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Atamyo Therapeutics Obtains Regulatory Authorization in Europe to Initiate a Clinical Trial for ATA-200, its Gene Therapy to Treat Limb-Girdle Muscular Dystrophy Type 2C/R5

Atamyo Therapeutics Obtains Regulatory Authorization in Europe to Initiate a Clinical Trial for ATA-200, its Gene Therapy to Treat Limb-Girdle Muscular Dystrophy Type 2C/R5
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Sophie olivierDennis riedlCharles craigIsabelle richardItalian medicines agencyOpus biotech communicationsUniversity of milanProgressive muscular dystrophies laboratory at genethonFrench medicines agencyEuropean medicines agencyNational centerScientific researchClinical trial applicationChief medical officerGiacomo comiFull professor

Gene therapy for rare muscular dystrophy presents promise

Gene therapy for rare muscular dystrophy presents promise
europeanpharmaceuticalreview.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from europeanpharmaceuticalreview.com Daily Mail and Mail on Sunday newspapers.

United kingdomJohn vissingSophie olivierInternational limbDrug administrationEuropean society of gene cell therapyAtamyo therapeuticsEuropean societyCell therapyLimb girdle muscular dystrophyChief medicalData safety monitoring boardInvestigational new drug

Atamyo Therapeutics: First Clinical Results of ATA-100, a Gene Therapy for the Treatment of Limb-Girdle Muscular Dystrophy Type 2I/R9 (LGMD2I/R9), Presented at ESGCT

Atamyo Therapeutics: First Clinical Results of ATA-100, a Gene Therapy for the Treatment of Limb-Girdle Muscular Dystrophy Type 2I/R9 (LGMD2I/R9), Presented at ESGCT
finanznachrichten.de - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from finanznachrichten.de Daily Mail and Mail on Sunday newspapers.

United kingdomUnited statesBruxelles capitaleJohn vissingIsabelle richardIndiens wirtschaftSophie olivierCharles craigNicolai preislerIhre chancenOpus biotech communicationsProgressive muscular dystrophies laboratory at genethonInternational limbEuropean society of gene cell therapyData safety monitoring boardAnnual congress

First Clinical Results of ATA-100, a Gene Therapy for the Treatment of Limb-Girdle Muscular Dystrophy Type 2I/R9 (LGMD2I/R9), Presented at ESGCT

First Clinical Results of ATA-100, a Gene Therapy for the Treatment of Limb-Girdle Muscular Dystrophy Type 2I/R9 (LGMD2I/R9), Presented at ESGCT
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United statesUnited kingdomBruxelles capitaleIsabelle richardCharles craigNicolai preislerJohn vissingSophie olivierEuropean society of gene cell therapyOpus biotech communicationsProgressive muscular dystrophies laboratory at genethonInternational limbData safety monitoring boardAnnual congressEuropean societyCell therapy

ATA-200, Atamyo Therapeutics Gene Therapy to Treat Limb-Girdle Muscular Dystrophy Type 2C/R5, Reaches Key Milestones with the Filing of a Clinical Trial Application in Europe and a Non-Dilutive Financing from France 2030 Program

ATA-200, Atamyo Therapeutics Gene Therapy to Treat Limb-Girdle Muscular Dystrophy Type 2C/R5, Reaches Key Milestones with the Filing of a Clinical Trial Application in Europe and a Non-Dilutive Financing from France 2030 Program
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Baden wübergCharles craigIsabelle richardSophie olivierStephane degoveOpus biotech communicationsProgressive muscular dystrophies laboratory at genethonClinical trial applicationAdeno associated virusChief medical officerChief scientific officerEuropean clinicalChief executive officerProgressive muscular dystrophies laboratoryCeltic ataoFrance republic