FDA Reviewing Request to Approve ADS-5102 to Treat Levodopa-induced Dyskinesia
The U.S. Food and Drug Administration (FDA) has agreed to review a request by Adamas Pharmaceuticals to approve ADS-5102 (amantadine hydrochloride) extended-release capsules to treat levodopa-induced dyskinesia (LID) in patients with Parkinson’s disease (PD). The company submitted the request as New Drug Application (NDA) to the FDA in October. A…