drugset / Trial / NCT06926621

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

NCT06926621 ↗

Phase 2 Enrolling by invitation 44 enrolled Vertex Pharmaceuticals Incorporated
NaSingle-groupOpen-labelTreatment

Summary

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).

Timeline

Start
2025-04-28
Primary completion
2029-01-30
Completion
2029-01-30

Drugs

EvaluationDrugModalityDoseRoute
Subject VX-670 Unknown — Intravenous