drugset / Trial / NCT07573631

An Open-Label Extension Study to Evaluate the Long-term Safety and Efficacy of BMN 351 in Participants With Duchenne Muscular Dystrophy

NCT07573631 ↗

Phase 2 Enrolling by invitation 18 enrolled BioMarin Pharmaceutical
NaSingle-groupOpen-labelTreatment

Summary

This open-label extension study aims to evaluate the long-term safety and tolerability of weekly BMN 351 infusions, as well as to assess the effect of BMN 351 on physical function, in participants with DMD who participated in the 351-201 study.

Timeline

Start
2026-04
Primary completion
2031-12
Completion
2031-12

Drugs

EvaluationDrugModalityDoseRoute
Subject BMN 351 Antisense oligonucleotide — Intravenous