Clinical Analysis of Naxitamab (hu3F8) in the Treatment of Pediatric High Risk or Refractory/ Relapsed Neuroblastoma
Condition(s) studied
Investigational drug(s) / intervention(s)
Naxitamab monotherapy: Naxitamab is administered on days 1, 3, and 5
GM-CSF: Each treatment cycle is 28 days and is started with five days (days -4 to 0) of GM-CSF administered at 250 mcg/m2/day in advance of the start of naxitamab infusion. GM-CSF is thereafter administered at 500 mcg/m2/day on days 1 to 5.
Irinotecan: Each HITS treatment cycle is 21 days. Irinotecan intravenously (IV) at 50 mg/m2/day will be administered from Day 1-5 concurrently with temozolomide orally at 150 mg/m2/day or 100 mg/m2/day.
Temozolomide: Each HITS treatment cycle is 21 days. Irinotecan intravenously (IV) at 50 mg/m2/day will be administered from Day 1-5 concurrently with temozolomide orally at 150 mg/m2/day or 100 mg/m2/day.
Naxitamab in combination therapy: Naxitamab 2.25mg/kg IV will be administered on Days 2, 4, 8 and 10.
GM-CSF with combination regimen: GM-CSF 250 mcg/m2/day will be administered subcutaneously on Days 6-10.
Sintilimab: Sintilimab was administerd with 3mg/kg (max 200mg) on day 11 every 3 weeks.
Study summary
This is an prospective study to evaluate the safety and efficacy of naxitamab monotherapy or combined with chemotherapy or combined with chemotherapy and checkpoint inhibitor in the treatment of pediatric high-risk and refractory/relapsed neuroblastoma in Sun Yat-sen University Cancer Center.
Eligibility
Primary outcome measure(s)
- ORR — from start of naxitamab treatment to 1.5 years after EOT
The proportion of patients who achieved CR or PR
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Sun Yat-sen University Cancer Center | Guangzhou | Guangdong | Recruiting |
More Sun Yat-Sen University Cancer Center trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06013618 on ClinicalTrials.gov ↗ ← All trials in China