GENETHON
- Country
- 🇫🇷France
- Ownership
- Private
- Established
- 1990-01-01
- Employees
- 501
- Market Cap
- -
- Website
- http://www.genethon.fr
Clinical Trials
26
Trial Phases
3 Phases
Drug Approvals
0
Drug Approvals
No drug approvals found
This company may not have drug approvals in our database
Clinical Trials
Distribution across different clinical trial phases (21 trials with phase data)• Click on a phase to view related trials
Efficacy and Safety of GNT0003 Following Imlifidase Pre-treatment in Severe Crigler-Najjar Syndrome
- First Posted Date
- 2024-07-24
- Last Posted Date
- 2024-12-03
- Lead Sponsor
- Genethon
- Target Recruit Count
- 3
- Registration Number
- NCT06518005
- Locations
- 🇫🇷
Hopital Antoine BECLERE, Clamart, France
Natural History of Duchenne Muscular Dystrophy
- Conditions
- Duchenne Muscular Dystrophy
- First Posted Date
- 2019-03-20
- Last Posted Date
- 2022-09-07
- Lead Sponsor
- Genethon
- Target Recruit Count
- 100
- Registration Number
- NCT03882827
- Locations
- 🇫🇷
University Hospital of Bordeaux, Bordeaux, France
🇫🇷Brest University Hospital Centre, Brest, France
🇫🇷Hopital Femme Mere Enfant, Bron, France
Natural History Study of Patients With Limb-Girdle Muscular Dystrophy 2I
- Conditions
- LGMD2I
- First Posted Date
- 2019-02-15
- Last Posted Date
- 2023-04-06
- Lead Sponsor
- Genethon
- Target Recruit Count
- 52
- Registration Number
- NCT03842878
- Locations
- 🇩🇰
Pr John Vissing, Copenhagen, Denmark
🇫🇷Dr Tanya Stojkovic, Paris, France
🇬🇧Pr Volker Straub, Newcastle, United Kingdom
Gene Therapy for Severe Crigler Najjar Syndrome
- Conditions
- Crigler-Najjar Syndrome
- First Posted Date
- 2018-03-15
- Last Posted Date
- 2023-03-28
- Lead Sponsor
- Genethon
- Target Recruit Count
- 17
- Registration Number
- NCT03466463
- Locations
- 🇫🇷
Hopital Antoine BECLERE, Clamart, France
🇮🇹ASST Papa Giovanni XXIII, Bergame, Italy
🇮🇹Azienda Ospedaliera Universitaria Federico II, Napoli, Italy
Gene Therapy for X-linked Chronic Granulomatous Disease
- Conditions
- X-Linked Chronic Granulomatous Disease
- First Posted Date
- 2016-05-02
- Last Posted Date
- 2023-04-06
- Lead Sponsor
- Genethon
- Target Recruit Count
- 3
- Registration Number
- NCT02757911
- Locations
- 🇫🇷
Hôpital Necker Enfants Malades, Paris, France
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- 1
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News
Hansa Biopharma's Imlifidase Shows Promise in Guillain-Barré Syndrome and Anti-GBM Disease
• Hansa Biopharma announced positive Phase 2 results for imlifidase in Guillain-Barré Syndrome (GBS), showing rapid functional improvement in patients. • The company completed enrollment in the pivotal Phase 3 GOOD-IDES-02 trial of imlifidase for anti-glomerular basement membrane (anti-GBM) disease. • A Phase 2 trial of imlifidase as a pre-treatment to GNT-0003 in severe Crigler-Najjar syndrome has been initiated in collaboration with Genethon. • Hansa Biopharma anticipates submitting a Biologics License Application (BLA) to the FDA for imlifidase in kidney transplantation in late 2025.
Imlifidase Shows Promise in Guillain-Barré Syndrome and Expands Gene Therapy Access
• Phase 2 data indicates imlifidase, combined with IVIg, significantly improves motor function and accelerates recovery in Guillain-Barré Syndrome (GBS) patients. • An indirect comparison showed GBS patients treated with imlifidase and IVIg returned to independent walking six weeks sooner than those treated with IVIg alone. • Hansa Biopharma and Genethon initiated a Phase 2 trial using imlifidase as a pretreatment to broaden access to gene therapy for Crigler-Najjar syndrome. • Hansa Biopharma completed enrollment in a Phase 3 trial of imlifidase for anti-GBM disease, with data expected in 2025.
Genethon's GNT0004 Gene Therapy Shows Promise in Duchenne Muscular Dystrophy Trial
Genethon's GNT0004, a gene therapy for Duchenne muscular dystrophy (DMD), demonstrates positive initial results in a Phase 1/2/3 clinical trial, showing stable or improved motor function in treated patients.
Genethon's AAV Gene Therapy GNT0004 Shows Promise in Duchenne Muscular Dystrophy Trial
Genethon's GNT0004 gene therapy demonstrated good tolerability in boys with Duchenne muscular dystrophy when combined with transient immunological prophylactic treatment.