Japan’s drug pricing panel held its final round of industry hearings on December 10 as it heads toward the FY2026…
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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