Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
FDA Accepts BLA Re-Submission for Takeda’s Entyvio SC
Takeda Pharmaceutical said on April 27 that the US FDA has accepted for review its re-submission for a subcutaneous (SC) formulation of Takeda Pharmaceutical’s inflammatory bowel disease drug Entyvio (vedolizumab). The company expects a decision before the end of the…
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