Press Releases
Atamyo Therapeutics to Provide Corporate Overviews and Updates on Its Pipeline Progress at 6 Upcoming Conferences in the US and Europe
Evry, France (September 16, 2024) – Atamyo Therapeutics, a biotechnology company focused on the development of new-generation gene therapies targeting neuromuscular disease, today announced its participation in six upcoming conferences in the US and Europe […]
Read moreProfessor Isabelle Richard has received the Fifth Annual LGMD2i Pioneer Award from Cure LGMD2i Foundation and the Speak Foundation
This recognition is for Isabelle Richard’s groundbreaking research on LGMD. Isabelle Richard, Ph.D., is Research Director at National Center of Scientific Research (CNRS) in France and head of the Progressive Muscular Dystrophies Laboratory at Genethon. We are […]
Read moreThe Dion Foundation and Atamyo Therapeutics Announce a Partnership to Expand into the US Atamyo’s Clinical Trial of ATA-200 Gene Therapy to Treat Limb-Girdle Muscular Dystrophy Type 2C/R5
Evry, France and Boston, MA (September 4, 2024) – Atamyo Therapeutics and The Dion Foundation for Children with Rare Diseases, today announced a key partnership to expand into the US a first-in-human clinical trial of […]
Read moreLa Dion Foundation et Atamyo Therapeutics annoncent un partenariat pour étendre aux États-Unis l’essai clinique d’Atamyo sur la thérapie génique ATA-200 pour traiter la myopathie des ceintures LGMD-2C/R5
Evry, France et Boston, Etats-Unis (le 4 septembre 2024) – Atamyo Therapeutics et The Dion Foundation for Children with Rare Diseases, ont annoncé aujourd’hui un partenariat clé pour étendre aux États-Unis l’essai clinique d’Atamyo sur […]
Read moreAtamyo Therapeutics obtient la désignation Fast Track de la FDA américaine pour ATA-100, thérapie génique en essai clinique de phase 1/2 pour la dystrophie musculaire des ceintures de type R9 (LGMD-R9)
Evry, France (24 juin 2024) – Atamyo Therapeutics, société de biotechnologie de stade clinique spécialisée sur le développement de thérapies géniques de nouvelle génération ciblant les dystrophies musculaires et les cardiomyopathies, a annoncé aujourd’hui que […]
Read moreAtamyo Therapeutics Obtains US FDA Fast Track Designation for ATA-100, a Gene Therapy in Phase 1/2 Clinical Trials for Limb-Girdle Muscular Dystrophy Type R9 (LGMD-R9)
Evry, France (June 24, 2024) – Atamyo Therapeutics, a clinical-stage biotechnology company focused on the development of new-generation gene therapies targeting muscular dystrophies and cardiomyopathies, today announced the US Food and Drug Administration has awarded […]
Read moreAtamyo Therapeutics Announces Scientific Communications on its LGMD Programs and Participation in Conferences
Five upcoming communications on LGMD programs at Myology 2024 Congress CEO Stephane Degove to present corporate overview at BioEquity Europe 2024 Evry, France (April 22, 2024) – Atamyo Therapeutics, a clinical-stage biotechnology company focused on […]
Read moreAtamyo 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 has received approval to initiate a clinical trial of ATA-200 gene therapy in France and Italy ATA-200 is a single-injection gene therapy aimed to treat LGMD2C/R5 caused by mutations in the gamma–sarcoglycan gene The […]
Read morePremiers résultats cliniques d’ATA-100, une thérapie génique pour le traitement de la dystrophie musculaire des ceintures de type 2I/R9 (LGMD 2I/R9), présentés au congrès ESGCT
ATA-100 est en cours d’évaluation dans l’étude de phase 1b/2b « ATA-001-FKRP » Recrutement de la première cohorte de 3 patients complété Premiers résultats de la première cohorte présentés à l’ESGCT en présentation orale Tolérance […]
Read moreFirst clinical results of ATA-100, a Gene Therapy for the Treatment of Limb-Girdle Muscular Dystrophy Type 2I/R9 (LGMD2I/R9), presented at ESGCT
ATA-100 is being evaluated in a multi-center phase 1b/2b “ATA-001-FKRP” study Completion of enrollment of the first dose cohort of 3 patients First results of cohort one presented at ESGCT in oral presentation Good clinical […]
Read more