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Takeda Pharmaceutical (TAK) Presents Full Data Set from Phase 3 ADVANCE-CIDP 1 Trial of HYQVIA

Takeda Pharmaceutical (TAK) Presents Full Data Set from Phase 3 ADVANCE-CIDP 1 Trial of HYQVIA
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United statesCity ofUnited kingdomKristina allikmetsRobert haddenLauren padovanClinical programTakeda pharmaceutical company limitedEuropean medicines agencyKing college hospitalPeripheral nerve societyInternational mediaExchange commissionTakeda pharmaceutical companyResearch development for takeda plasmaEuropean union

Addentax Group Corp (ATXG) in Advanced Talks to Acquire Partial Stake in RMB 6B Recombinant Protein Drugs

Addentax Group Corp (ATXG) in Advanced Talks to Acquire Partial Stake in RMB 6B Recombinant Protein Drugs
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New zealandSherry zhengZhida hongBao pharmaHong zhidaCompany contactShanghai bao pharmaceutical company limited pharmaShenzhen oriental fortune capital co ltdShenzhen grandway capital management co ltdShanghai sun rock capital management co ltdWeitian groupCenter laboratories incHaitong innovation private fund management co ltdAddentax group corpCompany nasdaqDevices safety authority

Addentax Group Corp in Advanced Talks to Acquire Partial Stake in RMB 6 Billion-Valued Recombinant Protein Drugs and Antibody Drugs Bio-pharmaceutical Company, Shanghai Bao Pharmaceutical Company Limited

Addentax Group Corp in Advanced Talks to Acquire Partial Stake in RMB 6 Billion-Valued Recombinant Protein Drugs and Antibody Drugs Bio-pharmaceutical Company, Shanghai Bao Pharmaceutical Company Limited
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New zealandBao pharmaSherry zhengHong zhidaZhida hongDevices safety authorityShanghai bao pharmaceutical companyHaitong innovation private fund management co ltdCenter laboratories incShanghai bao pharmaceutical company limited pharmaChina national medical products administrationWeitian groupAddentax group corpCompany nasdaqShenzhen grandway capital management co ltdAntibody drugs company

Takeda Pharmaceutical Co Ltd (TAK) Receives FDA Approval to Expand the Use of HYQVIA

Takeda Pharmaceutical Co Ltd (TAK) Receives FDA Approval to Expand the Use of HYQVIA
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United statesKasandra carrKate niaziExchange commissionTakeda pharmaceutical companyEuropean unionInternational mediaDeficiency foundationDrug administrationTakeda pharmaceutical company limitedWall streetJorey berryImmune deficiencyRecombinant human hyaluronidaseMeningitis syndromeLocalized infection

Takeda Receives FDA Approval to Expand the Use of HYQVIA® to Treat Primary Immunodeficiency in Children

HYQVIA® [Immune Globulin Infusion 10% with Recombinant Human Hyaluronidase], the Only Once-a-Month – Every Three or Four Weeks – Subcutaneous Immunoglobulin , is Now Approved for. | April 11, 2023

United statesEuropean unionDeficiency foundationDrug administrationTakeda pharmaceutical company limitedExchange commissionJorey berryImmune deficiencyRecombinant human hyaluronidaseMeningitis syndromeLocalized infectionRelated acute lung injuryInfectious agentsLab testsRare geneticsPlasma derived therapies