FDA Nixes Sunovion’s Parkinson’s Drug, but Requires No New Studies

February 1, 2019
US regulators have rebuffed Sunovion Pharmaceuticals’ APL-130277, a sublingual film form of apomorphine for the treatment of Parkinson’s disease, the company said on January 30. Sunovion, a US subsidiary of Sumitomo Dainippon Pharma, has received the FDA’s complete response letter...read more