Gene therapy
News
September 15, 2023
Genethon assesses a therapeutic potential of a Dual AAV vector approach for Duchenne muscular dystrophy
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September 11, 2023
Genethon’s Optidys project rewarded by BpiFrance as part of France 2030
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August 17, 2023
First results of Crigler-Najjar clinical trial published in New England Journal of Medicine
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July 12, 2023
Genethon and Thales collaborate on artificial intelligence to improve bioproduction efficiency
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May 30, 2023
Research work carried out at Genethon rewarded at the 26th edition of the ASGCT
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May 12, 2023
Genethon’s R&D to be Featured in Multiple Presentations at American Society of Gene & Cell Therapy Annual Meeting May 16-20, 2023, in Los Angeles, CA
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May 12, 2023
ILTOO Pharma and the MIROCALS Consortium announce the signing of Licence Agreement for the development of low dose interleukin-2 as a potential treatment for Amyotrophic Lateral Sclerosis (ALS)
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April 27, 2023
Crigler-Najjar syndrome: Hansa Biopharma and Genethon announce collaboration to develop imlifidase as pre-treatment to gene therapy for patients with anti-AAV antibodies
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March 6, 2023
Crigler-Najjar Syndrome: Genethon obtains PRIME priority drug status from the EMA for its gene therapy
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February 24, 2023
Chronic septic granulomatosis: biomarkers predict the efficacy of gene therapy
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February 7, 2023
"We made important achievements in 2022 but we still face key challenges in the year ahead"
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January 10, 2023
Genethon Launches Pivotal Clinical Trial of Gene Therapy for Crigler-Najjar Syndrome, a Rare Liver Disease
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December 14, 2022
Publication: Genethon helps clarify a molecular mechanism of mitochondrial malfunction in Duchenne muscular dystrophy
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November 21, 2022
Téléthon 2022: Benjamin, a hope for families thanks to clinical trials
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November 21, 2022
Téléthon 2022 : Benjamin, l’espoir des familles grâce aux essais cliniques
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November 21, 2022
Telethon 2022: for Lucie, "a real opportunity, thanks to advances in research"
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Serving the public interest
Our mission: Conception, clinic and preclinic development of drugs of genic therapy for rare diseases
Our goal: Providing these innovative treatments to the sick