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Biogen Receives European Commission Approval for QALSODY® (tofersen), the First Therapy to Treat a Rare, Genetic Form of ALS

Biogen Receives European Commission Approval for QALSODY® (tofersen), the First Therapy to Treat a Rare, Genetic Form of ALS
marketscreener.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from marketscreener.com Daily Mail and Mail on Sunday newspapers.

United kingdomUnited statesRegion flamandeChuck trianoStephanie fradettePhilip van dammeJack coxNational institute of neurological disordersDrug administrationEuropean commissionEuropean organisation for professionalsEuropean medicines agencyIonis pharmaceuticals incEuropean unionExchange commissionBiogen inc

Biogen Inc : Biogen Receives European Commission Approval for QALSODY® (tofersen), the First Therapy to Treat a Rare, Genetic Form of ALS

Biogen Inc : Biogen Receives European Commission Approval for QALSODY® (tofersen), the First Therapy to Treat a Rare, Genetic Form of ALS
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United kingdomUnited statesRegion flamandePhilip van dammeStephanie fradetteChuck trianoJack coxEuropean medicines agencyIonis pharmaceuticals incEuropean academy of neurologyUniversity hospital leuvenNeuromuscular reference centerEuropean unionExchange commissionNational institute of neurological disordersDrug administration

Biogen Receives European Commission Approval for QALSODY® (tofersen), the First Therapy to Treat a Rare, Genetic Form of ALS

Biogen Receives European Commission Approval for QALSODY® (tofersen), the First Therapy to Treat a Rare, Genetic Form of ALS
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United kingdomUnited statesRegion flamandeChuck trianoPhilip van dammeJack coxStephanie fradetteEuropean academy of neurologyEuropean medicines agencyEuropean organisation for professionalsIonis pharmaceuticals incEuropean commissionDrug administrationEuropean unionUniversity hospital leuvenNational institute of neurological disorders

Biogen : LEQEMBI® (Lecanemab) Approved for the Treatment of Alzheimer s Disease in South Korea

TOKYO and CAMBRIDGE, Mass., May 27, 2024 - Eisai Co., Ltd. and Biogen Inc. announced today that the Ministry of Food and Drug Safety in South Korea has approved humanized.

South koreaUnited kingdomUnited statesHaruo naitoChuck trianoChristophera viehbacherTsujim protofibrilsJulie edelmanLinkedinand facebookJack coxNational institute of dementia koreanExchange commissionMinistry of foodEisai co ltdUnited nations sustainable development goals sdgsInvestor relations department

Biogen Bolsters Late-Stage Pipeline, Expands Immunology Portfolio with Agreement to Acquire Human Immunology Biosciences

Transaction to include felzartamab, a potential first-in-class therapeutic candidate with promise as a pipeline-in-a-product across a range of immune-mediated diseasesFelzartamab is an investigational.

Hong kongUnited statesOlmsted countyUnited kingdomChuck trianoJack coxTravis murdochPriya singhalMorgan warnersExchange commissionHead of development at biogenGoodwin procterBofa securities incDrug administrationCovington burlingHuman immunology biosciences inc