Enrolling by invitationPhase 3NCT06549400
An Open-Label Extension Study to Evaluate the Long-Term Safety and Efficacy of Once Daily Mexiletine PR in Patients With Myotonic Dystrophy Type 1 and Type 2 Who Have Completed MEX-DM-302 Study.
Studying Proximal myotonic myopathy
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
- Lupin Ltd.
- Intervention
- Mexiletine granules for prolonged-release oral suspension(drug)
- Enrollment
- 176 enrolled
- Eligibility
- 16 years · All sexes
- Timeline
- 2025 – 2028
Study locations (6)
- Laboratory for Muscle Diseases and Neuropathies, Leuven, Belgium
- Aarhus University Hospital, Aarhus, Denmark
- Ludug-Maximilians University, München, Germany
- Azienda Ospedaliera Universitaria Policlinico Tor Vergata, Rome, Italy
- University Hospital of Madrid, Madrid, Spain
- University College Hospital, London, United Kingdom
Collaborators
Lupin Atlantis Holdings S.A.
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 NCT06549400 on ClinicalTrials.govOther trials for Proximal myotonic myopathy
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