EMERYVILLE, Calif., Feb. 28, 2017 (GLOBE NEWSWIRE) -- Adamas Pharmaceuticals, Inc. (Nasdaq:ADMS) today reported recent achievements and financial results for the fourth quarter and full-year ended December 31, 2016.
“We expect 2017 to be a pivotal year as we transform from an R&D-focused company to a commercial organization as we anticipate FDA approval of ADS-5102 for the treatment of levodopa-induced dyskinesia. If approved, we expect to launch ADS-5102 in the second half of 2017, providing Parkinson’s patients with the first and only medicine indicated for the treatment of levodopa-induced dyskinesia,” said Gregory T. Went, Ph.D., Chairman and Chief Executive Officer of Adamas Pharmaceuticals, Inc. “In addition, we are continuing to develop ADS-5102 in additional indications, as well as to advance the clinical development of ADS-4101 for the treatment of partial onset seizures in patients with epilepsy, the fourth chrono-synchronous targeted therapy to emerge from our drug development platform.”
ADS-5102 (amantadine hydrochloride) extended release capsules
- Acceptance of the New Drug Application (NDA) for ADS-5102 for the treatment of levodopa-induced dyskinesia (LID) in patients with Parkinson’s disease by the U.S. Food and Drug Administration (FDA); the PDUFA date is August 24, 2017
- Presented an updated analysis from EASE LID 2, the open-label, long-term safety study of ADS-5102 in Parkinson’s disease patients with LID, at the First Pan American Parkinson’s Disease and Movement Disorders Congress. The updated analysis showed the safety and tolerability of ADS-5102 and treatment effect on LID and OFF time with ADS-5102 up to 64 weeks, as measured by Part IV (Motor Complications) of the Movement Disorder Society-Unified Parkinson’s Disease Rating Scale (MDS-UPDRS)
- Participated in a productive End-of-Phase 2 meeting with the FDA regarding the Phase 3 development pathway for ADS-5102 for the treatment of walking impairment in patients with multiple sclerosis
- Presented data from a Phase 2 proof-of-concept study of ADS-5102 for the treatment of walking impairment in patients with multiple sclerosis at the American Committee for the Treatment and Research of Multiple Sclerosis (ACTRIMS), highlighting treatment effect in several performance measures in multiple sclerosis patients, warranting further development of ADS-5102
- Initiated clinical development of ADS-4101, a potential once-daily, high-dose chrono-synchronous lacosamide therapy, for the treatment of partial onset seizures in patients with epilepsy; lacosamide is an anti-epilepsy active ingredient previously approved by the FDA and currently marketed as VIMPAT® (lacosamide)
- Completed a single-dose Phase 1 trial of four formulations of ADS-4101, and plan to present the data at a medical meeting in 2017
- Promoted Jennifer J. Rhodes to the position of Chief Business Officer in recognition of her contribution to Adamas and significant commercial experience in the pharmaceutical and biotech industry. She will continue to serve as General Counsel, Chief Compliance Officer, and Corporate Secretary
- Broadened the responsibilities of Rajiv Patni, M.D., Chief Medical Officer, to lead all Research and Development activities
- FDA approval of the NDA for ADS-5102 for the treatment of LID in patients with Parkinson’s disease
- Launch of ADS-5102 in the U.S. for the treatment of LID in patients with Parkinson’s disease, if approved, in the second half of 2017
- Evaluation of additional indications for ADS-5102 including Phase 3 development for the treatment of walking impairment in patients with multiple sclerosis and for the management of patients earlier in the Parkinson’s disease treatment journey
- Completion of Phase 1 clinical trials of ADS-4101 to select suitable formulations to advance into pivotal studies
- Presentation of clinical data at the American Academy of Neurology (AAN) Annual Meeting and other medical meetings throughout 2017
Fourth Quarter and Full-Year 2016 Financial Results
Adamas reported a net loss of $15.0 million, or $0.68 per share, basic and diluted, for the fourth quarter of 2016, compared to a net loss of $10.7 million, or $0.58 per share, basic and diluted, for the fourth quarter of 2015. For the year ended December 31, 2016, Adamas reported a net loss of $60.1 million, or $2.77 per share, basic and diluted, compared to a net loss of $51.8 million, or $2.86 per share, basic and diluted, for 2015.
For the quarter ended December 31, 2016, Adamas recorded revenues of $37,000 compared to $0.5 million in the corresponding period of 2015. Adamas recorded total revenues of $0.6 million for the full-year 2016, compared to $1.9 million during the same period of 2015. The decrease reflected the reduction in reimbursements for activities Adamas employees performed related to a license agreement with Allergan.
Research and development (R&D) expenses for the quarter ended December 31, 2016, were $7.0 million, including $0.7 million in stock-based compensation expense, compared to $9.7 million for the quarter ended December 31, 2015, which included $0.9 million in stock-based compensation expense. For the full-year 2016, R&D expenses were $31.2 million, including $2.9 million in stock-based compensation expense, compared to $35.9 million for the full-year 2015, which included $3.2 million in stock-based compensation expense. R&D expenses for the full-year declined over the prior period primarily due to the completion of Phase 3 clinical trials of ADS-5102 for LID in patients with Parkinson’s disease.
General and administrative (G&A) expenses for the quarter ended December 31, 2016, were $8.3 million, including $2.1 million in stock-based compensation expense, compared to $6.9 million for the same quarter in the prior year, which included $1.9 million in stock-based compensation expense. In the full-year 2016, G&A expenses were $30.3 million, including $7.7 million in stock-based compensation expense, compared to $23.5 million, including $6.8 million in stock-based compensation expense, incurred during the full-year 2015. The increase in G&A expenses for the fourth quarter and full-year was primarily due to increased investment in infrastructure to support the anticipated commercialization of ADS-5102 for LID in Parkinson’s disease.
On December 31, 2016, Adamas had $135.9 million of cash, cash equivalents and available-for-sale securities compared to $120.0 million at December 31, 2015. On January 6, 2016, Adamas raised net proceeds of $61.8 million from the sale of 2,875,000 shares of common stock through a follow-on public offering.
About Adamas Pharmaceuticals, Inc.
Adamas develops new medicines to improve the daily lives of those affected by chronic neurologic disorders, including Parkinson’s disease, multiple sclerosis, epilepsy and Alzheimer’s disease. Adamas has pioneered a platform to develop medicines, called chrono-synchronous therapies, for chronic neurologic disorders based on an understanding of the time-dependent biologic processes responsible for disease activity and drug response to potentially achieve symptomatic relief without tolerability issues. The company’s most advanced product candidate, ADS-5102, is in development for levodopa-induced dyskinesia (LID) in patients with Parkinson’s disease and walking impairment. An NDA supporting ADS-5102 for the treatment of LID in patients with Parkinson’s disease is under review by the FDA, with a PDUFA date of August 24, 2017. Adamas is exploring other indications for ADS-5102 for further development. Adamas is also investigating ADS-4101 for the treatment of partial onset seizures in patients with epilepsy. Additionally, Adamas’ licensed assets, NAMENDA XR® and NAMZARIC®, are currently marketed by Allergan, and Adamas is eligible to receive royalties on sales of these medicines beginning in June 2018 and May 2020, respectively. For more information, please visit www.adamaspharma.com.
VIMPAT® is a trademark of UCB. Namenda XR® and Namzaric® are trademarks of Merz Pharma GmbH & Co. KGaA.
Statements contained in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including but not limited to, statements contained in this press release regarding the potential approval and commercial launch of ADS-5102 for treatment of levodopa-induced dyskinesia in patients with Parkinson’s disease, the potential for additional clinical development programs for ADS-5102 including walking impairment in multiple sclerosis and other indications, that 2017 will be a pivotal year as Adamas transforms from an R&D-focused company to a commercial organization, the advancement of ADS-4101 in clinical development, and the statements under the heading “Anticipated Milestones.” Words such as “expect,” “anticipate,” and similar expressions (as well as other words or expressions referencing future events, conditions, or circumstances) are intended to identify forward-looking statements. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. For a description of risks and uncertainties that could cause actual results to differ from those expressed in forward-looking statements, including risks relating to Adamas’ research, clinical, development and commercial activities relating to ADS-5102 and ADS-4101, the regulatory and competitive environment and Adamas’ business in general, see Adamas’ Annual Report on Form 10-K filed with the Securities and Exchange Commission on February 28, 2017. Investors are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this release. Adamas undertakes no obligation to update any forward-looking statement in this press release.
— Financial Tables Attached —
|Adamas Pharmaceuticals, Inc.|
|Unaudited Consolidated Statements of Operations|
|(in thousands, except per share data)|
|Three Months Ended|
|Twelve Months Ended|
|Research and development||7,047||9,697||31,230||35,895|
|General and administrative, net||8,283||6,890||30,326||23,458|
|Total operating expenses||15,330||16,587||61,556||59,353|
|Loss from operations||(15,293||)||(16,063||)||(60,984||)||(57,437||)|
|Interest and other income, net||218||98||811||363|
|Loss before income taxes||(15,075||)||(15,965||)||(60,173||)||(57,074||)|
|Benefit for income taxes||(115||)||(5,275||)||(115||)||(5,272||)|
|Net loss per share, basic and diluted||$||(0.68||)||$||(0.58||)||$||(2.77||)||$||(2.86||)|
|Weighted average shares used in computing net loss|
per share, basic and diluted
|Adamas Pharmaceuticals, Inc.|
|Unaudited Consolidated Balance Sheets|
|(in thousands, except share and per share data)|
|Cash and cash equivalents||$||23,735||$||33,104|
|Prepaid expenses and other current assets||2,541||5,108|
|Total current assets||116,987||113,187|
|Property and equipment, net||3,156||2,353|
|Available-for-sale securities, non-current||22,292||13,165|
|Liabilities and stockholders’ equity|
|Other current liabilities||287||298|
|Total current liabilities||9,743||11,807|
|Commitments and Contingencies|
|Preferred stock, $0.001 par value — 5,000,000 shares authorized, and zero|
shares issued and outstanding at December 31, 2016 and December 31, 2015
|Common stock, $0.001 par value — 100,000,000 shares authorized, 22,013,644|
and 18,505,462 shares issued and outstanding at December 31, 2016 and
December 31, 2015, respectively
|Additional paid-in capital||254,558||178,473|
|Accumulated other comprehensive loss||(193||)||(158||)|
|Total stockholders’ equity||132,183||116,187|
|Total liabilities and stockholders’ equity||$||142,473||$||128,743|
|Adamas Pharmaceuticals, Inc.|
|Unaudited Consolidated Statements of Cash Flows|
|Twelve Months Ended|
|Cash flows from operating activities|
|Adjustments to reconcile net loss to net cash used in operating activities|
|Net accretion of discounts and amortization of premiums of available-for-|
|Changes in assets and liabilities|
|Accrued interest of available-for-sale securities||(2||)||110|
|Prepaid expenses and other assets||2,643||(4,416||)|
|Accrued liabilities and other liabilities||(2,721||)||(820||)|
|Net cash used in operating activities||(48,068||)||(47,210||)|
|Cash flows from investing activities|
|Purchases of property and equipment||(1,624||)||(1,399||)|
|Purchases of available-for-sale securities||(103,528||)||(59,828||)|
|Maturities of available-for-sale securities||78,443||69,285|
|Net cash provided by (used in) investing activities||(26,709||)||8,058|
|Cash flows from financing activities|
|Proceeds from public offerings, net of offering costs||61,822||9,657|
|Proceeds from issuance of common stock upon exercise of stock options||2,966||746|
|Proceeds from employee stock purchase plan||620||407|
|Net cash provided by financing activities||65,408||10,810|
|Net decrease in cash and cash equivalents||(9,369||)||(28,342||)|
|Cash and cash equivalents at beginning of period||33,104||61,446|
|Cash and cash equivalents at end of period||$||23,735||$||33,104|
Contact: Martin Forrest Vice President, Corporate Communications & Investor Relations Adamas Pharmaceuticals, Inc. 510-450-3528 firstname.lastname@example.org
Source:Adamas Pharmaceuticals, Inc.