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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

U S FDA Accepts Biologics License Application for GC Biopharma s GC5107B (Immune Globulin Intravenous (Human), 10% Liquid)

/PRNewswire/ GC Biopharma (006280.KS), a global biopharmaceutical company dedicated to specialty plasma-derived therapeutics, today announced that the U.S..

South koreaUnited statesSohee kimYelin junMarketing research bureauDrug administrationGreen cross corporationBiologics license applicationImmune globulin intravenousPrescription drug user fee actPrimary immunodeficiencyPrimary immunodeficiency diseasesAnn allergy clin immunolGc biopharma

Grifols Achieves Positive Topline Results From Phase 4 Study of XEMBIFY® (immune globulin subcutaneous human-klhw) Evaluating Biweekly Dosing Option for Patients

Grifols Achieves Positive Topline Results From Phase 4 Study of XEMBIFY® (immune globulin subcutaneous human-klhw) Evaluating Biweekly Dosing Option for Patients
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United statesComunidad autonoma de catalunaKim hannaClinical developmentInvestors relations department sustainabilityDrug administrationMarketing research bureauMedia press officetelSpanish stock exchangeUnited states foodGrifols senior director clinicalImmune globulinChromatography purifiedPrescribing informationNorth americaMiddle east

Grifols Achieves Positive Topline Results From Phase 4

Clinical trial met primary endpoint demonstrating comparable total immunoglobulin (Ig) levels when administering XEMBIFY® (Grifols’ subcutaneous Ig) every.

United statesComunidad autonoma de catalunaKim hannaMarketing research bureauSpanish stock exchangeClinical developmentDrug administrationInvestors relations department sustainabilityMedia press officeUnited states foodGrifols senior director clinicalImmune globulinChromatography purifiedPrescribing informationNorth americaMiddle east