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Clinical Trial ● Currently Recruiting Phase II / Phase III NCT07441876

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

Study to Evaluate the Efficacy and Safety of BMN 333 Versus Vosoritide in Children With Achondroplasia — Recruiting • Phase II / Phase III • NCT07441876.

📅 24 Sep 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase II / Phase III
NCT ID
NCT07441876
Start
2026-04-20
Completion
2029-06
ClinicaliQ Trial Snapshot
  • Study to Evaluate the Efficacy and Safety of BMN 333 Versus Vosoritide in Children With Achondroplasia — Recruiting • Phase II / Phase III • NCT07441876.
  • Comparing two growth-boosting drugs (BMN 333 and vosoritide) in children with achondroplasia to see which works better and is safer.

Verify eligibility, endpoints and current status on the original ClinicalTrials.gov registry before acting on this summary.

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  • Quick orientation before opening the registry record.
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What This Trial Is Studying

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. Conditions: Achondroplasia Interventions: BMN 333, Vosoritide Injection [Voxzogo] Lead Sponsor: BioMarin Pharmaceutical Planned Enrollment: 160 participants

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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