Active, not recruitingPhase 2NCT03989947
An Extension Study to Evaluate Safety and Efficacy of BMN 111 in Children With Achondroplasia
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
- Active BMN 111: Subcutaneous injection of recommended dose of BMN 111 based on weight-band dosing once daily.(drug)
- Enrollment
- 73 enrolled
- Eligibility
- All sexes
- Timeline
- 2019 – 2038
Study locations (16)
- Children's Hospital & Research Center Oakland, Oakland, California, United States
- Harbor - UCLA Medical Center, Torrance, California, United States
- Alfred I. duPont Hospital for Children, Wilmington, Delaware, United States
- Emory University, Decatur, Georgia, United States
- Ann Robert and H. Lurie Children's Hospital of Chicago, Chicago, Illinois, United States
- Cincinnati Childrens Hospital, Cincinnati, Ohio, United States
- Vanderbilt University Medical Center, Nashville, Tennessee, United States
- Baylor College of Medicine, Houston, Texas, United States
- Medical College of Wisconsin, Children's Hospital, Milwaukee, Wisconsin, United States
- The Children's Hospital at Westmead, Westmead, New South Wales, Australia
- Murdoch Children's Research Institute, Parkville, Victoria, Australia
- Osaka University, Osaka, Japan
- Saitama Children's Medical Center, Saitama, Japan
- Tokushima University Hospital, Tokushima, Japan
- Guy's and St. Thomas NHS Foundation Trust Evelina Children's Hospital, London, United Kingdom
- +1 more locations on ClinicalTrials.gov
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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