selling, general and administrative (SG&A) expense for second quarter 2012 was $4.6 million compared with $1.9 million in 2011. The increase was primarily due to higher sales and marketing infrastructure expenses, as we prepare to launch SPN-804 and Trokendi XR.
- Net loss applicable to common shareholders for second quarter 2012 was $10.3 million or $0.61 per common share (based on 16.8 million weighted average diluted shares outstanding), compared with $8.2 million, or $5.17 per common share, for 2011 (based on 1.6 million weighted average diluted shares outstanding). Net loss per share decreased due to the significant number of common shares issued in May 2012 in connection with our IPO.
Six months ending June 30, 2012 Financial Results
- R&D expense for the first half of 2012 was $10.1 million compared with $14.7 million in 2011. The decrease was primarily due to the conclusion of the SPN-804 and Trokendi XR clinical trials in 2011.
- SG&A expense for the first half of 2012 was $7.4 million compared with $3.6 million in 2011. The increase was primarily due to higher sales and marketing infrastructure expenses, as we prepare to launch SPN-804 and Trokendi XR.
- Net loss applicable to common shareholders for the first half of 2012 was $20.4 million or $2.21 per common share (based on 9.2 million weighted average diluted shares outstanding), compared with $20.1million, or $12.64 per common share, for 2011 (based on 1.6 million weighted average diluted shares outstanding). Net loss per share decreased due to the significant number of common shares issued in May 2012 in connection with our IPO.
Liquidity and Capital Resources
Our anticipated cash burn for 2012 is estimated to be in the range of $55 million to $60 million due to the change in timing of the planned launch of Trokendi XR from year-end 2012 to third quarter of 2013. Based on our current plans, Supernus continues to anticipate that our current cash, cash equivalents and unrestricted marketable securities as of June 30, 2012 should be sufficient to fund operations into the second quarter of 2013.
About Supernus Pharmaceuticals, Inc.
Supernus Pharmaceuticals, Inc. is a specialty pharmaceutical company focused on developing and commercializing products for the treatment of central nervous system, or CNS, diseases. The company is developing several product candidates in neurology and psychiatry to address large market opportunities in epilepsy and ADHD including ADHD patients with impulsive aggression. These product candidates include Trokendi XR (extended-release topiramate), formerly known as SPN-538, and SPN-804 (extended-release oxcarbazepine) for epilepsy, SPN-810 for impulsive aggression in ADHD and SPN-812 for ADHD.
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 achieve profitability; the Company's ability to raise sufficient capital to 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 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 respective PDUFA dates for 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 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 SEC filings made pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934, as amended. The Company undertakes no obligation to update the information in this press release to reflect events or circumstances after the date hereof or to reflect the occurrence of anticipated or unanticipated events.
|SUPERNUS PHARMACEUTICS, INC.|
|CONDENSED CONSOLIDATED BALANCE SHEETS|
|December, 31||June 30,|
|Cash, cash equivalents and marketable securities||$ 48,544||$ 76,392|
|Other current assets||855||1,413|
|Total current assets||49,399||77,805|
|Property and equipment, net||1,310||1,146|
|Deferred financing costs||2,054||161|
|Other long-term assets||967||853|
|Accounts payable and accrued expenses||$ 11,625||$ 10,510|
|Secured notes payable, current||6,775||10,747|
|Other current liabilities||370||624|
|Total current liabilities||18,770||21,881|
|Secured notes payable, long-term||22,711||17,061|
|Total Stockholders' Equity||9,443||37,980|
|Total Liabilities & Stockholders Equity||$ 53,730||$ 79,965|
|SUPERNUS PHARMACEUTICS, INC.|
|CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS|
|(in thousands, except per share data)|
|Three months ended||Six months ended|
|June 30, 2011||June 30, 2012||June 30, 2011||June 30, 2012|
|Total revenues||$ 750||$ 91||$ 750||$ 299|
|Research and development||7,251||4,703||14,702||10,061|
|General and administrative||1,895||4,645||3,642||7,374|
|Total operating expenses||9,146||9,348||18,344||17,435|
|Other income (expense):|
|Net loss from continuing operations||(8,940)||(10,013)||(18,655)||(19,288)|
|Net loss||$ (7,377)||$ (10,013)||$ (18,426)||$ (19,288)|
|Cumulative Dividends on Preferred Stock||$ (858)||$ (286)||$ (1,715)||$ (1,143)|
|Net loss attributable to common shareholders||$ (8,235)||$ (10,299)||$ (20,141)||$ (20,431)|
|Net loss per share - basic & diluted||$ (5.17)||$ (0.61)||$ (12.64)||$ (2.21)|
|Weighted average number of shares outstanding (post-split)||1,594,246||16,817,841||1,593,508||9,247,142|
CONTACT: Jack Khattar, President & CEO Gregory S. Patrick, Vice President and CFO Supernus Pharmaceuticals, Inc. Tel: (301) 838-2591Source: Supernus Pharmaceuticals, Inc. 2012 GlobeNewswire, Inc.