Acorda reports $0.7 million GAAP net loss for first quarter 2011

Acorda Therapeutics, Inc. (Nasdaq: ACOR) today announced its financial results for the first quarter ended March 31, 2011.

“We also recently launched several initiatives highlighting the broad range of MS patients who can potentially benefit from AMPRYA, including those at earlier stages of their walking disability. We expect these programs will drive an increase in new patients being prescribed AMPYRA.”

"We were delighted that the U.S. Patent and Trademark Office allowed our patent application related to the use of sustained release 4-aminopyridine to improve walking in people with MS. This provides patent coverage into 2026 and significant additional runway for AMPYRA's life cycle management," said Ron Cohen, M.D., Acorda Therapeutics' President and CEO. "We also recently launched several initiatives highlighting the broad range of MS patients who can potentially benefit from AMPRYA, including those at earlier stages of their walking disability. We expect these programs will drive an increase in new patients being prescribed AMPYRA."

FINANCIAL RESULTS

The Company reported GAAP net loss of $0.7 million for the quarter ended March 31, 2011, or $0.02 per basic and diluted EPS, including share-based compensation charges totaling $3.8 million. The GAAP net loss for the first quarter of 2010 was $21.1 million, or $0.56 per basic and diluted EPS including share-based compensation charges of $3.2 million.

Non-GAAP net income, before share-based compensation charges, for the quarter ended March 31, 2011 was $3.1 million or $0.08 per share, compared to a non-GAAP net loss of $17.9 million, or $0.47 per share for the same quarter in 2010.

AMPYRA^® (dalfampridine) Extended Release Tablets, 10 mg net revenue - For the quarter ended March 31, 2011, the Company reported AMPYRA net revenue of $46.8 million, compared to $3.1 million in net revenue for the same quarter in 2010. Acorda began shipping AMPYRA to specialty pharmacies on March 1, 2010. AMPYRA revenue is recognized following shipment of the product from the Company's distribution facility to its network of specialty pharmacies.

ZANAFLEX CAPSULES^® (tizanidine hydrochloride) and ZANAFLEX^® (tizanidine hydrochloride) tablets net revenue - For the quarter ended March 31, 2011, the Company reported combined net revenue of ZANAFLEX CAPSULES and ZANAFLEX tablets of $12.2 million, compared to combined net revenue of $12.3 million for the same quarter in 2010.

ZANAFLEX revenue is recognized using a deferred revenue recognition model, meaning ZANAFLEX CAPSULES and ZANAFLEX tablets shipments to wholesalers are recorded as deferred revenue and only recognized as revenue when end-user prescriptions of ZANAFLEX CAPSULES and ZANAFLEX tablets are reported.

ZANAFLEX CAPSULES and ZANAFLEX tablets shipments - Total ZANAFLEX CAPSULES and ZANAFLEX tablets shipments for the quarter ended March 31, 2011 were $16.9 million, compared to total shipments of $13.4 million for the same quarter in 2010.

Research and development expenses for the quarter ended March 31, 2011 were $10.7 million, including $1.1 million of share-based compensation, compared to $8.1 million including $0.8 million of share-based compensation for the same quarter in 2010. Research and development expenses for the quarter included costs related to AMPYRA post-marketing studies and life cycle management programs, clinical costs associated with the close-out of the Company's AMPYRA multiple sclerosis (MS) extension study sites and the development of the Company's pipeline products, including Phase 1 clinical trial expenses for Glial Growth Factor 2 (GGF2).

The Company reaffirms its full year 2011 research and development expense guidance of $40-$45 million excluding share-based compensation charges.

Sales, general and administrative expenses for the quarter ended March 31, 2011 were $38.1 million, including $2.7 million of share-based compensation, compared to $26.7 million including $2.4 million of share-based compensation for the same quarter in 2010. The increase in expenses was primarily due to increases in AMPYRA sales and marketing activities and expenses related to ZANAFLEX CAPSULES patent infringement litigation.

The Company reaffirms its full year 2011 sales, general and administrative expense guidance of $130-$140 million excluding share-based compensation charges.

As of March 31, 2011, Acorda held cash, cash equivalents and short-term investments of $225.3 million.

This press release includes financial results prepared in accordance with accounting principles generally accepted in the United States (GAAP), and also certain historical and forward-looking non-GAAP financial measures. In particular, Acorda has provided its first quarter 2011 and 2010 income (loss), adjusted to exclude share-based compensation charges, and has also provided projected amounts of research and development (R&D) and sales, general, and administrative (SG&A) expenses excluding share-based compensation charges. These non-GAAP financial measures are not an alternative for financial measures prepared in accordance with GAAP. However, we believe the presentation of income (loss) and projected R&D and SG&A expenses excluding share-based compensation charges, when viewed in conjunction with our GAAP results, provide investors with a more meaningful understanding of our ongoing and projected operating performance because they exclude non-cash charges that are substantially dependent on changes in the market price of our common stock. We believe these non-GAAP financial measures help indicate underlying trends in the company's business, and are important in comparing current results with prior period results and understanding projected operating performance. Also, management uses these non-GAAP financial measures to establish budgets and operational goals, and to manage the company's business and to evaluate its performance. A reconciliation of the historical non-GAAP financial results presented in this release to our GAAP financial results is included in the attached financial statements.

AMPYRA UPDATE

• On April 19, the Company announced that the United States Patent and Trademark Office (USPTO) allowed U.S. Patent Application No. 11/010,828 entitled "Sustained Release Aminopyridine Composition." The claims of the patent application relate to methods to improve walking in patients with multiple sclerosis (MS) by administering 10 mg of sustained release 4-aminopyridine (dalfampridine) twice daily. The patent that issues from this application, which will be eligible for listing in the U.S. Food and Drug Administration (FDA) Orange Book, is set to expire in early February 2026, based on the USPTO's calculated patent term adjustment of 413 days, which the Company is currently evaluating.
• As part of the process to determine if AMPYRA is eligible for patent extension of up to five years under provisions in the Hatch-Waxman Act, the FDA issued notice that it had determined the total review period for AMPYRA. This finding is subject to a public comment period, during which a petition can be filed to recalculate the eligible days of review. Following the conclusion of this process, the FDA determination becomes final, and the patent term extension application is returned to the USPTO for review.
• New clinical data analyses on AMPYRA were presented at the American Academy of Neurology (AAN) meeting in April 2011. Data presentations included analyses showing that people with MS who responded to AMPYRA had comparable improvements in their walking regardless of baseline walking speed or overall level of MS-related disability. In addition, AMPYRA responders, regardless of baseline disability, showed clinically meaningful improvement on the 12-Item MS Walking Scale (MSWS-12), a patient-based questionnaire that measures the impact of MS on the patient's reported ability to perform daily activities related to walking.
• Effective March 4, 2011, the Company implemented a 7.5% increase for the wholesale acquisition price (WAC) of AMPYRA. The current WAC is $1,135.37 per 30-day supply (60-count pill bottle).
• Acorda is working closely with its partner Biogen Idec on an appeal of the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) negative opinion recommending against the approval of FAMPYRA (the proposed trade name for AMPYRA in Europe).

ZANAFLEX CAPSULES

• The litigation against Apotex Inc. in connection with its application for approval of a generic version of ZANAFLEX CAPSULES is proceeding. The trial date, initially set for April 25, has been moved to May 9, 2011.

PIPELINE

• The Phase 1 GGF2 clinical trial in heart failure patients, being conducted in collaboration with the Vanderbilt University Heart and Vascular Institute, is ongoing.

CORPORATE UPDATES

• Peder Jensen, M.D. was elected to the Board of Directors effective April 19, 2011. Dr. Jensen has more than 24 years of global drug development experience in both pharmaceutical and biotechnology companies, across therapeutic areas including neurology, cardiovascular, anti-infective, oncology and immunology. Most recently, he served as Corporate Senior Vice President, and General Manager, R&D for Japan and Asia/Pacific at Schering-Plough Corporation.
• Wise Young, Ph.D., M.D., resigned from the Board of Directors effective April 19, 2011. Dr. Young served on Acorda's Board of Directors since the Company's founding in 1995, and will continue to advise the Company in a consulting role as Special Scientific Advisor.