Active, not recruitingPhase 2NCT02724228
A Study to Evaluate Long-Term Safety, Tolerability, & Efficacy of BMN 111 in Children With Achondroplasia (ACH)
Studying Achondroplasia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- BioMarin Pharmaceutical
- Principal Investigator
- Medical Director, MDBioMarin Pharmaceutical
- Intervention
- BMN 111(drug)
- Enrollment
- 30 enrolled
- Eligibility
- 7 years · All sexes
- Timeline
- 2016 – 2028
Study locations (9)
- Children's Hospital & Research Center Oakland, Oakland, California, United States
- Harbor - UCLA Medical Center, Torrance, California, United States
- Ann and Robert H. Lurie Childrens Hospital of Chicago, Chicago, Illinois, United States
- Johns Hopkins McKusick - Institute of Genetic Medicine, Baltimore, Maryland, United States
- Vanderbilt University, Nashville, Tennessee, United States
- Baylor College of Medicine, Houston, Texas, United States
- Murdoch Children's Research Institute, Parkville, Victoria, Australia
- Institut Necker, Paris, France
- Guys & St. Thomas NHS Foundation Trust Evelina Hospital, London, United Kingdom
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.
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