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

U.S. FDA Approves Subcutaneous Administration of Takeda's ENTYVIO® (vedolizumab) for Maintenance Therapy in Moderately to Severely Active Crohn's Disease
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United statesAbhyankarbj crohnsLe berreTimothy ritterGi alliance researchTakeda pharmaceutical company limitedTakeda pharmaceuticals united statesa incDrug administrationTakeda pharmaceuticalsExchange commissionSchool of medicineEuropean unionDepartment of researchDisease activity indexHypersensitivity reactionsMultifocal leukoencephalopathy

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

U.S. FDA Approves Subcutaneous Administration of Takeda's ENTYVIO® (vedolizumab) for Maintenance Therapy in Moderately to Severely Active Crohn's Disease
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United statesAmy mccarthyJun saitoTimothy ritterAbhyankarbj crohnsLe berreDepartment of researchSubcutaneous administration of takedaEuropean unionTakeda pharmaceuticalsGi alliance researchTakeda pharmaceutical company limitedInternational mediaDrug administrationExchange commissionSchool of medicine

Takeda Announces Approval of ADZYNMA® Intravenous Injection 1500 (apadamtase alfa /cinaxadamtase alfa) in Japan for Patients with Congenital Thrombotic Thrombocytopenic Purpura (cTTP)

cTTP is an Ultra-rare Blood Clotting Disorder Associated with Life-Threatening Acute Events and Debilitating Chronic Symptoms ADZYNMA is the First and Only Recombinant ADAMTS13 Enzyme.

United statesYasushi kajiiThromb haemostKremer hovingaVan dorlandEuropean medicines agencyJapan ministry of healthTakeda pharmaceutical company limitedExchange commissionDrug administrationJapanese ministry of healthTakeda pharmaceuticals united statesa incJapanese ministryOrphan drug designationProduct overviewSpecific populations

Takeda and Protagonist Therapeutics, Inc. Enter into Worldwide License and Collaboration Agreement for Rusfertide, a Late-Stage Rare Hematology Asset

Takeda and Protagonist Therapeutics, Inc. Enter into Worldwide License and Collaboration Agreement for Rusfertide, a Late-Stage Rare Hematology Asset
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United kingdomUnited statesDineshv patelAnn hematolJulie kimUs coJapan ministry of healthEuropean medicines agencyTakeda pharmaceutical company limitedDrug administrationTakeda pharmaceuticals united statesa incExchange commissionProtagonist therapeutics incAmerican society of hematologyBe protagonist coTakeda will be protagonist

Takeda and Protagonist Therapeutics, Inc. Enter into Worldwide License and Collaboration Agreement f

Takeda Will Be Protagonist's Co-Development, U.S. Co-Commercialization Partner With 50:50 Profit Share, and With Exclusive Ex-U.S. Global Rights to Commercialize Rusfertide, Protagonist's Investigational Injectable Hepcidin Mimetic Currently in Development for the Treatment of Polycythemia Vera (PV)Takeda Will Make.

United statesUnited kingdomAnn hematolDineshv patelJulie kimBe protagonist coTakeda pharmaceutical company limitedDrug administrationExchange commissionTakeda pharmaceuticals united statesa incEuropean medicines agencyProtagonist therapeutics incAmerican society of hematologyJapan ministry of healthUs coTakeda will be protagonist