Study title:
A phase 3 multinational, open-label, systemic gene delivery study to evaluate the safety and efficacy of SRP-9003 in subjects with limb girdle muscular dystrophy 2E/R4
Long title:
A phase 3 multinational, open-label, systemic gene delivery study to evaluate the safety and efficacy of SRP-9003 in subjects with limb girdle muscular dystrophy 2E/R4
Date receipt dossier:
9 Feb 2024
EU record number:
B/BE/24/BVW4
EudraCT number:
2022-503112-17-00
Company / Sponsor:
Sarepta Therapeutics
Phase:
III
Treated organism:
Humans
Indication category:
Neuromuscular disorders
Disease:
Treatment of Limb Girdle Muscular Dystrophy
Therapeutic approach:
Gene therapy
Genetic modification:
Non-replicating recombinant vector derived from adeno-associated virus AAV, serotype rh74, lacking all AAV viral genes and carrying the full-length sarcoglycan-beta (SGCB) gene
Method of transfer of nucleic acid of interest:
Non-replicating recombinant vector derived from adeno-associated virus serotype rh74
Administered biological material:
Genetically modified virus
Route of administration:
Intravenous
Locations in Belgium:
UZ Leuven, UZ Gent
Nr of subjects:
Up to 15 patients overall and 4 patients in Belgium
Foreseen duration:
from May 2024 till End January 2031
Type of procedure:
Contained use and Deliberate release
Current status:
Under evaluation
Information for the public
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Public information according to the provisions of Directive 2001/18/EC
Information related to the decision procedure
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27 May 2024 - The Biosafety Advisory Council issues a positive advice (with conditions) for this deliberate release
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21 June 2024 - The Federal Ministers give a final decision (positive with conditions) for this trial