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United kingdomSouth koreaNew zealandGreat britainJack coxLibby holmanDrug administrationBiogen incEisai europe ltdCommunications departmentEisai incWashington university school of medicineNational institutes of healthPublic relations departmentAlzheimer association international conferenceNational institute on

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Noord hollandUnited kingdomNew zealandUnited statesLibby holmanMichael irizarryDrug developmentEisai co ltdBrain healthCommunications departmentEisai coClinical researchAssociation international conferenceAlzheimer disease imaging consortiumPublic relations departmentAlzheimer association international conference

Eisai to Present the Latest Alzheimer s Disease Pipeline and Research

Eisai to Present the Latest Alzheimer s Disease Pipeline and Research
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Noord hollandUnited kingdomNew zealandUnited statesLibby holmanMichael irizarryEisai europe ltdEisai incAlzheimer association international conferencePublic relations departmentAlzheimer disease imaging consortiumAssociation international conferenceClinical researchEisai coBrain healthCommunications department

Biogen Inc (NASDAQ:BIIB) Q1 2023 Earnings Call Transcript

Operator: Good morning. My name is Bettina and I will be your conference operator today.

District of columbiaUnited statesMichael mcdonnellAdam keeneyMike mcdonnellChristopher viehbacherChuck trianoChris viehbacherGeoff meachamPaul matteisPhil nadeauPriya singhalSamsung bioepisHead of developmentBusiness developmentEuropean union

Eisai: Biologics License Application for Lecanemab Designated for Priority Review by China National Medical Products Administration

TOKYO, Feb 28, 2023 - (JCN Newswire) - Eisai Co., Ltd. and Biogen Inc. announced today that the Biologics License Application (BLA) for lecanemab (brand name in the U.S.: LEQEMBI), an investigational anti-amyloid

Dennis riedlNatacha gassenbachMinistry of healthDrug administrationBiogen incEisai co ltdPublic relations departmentNational medical products administrationEuropean medicines agencyDevices agencyBiologics license applicationPriority reviewApproval procedureNew england journalNew windowMedical devices agency