Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
FDA Nixes Sunovion’s Parkinson’s Drug, but Requires No New Studies
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…
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