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FDA approves Takeda s self-administered Entyvio for Crohn s disease

Takeda has announced that the U.S. Food and Drug Administration (FDA) has approved a subcutaneous (SC) version of Entyvio, its treatment for adults with moderate to severe Crohn’s disease (CD).

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Subcutaneous Vedolizumab Approved for Moderate-to-Severe Crohn Disease

Announced on April 18, the approval is based on the VISIBLE 2 trial and comes less than 7 months after the approval of SC vedolizumab in ulcerative colitis.

Timothy ritterDepartment of researchGi alliance researchUs gastroenterology business unit at takeda pharmaceuticalsDrug administrationSchool of medicineTakeda pharmaceuticalsBrandon monkBusiness unit

U S FDA Approves Subcutaneous Administration of Takeda s ENTYVIO (vedolizumab) for Maintenance Therapy in Moderately to Severely Active Crohn s Disease Seite 1

19.04.2024 - Takeda (TSE:4502/NYSE:TAK) today announced that the U.S. Food and Drug Administration (FDA) has approved ENTYVIO (vedolizumab) subcutaneous (SC) administration for maintenance therapy in adults with moderately to severely active Crohn’s disease (CD) . Seite 1

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Takeda s Entyvio snags second FDA approval as subcutaneous option for Crohn s disease

Takeda s Entyvio snags second FDA approval as subcutaneous option for Crohn s disease
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FDA OKs Sub-Q Vedolizumab for Crohn s Maintenance Therapy

Subcutaneous administration of vedolizumab is now approved for maintenance therapy in adults with moderate to severe active Crohn's disease after induction therapy with intravenous vedolizumab.

United statesBurnett schoolFort worthTimothy ritterDrug administrationGi alliance researchBurnett school of medicineEntyvio penDisease activity index