drugset / Trial / NCT07441876

Study to Evaluate the Efficacy and Safety of BMN 333 Versus Vosoritide in Children With Achondroplasia

NCT07441876

Phase 2/3 Recruiting 160 enrolled BioMarin Pharmaceutical
RandomizedParallel-groupSingle-blindTreatment

Summary

This is a multicenter, multinational, randomized, active-controlled, operationally seamless Phase 2/3 study of BMN 333 in treatment-naïve pediatric participants with achondroplasia (ACH). The study consists of a Phase 2 part and a Phase 3 part.

Timeline

Start
2026-04-20
Primary completion
2029-06
Completion
2029-09

Drugs

EvaluationDrugModalityDoseRoute
Subject BMN 333 Unknown Subcutaneous
Comparator Vosoritide Peptide Subcutaneous

Indications