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AC Immune and Takeda Sign Exclusive Option and License Agreement for Active Immunotherapy Targeting Amyloid Beta for Alzheimer s Disease | Region

AC Immune and Takeda Sign Exclusive Option and License Agreement for Active Immunotherapy Targeting Amyloid Beta for Alzheimer s Disease | Region
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United statesUnited kingdomSarah sheikhGary waandersChris stammCorey davisYuko yoneyamaAndrea pfeiferChris maggos cohesion bureauNational institute on aging alzheimer associationInvestor relations corporate communicationsInternational mediaTakeda pharmaceutical companyExchange commissionSecurities exchangeGlobal development at takeda

AC Immune and Takeda Sign Exclusive Option and License Agreement for Active Immunotherapy Targeting Amyloid Beta for Alzheimers Disease

AC Immune and Takeda Sign Exclusive Option and License Agreement for Active Immunotherapy Targeting Amyloid Beta for Alzheimers Disease
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United kingdomUnited statesGary waandersSarah sheikhCorey davisAndrea pfeiferYuko yoneyamaTakeda pharmaceutical company limitedExchange commissionInternational mediaChris maggos cohesion bureauSecurities exchangeInvestor relations corporate communicationsGlobal development at takedaNational institute on aging alzheimer associationNeuroscience therapeutic area unit

Takeda Announces Positive Topline Results from Phase 2 Study Evaluating Mezagitamab TAK079 a Potential BestinClass AntiCD38 Monoclonal Antibody for Primary Immune Thrombocytopenia

TakedaTSE4502NYSETAK today announced positive topline results from a Phase 2 randomized doubleblind placebocontrolled study evaluating the safety tolerability and efficacy of mezagitamab TAK079 in patients with persistent or chronic primary immune thrombocytopenia ITP.

United statesChinwe ukomaduYuko yoneyamaRodeghierof international journal of hematologyTakeda pharmaceutical company limitedExchange commissionDevelopment in fiscal yearDrug administrationEfficacy resultsMezagitamab safeTakeda intendsGlobal phasePrimary immune thrombocytopeniaFiscal yearLate stage pipeline continuesInflammation therapeutic area unit

Takeda Intends to Rapidly Initiate the First Global Phase 3 Trials of TAK-861, an Oral Orexin Agonist, in Narcolepsy Type 1 in First Half of Fiscal Year 2024

Takeda Intends to Rapidly Initiate the First Global Phase 3 Trials of TAK-861, an Oral Orexin Agonist, in Narcolepsy Type 1 in First Half of Fiscal Year 2024
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United statesNew yorkJoe oconnorYuko yoneyamaChris stammBarbara shecterGabriel friedmanExchange commissionUpcoming scientific congressBell canadaInternational mediaTakeda pharmaceutical company limitedNational postBusiness wireRapidly initiateFirst global phase

Takeda Intends to Rapidly Initiate the First Global Phase 3 Trials of TAK861 an Oral Orexin Agonist in Narcolepsy Type 1 in First Half of Fiscal Year 2024

Takeda TSE4502NYSETAK today announced positive topline results from a randomized doubleblind placebocontrolled multiple dose Phase 2b trial evaluating TAK861 an oral orexin receptor 2 OX2R agonist in patients with narcolepsy type 1.

United statesYuko yoneyamaTakeda pharmaceutical company limitedExchange commissionUpcoming scientific congressKey secondary endpoints were metNarcolepsy typeGenerally safeResults willUpcoming scientificWakefulness testAnnual reportMedia contactTakeda tak861 orexin receptor 2 ox2r narcolepsy type 1 nct05687903 nct05687916 nt1 nt2 maintenance of wakefulness test epworth sleepiness scale weekly cataplexy rate sarah sheikh gastrointestinal inflammation rare diseases plasmaderived therapies oncology neuroscience vaccines