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The European Commission Approves Label Update for TAKHZYRO® (lanadelumab), Expanding Its Use to a Broader Group of Paediatric Patients with Recurrent Attacks of Hereditary Angioedema (HAE)

/PRNewswire/ Takeda (TSE:4502/NYSE:TAK) today announced the European Commission has approved TAKHZYRO® (lanadelumab) for the routine prevention of recurrent. ....

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The European Commission Approves Label Update for TAKHZYRO® (lanadelumab), Expanding Its Use to a Broader Group of Paedi

- TAKHZYRO® is the First Routine Prevention Treatment of HAE Approved in the EU for Patients Under the Age. ....

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- TAKHZYRO® is the First Routine Prevention Treatment of HAE Approved in the EU for Patients Under the Age of Six. ....

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Takeda: The European Commission Approves Label Update for TAKHZYRO® (lanadelumab), Expanding Its Use to a Broader Group of Paediatric Patients with Recurrent Attacks of Hereditary Angioedema (HAE)

Takeda: The European Commission Approves Label Update for TAKHZYRO® (lanadelumab), Expanding Its Use to a Broader Group of Paediatric Patients with Recurrent Attacks of Hereditary Angioedema (HAE)
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The European Commission Approves Label Update for TAKHZYRO® (lanadelumab), Expanding Its Use to a Broader Group of Paedi

- TAKHZYRO® is the First Routine Prevention Treatment of HAE Approved in the EU for Patients Under the Age. ....

United States , United Kingdom , Didier Relin , Prnewswire Takeda , Takeda Pharmaceutical Company , Takeda Pharmaceutical Company Limited , European Commission Decision , Drug Administration , European Medicines Agency , European Commission , Head Of International Regulatory At Takeda , First Routine Prevention Treatment , Patients Under , New Preventative Treatment Option , Hereditary Angioedema , European Economic Area , Adolescent Study , Biologics License Application , International Regulatory , Commission Decision , Open Label Phase , Evaluate Safety , Prevention Against Acute Attacks , Pediatric Patients , About Takeda Pharmaceutical , Rare Genetics ,