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FDA Approves New Takeda Drug Delivery Option
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FDA Approves New Takeda Drug Delivery Option

Takeda Pharmaceutical Company (TAK) has released an update.

The U.S. FDA has approved Takeda’s ENTYVIO (vedolizumab) for subcutaneous administration as a maintenance therapy for adults with moderately to severely active Crohn’s Disease, expanding its availability alongside the existing IV option. The approval is backed by the VISIBLE 2 clinical trial, which showed that nearly half of the patients achieved long-term clinical remission. This new form of administration offers patients the flexibility to self-administer their treatment at home or on the move.

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