Enrolling by invitationPHASE2, PHASE3NCT06873035
An Interventional Study of Infigratinib in Children With Hypochondroplasia
Studying Hypochondroplasia
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
- QED Therapeutics, a BridgeBio company
- Intervention
- infigratinib 0.128 mg/kg/day(drug)
- Enrollment
- 24 enrolled
- Eligibility
- 3-18 years · All sexes
- Timeline
- 2025 – 2027
Study locations (22)
- UCSF Benioff Children's Hospital, Oakland, California, United States
- Childrens Hospital Colorado, Aurora, Colorado, United States
- Children's National Hospital, Washington D.C., District of Columbia, United States
- Johns Hopkins School of Medicine, Baltimore, Maryland, United States
- University of Missouri, Columbia, Missouri, United States
- Vanderbilt University Medical Center, Nashville, Tennessee, United States
- University of Wisconsin Madison - Waisman Center Bone Dysplasia Clinic, Madison, Wisconsin, United States
- Murdoch Children's Research Institute, Parkville, Victoria, Australia
- London Health Services Center - Children's Hospital of Western Ontario, London, Ontario, Canada
- Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada
- Université de Montréal - Centre Hospitalier Universitaire Sainte-Justine, Montreal, Quebec, Canada
- Hôpital Femme Mère Enfant, Bron, France, France
- Hôpital Universitaire Necker-Enfants Malades, Paris, France, France
- Centre Hospitalier Universitaire (CHU) de Toulouse - Hôpital des Enfants, Toulouse, France, France
- Haukeland University Hospital, Bergen, Norway, Norway
- +7 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.
Open NCT06873035 on ClinicalTrials.govOther trials for Hypochondroplasia
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