Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
US Sunovion to Resubmit NDA for Antiepileptic Treatment STEDESA
Dainippon Sumitomo Pharma Co., Ltd. announced on December 5 that its US subsidiary Sunovion Pharmaceuticals Inc., currently applying for U.S. Food and Drug Administration (FDA) approval for its antiepileptic drug STEDESA (eslicarbazepine acetate), had finalized its plans to resubmit a…
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