RecruitingPhase 1NCT07037862
A Study in Participants With Duchenne Muscular Dystrophy Amenable to Exon 44 Skipping to Evaluate the Safety and Efficacy of ENTR-601-44
Studying Duchenne muscular dystrophy
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Entrada Therapeutics, Inc.
- Principal Investigator
- Entrada Therapeutics Clinical TrialsEntrada Therapeutics, Inc.
- Intervention
- ENTR-601-44(drug)
- Enrollment
- 24 enrolled
- Eligibility
- 4-20 years · MALE
- Timeline
- 2025 – 2029
Study locations (14)
- University Hospital Gent, Ghent, Belgium
- UZ Leuven, Leuven, Belgium
- Centre Hospitalier Régional de la Citadelle, Liège, Belgium
- IRCCS Ospedale San Raffaele, Milan, Italy
- Fondazione Serena Onlus - Centro Clinico NeMO Milano, Milan, Italy
- Ospedale Pediatrico Bambino Gesu, Rome, Italy
- Hospital Universitario Vall d'Hebron, Barcelona, Spain
- Hospital Sant Joan de Deu, Barcelona, Spain
- Leeds General Infirmary, Leeds, United Kingdom
- Alder Hey Children's NHS Foundation Trust, Liverpool, United Kingdom
- Great Ormond Street Hospital for Children, London, United Kingdom
- Royal Manchester Children's Hospital, Manchester, United Kingdom
- Freeman Hospital, Newcastle upon Tyne, United Kingdom
- Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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