Four years after its initial approval in moderate to severe Crohn’s disease, Japan’s Takeda Pharmaceutical (TYO: 4502) has finally submitted Entyvio (vedolizumab) for approval in its home country.
The drug was approved by the European Medicines Agency and the US Food and Drug Administration in this indication in 2014.
Earlier this month, Takeda got the green light from the Japanese regulator to market Entyvio as a therapy for ulcerative colitis (UC).
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