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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 Pharmaceutical (TAK) Announces Approval of CUVITRU Subcutaneous Immunoglobulin in Japan

Takeda Pharmaceutical (TAK) Announces Approval of CUVITRU Subcutaneous Immunoglobulin in Japan
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United statesKristina allikmetsNaoyoshi hirotaJapanese ministry of healthJapanese ministryNorth americaPlasma derived therapies business unitPlasma derived therapies business

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

Takeda s TAKHZYRO® (lanadelumab) Approved in Japan for Prophylaxis Against Acute Attacks of Hereditary Angioedema (HAE)

Press release content from Business Wire. The AP news staff was not involved in its creation.

United statesLinda calandraNaoyoshi hirotaRyoko matsumotoErin marie bealsEuropean union summary of product characteristicsMinistry of healthTakeda pharmaceutical companyExchange commissionEuropean unionTakeda pharmaceutical company limitedTakeda development centerHereditary angioedema long term prophylaxisOpen label extensionJapan specific phaseHereditary angioedema

Takeda submits New Drug Application for lanadelumab in Japan

Takeda submits New Drug Application for lanadelumab in Japan
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Naoyoshi hirotaR takeda pharmaceutical companyJapan ministry of healthJapanese pharmaceuticalsMinistry of healthDevices agencyTakeda development center japanNew drug applicationDiana polekhinaMedical devices agencyDevelopment center japanHereditary angioedema long term prophylaxisOpen label extensionMenu hoverSubchild level menu hoverChild level menu hover