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By invitation only Phase 2 NCT06926621

A Study of Long-term Safety and Efficacy of VX-670 in Participants With Myotonic Dystrophy Type I

Phase 2 – studying effectiveness and dosage
Conditions: Myotonic Dystrophy Type 1 (DM1)

Sponsor: Vertex Pharmaceuticals Incorporated

trial.available_in: БГ
Overview
The purpose of the study is to evaluate the long-term safety and tolerability, efficacy and pharmacokinetics of VX-670 in participants with Myotonic Dystrophy Type I (DM1).
Who can participate
Key Inclusion Criteria: • Completed study drug treatment in parent study VX23-670-001 (NCT06185764) Key Exclusion Criteria: • History of any illness or any clinical condition as pre-specified in the protocol Other protocol defined Inclusion/Exclusion criteria may apply.
Locations 5
Australia (1)
Wesley Research Institute
Auchenflower
Belgium (1)
Universitaire Ziekenhuizen Leuven - Campus Gasthuisberg - Pulmonology
Leuven
Canada (1)
Altasciences Montreal
Montreal
Spain (1)
Hospital Universitario y Politecnico La Fe - Neurology
Valencia
United Kingdom (1)
Queen Elizabeth University Hospital - Neurology
Glasgow
Technical details
Status
By invitation only
Phase
Phase 2
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
28.04.2025
Completion date
30.01.2029
Registry ID
NCT06926621
Source
anzctr
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Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.