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European Commission Approves New Formulation of Takeda’s Entyvio
The European Comission has approved a subcutaneous formulation of Takeda Pharamceuticals’ Entyvio (vedolizumab) for treatment of ulcerative colitis and Crohn's disease.
The approval was based on the results of a phase 3 trial of the formulation as a maintenance therapy in adult patients. The participants achieved clinical response at week six following two doses of the intravenous formulation.
Takeda said the new formulation will be available in both a pre-filled syringe and a pre-filled pen.
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