A Safety and Efficacy Study of hu14 in High-Risk Neuroblastoma Patients
Part of paid clinical trials in Aurora, Colorado.
- Sponsor
- Renaissance Pharma Ltd.
- Study ID
- NCT07549321
- Phase
- PHASE2/PHASE3
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Months - 18 Years
- Healthy Volunteers
- Not accepted
Interventions
- hu1418K322A + Temozolomide + Irinotecan — DRUG21-day cycle for a maximum of 12 cycles
Study Details
Neuroblastoma is the most common type of solid cancer found outside the brain in young children. Generally, it affects children younger than 5 years old, with the average age when it is found being just 2 years. Most patients have 'high-risk' disease, with spread of the disease to different sites (metastases). This multinational study aims to find out how effective and safe the treatment of a monoclonal anti-GD2 antibody hu14.18K322A (daretabart) is when used together with chemotherapy to treat children and young people who have high-risk neuroblastoma.
Key Dates
- Start date
- Apr 30, 2026
- Status verified
- Apr 2026
- Primary completion
- Mar 31, 2031
- Completion
- Mar 31, 2031
Study Design
- Enrollment
- 144 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Other: Higher dose
- Other: Lower dose
Primary Outcome Measure
Overall response rate (ORR) [ Time Frame: Assessed at end of treatment (up to 12 months) ]
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Children's Hospital Colorado Anschutz Medical | Aurora | Colorado | 80045 | |
| Children's Hospital of Philadelphia | Philadelphia | Pennsylvania | 19104 |
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