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Takeda Receives Positive CHMP Opinion for Recombinant ADAMTS13 rADAMTS13 in Congenital Thrombotic Thrombocytopenic Purpura cTTP

Takeda TSE4502NYSETAK today announced that the European Medicines Agencys EMA Committee for Medicinal Products for Human Use CHMP has recommended the approval under exceptional circumstances of recombinant ADAMTS13 rADAMTS13 for the treatment of ADAMTS13 deficiency in children and adult patients with cTTP.

United statesKremer hovingaJun saitoVan dorlandThromb haemostTakeda pharmaceutical company limitedExchange commissionJapanese ministry of healthEuropean medicines agencyEuropean commissionTreatment optionsDrug administrationEuropean unionFranchise global program leader at takedaCommittee for medicinal products human usePotentially fatal blood clotting disorder

Takeda Receives Positive CHMP Opinion for Recombinant ADAMTS13 (rADAMTS13) in Congenital Thrombotic Thrombocytopenic Purpura (cTTP)

Takeda Receives Positive CHMP Opinion for Recombinant ADAMTS13 (rADAMTS13) in Congenital Thrombotic Thrombocytopenic Purpura (cTTP)
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United statesKremer hovingaVan dorlandThromb haemostFranchise global program leader at takedaJapanese ministry of healthEuropean unionTakeda pharmaceutical company limitedDrug administrationEuropean commissionExchange commissionEuropean medicines agencyCommittee for medicinal products human useMedicinal productsHuman useObi umeh

Takeda Pharmaceutical Company Limited: Takeda Receives Positive CHMP Opinion for Recombinant ADAMTS13 (rADAMTS13) in Congenital Thrombotic Thrombocytopenic Purpura (cTTP)

Takeda Pharmaceutical Company Limited: Takeda Receives Positive CHMP Opinion for Recombinant ADAMTS13 (rADAMTS13) in Congenital Thrombotic Thrombocytopenic Purpura (cTTP)
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United statesNordrhein westfalenMark doleKremer hovingaJun saitoVan dorlandThromb haemostExchange commissionDrug administrationEuropean commissionCommittee for medicinal products human useFranchise global program leader at takedaJapanese ministry of healthEuropean medicines agencyTakeda pharmaceutical company limitedInternational media

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

Oxford byelection called, and divided Tories can t afford to lose it: Expert

Oxford byelection called, and divided Tories can t afford to lose it: Expert
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