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Takeda Announces Approval of CUVITRU Subcutaneous Immunoglobulin in Japan for Patients with Agammaglobulinemia or Hypogammaglobulinemia

Takeda TSE4502NYSETAK today announced that the Japanese Ministry of Health Labour and Welfare has approved the use of CUVITRU Immune Globulin Subcutaneous Human 20 Solution in patients aged 2 years and older with agammaglobulinemia or hypogammaglobulinemia1.

United statesNaoyoshi hirotaKristina allikmetsJavier chinenLauren padovanKarens tuanoSneha sethExchange commissionInternational mediaMarketing research bureauTakeda pharmaceutical company limitedCompany commitment to reach patientsNational organization for rare disordersJapanese ministry of healthClinical studies conductedNorth america confirming

Takeda Announces Approval of CUVITRU™ Subcutaneous Immunoglobulin in Japan for Patients with Agammaglobulinemia or Hypogammaglobulinemia

Approval is Based on Clinical Studies Conducted in Japan, Europe and North America Confirming the Efficacy and Safety of CUVITRU [Immune Globulin Subcutaneous , 20% Solution] CUVITRU is.

United statesSneha sethNaoyoshi hirotaKarens tuanoJavier chinenKristina allikmetsTakeda pharmaceutical company limitedMarketing research bureauNational organization for rare disordersJapanese ministry of healthExchange commissionJapanese ministryNorth americaPlasma derived therapies business unitPlasma derived therapies businessPrimary immunodeficiency

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