Active, not recruitingPhase 3NCT05394116

A Study to Assess Safety, Tolerability and Efficacy of Garetosmab Versus Placebo Administered Intravenously (IV) in Adult Participants With Fibrodysplasia Ossificans Progressiva (FOP)

Studying Fibrodysplasia ossificans progressiva

Last synced from ClinicalTrials.gov

Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing data

Key facts

Sponsor
Regeneron Pharmaceuticals
Principal Investigator
Clinical Trial Management
Regeneron Pharmaceuticals
Intervention
Garetosmab(drug)
Enrollment
63 enrolled
Eligibility
18 years · All sexes
Timeline
20222029

Study locations (22)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT05394116 on ClinicalTrials.gov

Other trials for Fibrodysplasia ossificans progressiva

Additional recruiting or active studies for the same condition.

See all trials for Fibrodysplasia ossificans progressiva

← Back to all trials