Brief: U.S. FDA Accepts Takeda's Application For Intravenous Entyvio® (Vedolizumab) In Pediatric Ulcerative Colitis And Crohn's Disease
BRIEF-U.S. FDA Accepts Takeda's Application For Intravenous Entyvio® (Vedolizumab) In Pediatric Ulcerative Colitis And Crohn's Disease June 9 (Reuters) - Takeda Pharmaceutical Co Ltd 4502.T:
U.S. FDA ACCEPTS TAKEDA'S APPLICATION FOR INTRAVENOUS ENTYVIO® (VEDOLIZUMAB) IN PEDIATRIC ULCERATIVE COLITIS AND CROHN'S DISEASE
TAKEDA PHARMACEUTICAL CO - FDA SETS PDUFA GOAL DATE IN Q1 2027 FOR ENTYVIO APPLICATION
Source text: ID:nBwb9nn9a
Further company coverage: 4502.T
((Reuters.Briefs@thomsonreuters.com;))
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Brief: U.S. FDA Accepts Takeda's Application For Intravenous Entyvio® (Vedolizumab) In Pediatric Ulcerative Colitis And Crohn's Disease
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