In both iv and subcutaneous administrations for maintenance treatment of adults with moderately to severely active ulcerative colitis or crohn’s disease takeda ( tse:4502/nyse:tak ) today announced that the u.s Fda approves subcutaneous administration of takeda's entyvio® (vedolizumab) for maintenance therapy in moderately to severely active ulcerative colitis Food and drug administration (fda) has approved entyvio ® (vedolizumab) subcutaneous (sc) administration for maintenance therapy in adults.
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Entyvio® dosing and administration for iv infusion and subcutaneous injection
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Additionally, a biologics license application for an investigational sc administration of entyvio. Background vedolizumab (entyvio) is a humanized monoclonal antibody utilized for the treatment of crohn’s disease and ulcerative colitis in adult patients