Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
DSP’s US Subsidiary Sunovion Announces FDA Acceptance of NDA Resubmission for Epilepsy Treatment Stedesa
Dainippon Sumitomo Pharma’s US subsidiary Sunovion Pharmaceuticals announced on February 27 (US time) that the US FDA has accepted the company’s new drug application (NDA) resubmission for Stedesa (eslicarbazepine acetate) for use in patients with epilepsy. Sunovion submitted the original…
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