Enrolling by invitationPhase 2NCT06926621
A Study of Long-term Safety and Efficacy of VX-670 in Participants With Myotonic Dystrophy Type I
Studying Steinert myotonic 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
- Vertex Pharmaceuticals Incorporated
- Intervention
- VX-670(drug)
- Enrollment
- 44 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2025 – 2029
Study locations (11)
- Wesley Research Institute, Auchenflower, Australia
- Neuroscience Clinical Trials Unit, Alfred Brain, Melbourne, Australia
- Universitaire Ziekenhuizen Leuven - Campus Gasthuisberg - Pulmonology, Leuven, Belgium
- Altasciences Montreal, Montreal, Canada
- Montreal Neurological Institute-Hospital, Montreal, Canada
- University of Ottawa, Ottawa, Canada
- Universite Laval - Neurology, Québec, Canada
- Hospital Universitario y Politecnico La Fe - Neurology, Valencia, Spain
- Queen Elizabeth University Hospital - Neurology, Glasgow, United Kingdom
- Leonard Wolfson Experimental Neurology Centre CRF, London, United Kingdom
- Royal Hallamshire Hospital - Neurology, Sheffield, 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.
Open NCT06926621 on ClinicalTrials.govOther trials for Steinert myotonic dystrophy
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- RECRUITINGPHASE1, PHASE2NCT06185764A Phase 1/2 Study of VX-670 in Adult Participants With Myotonic Dystrophy 1 (DM1)Vertex Pharmaceuticals Incorporated
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- RECRUITINGNCT06075693Cerebrospinal Fluid Biomarkers of Myotonic DystrophyMassachusetts General Hospital
- ENROLLING BY INVITATIONNCT06979024A Registered Observational Cohort Study of Myotonic Dystrophy Type 1First Affiliated Hospital of Fujian Medical University