An Interventional Study of Infigratinib in Children With Hypochondroplasia
Part of paid clinical trials in Oakland, California.
- Sponsor
- QED Therapeutics, a BridgeBio company
- Study ID
- NCT06873035
- Phase
- PHASE2/PHASE3
- Status
- Enrolling By Invitation
Conditions
- Hypochondroplasia
Eligibility Criteria
- Sex
- ALL
- Age
- 3 Years - 18 Years
- Healthy Volunteers
- Not accepted
Interventions
- infigratinib 0.128 mg/kg/day — DRUGOral infigratinib 0.128 mg/kg/day
- infigratinib 0.25 mg/kg/day — DRUGOral infigratinib 0.25 mg/kg/day
Study Details
ACCEL2/3 is a Phase 2/3 study. The purpose of the Phase 2 portion of the study (ACCEL2/3) is to evaluate the efficacy and safety, of infigratinib in children with hypochondroplasia (HCH) receiving infigratinib, at one of two doses, of who have completed at least 26 weeks of participation in QED-sponsored ACCEL (QBGJ398-004).
Key Dates
- Start date
- Apr 22, 2025
- Status verified
- Mar 2025
- Primary completion
- Jan 31, 2027
- Completion
- Jan 31, 2027
Study Design
- Enrollment
- 24 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Phase 2 Cohort 1infigratinib (0.128 mg/kg/day)
- Experimental: Phase 2 Cohort 2infigratinib (0.25 mg/kg/day)
Primary Outcome Measure
Change from baseline (BL) in Annualized Height Velocity (AHV; cm/year) [ Time Frame: 26 weeks ]
Locations (7)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| UCSF Benioff Children's Hospital | Oakland | California | 94609 | - |
| Childrens Hospital Colorado | Aurora | Colorado | 80045 | - |
| Children's National Hospital | Washington D.C. | District of Columbia | 20010 | - |
| Johns Hopkins School of Medicine | Baltimore | Maryland | 21287 | - |
| University of Missouri | Columbia | Missouri | 65201 | - |
| Vanderbilt University Medical Center | Nashville | Tennessee | 37232 | - |
| University of Wisconsin Madison - Waisman Center Bone Dysplasia Clinic | Madison | Wisconsin | 53705 | - |
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