Inbrija is administered by inhalation and is indicated for the intermittent treatment of off episodes in patients with Parkinson's disease currently taking carbidopa/levodopa. Inbrija is approved by the FDA and the EU.
In September 2014, the company acquired Civitas Therapeutics for, gaining the Phase III Parkinson’s drug, CVT-301, the migraine drug CVT-427 and rights to the ARCUS pulmonary delivery system. Th ARCUS technology allows for the administration of drugs by inhalation. The FDA-approved drug Inbrija and the clinical-stage drug CVT-427 currently use the ARCUS technology for drug delivery.
Acorda Therapeutics was incorporated in 1995, founded by internist turned entrepreneur Ron Cohen in Hawthorne, New York. Cohen had previously worked at the tissue engineering firm Advanced Tissue Sciences from 1986 to 1992. Cohen's focus on neurology at Acorda was influenced by his father's being a neurologist at Columbia University Medical Center. The business model of the company from the start was to work on commercialization of academic discoveries. A single therapeutic area focus also has the advantage that physicians prescribing one drug might also prescribe another in Acorda's portfolio; for instance, the company planned to leverage physician access through tizanidinecapsule sales to promote dalfampridine sales. An initial public offering in 2006 raised, about half of what was expected going into the offering, which was attributed to general weakness of the IPO market at the time. These funds were supplemented by a private sale of shares later the same year, raising and additional. As of 2007, twelve years after incorporation, the company had not yet turned a profit.
Dalfampridine
The Canadian Spinal Research Organization held the patent for this drug in 2002 when the organization engaged Acorda to conduct a Phase III trial for treatment of spasticity in patients with chronic spinal cord injury. This was Acorda's flagship product and development of subsequent drug candidates was initially predicated on realized revenue from this drug's sales. In November 2016, the company announced it was discontinuing development of the drug for post-stroke walking difficulties, after a clinical trial failure. In the third quarter of 2019, the company's shares dropped by a significant 65.1% as a result of dalfampridine's multiple sclerosis indication facing competition in the United States.
Inbrija
In December 2018, the company announced the FDA approval of Inbrija for patients with Parkinson's disease.
Tizanidine
The company licensed tizanidine from Élan in the early 2000s to help meeting cash flow goals. Acorda sells both capsule and tablet forms of this drug, with emphasis on the capsule form as this has patent protection through 2021, while the tablet form has many generic competitors.
, the members of the board of directors of Acorda Therapeutics were: Ron Cohen, Barry Greene, Peder K. Jensen, John P. Kelley, Sandra Panem, Lorin J. Randall, Steven M. Rauscher, and Catherine D. Strader. , the members of the senior management team were: Ron Cohen M.D., Burkhard Blank, Andrew R. Blight, Denise Duca, Andrew A. Hidman, David Lawrence, Lauren Sabella, Tierney Saccavino and Jane Wasman. , founder, President and CEO Cohen would be about 63 years old. Andrew Blight was the CSO in 2007 and be about 68 years old, an emeritus in this role. As of 2007, David Lawrence was the Chief Financial Officer and Mary Fisher the Chief Operating Officer. Jane Wasman, about 62 in 2019, has held the General Counsel role at the company since at least 2007.
