NCT03189706Active, not recruitingEarly phase 1
Study of Chemoimmunotherapy for High-Risk Neuroblastoma
Phase II Study of Hu3F8, Irinotecan/Temozolomide and Sargramostim (HITS) Chemoimmunotherapy for High-Risk Neuroblastoma
Source: ClinicalTrials.gov · Last updated 6 Jul 2026
Brief summary (registry, in English)
The purpose of this study is to find out whether an experimental drug called Hu3F8 can be given with the chemotherapy drugs irinotecan and temozolomide and another drug called GM-CSF. The investigators want to find out if this combination is safe and what effect it has on the participant and the disease.
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Early phase 1
- Study type
- Interventional
- Enrollment
- 48 (actual)
- First submitted
- 13 Jun 2017
- Start date
- 12 Jun 2017
- Primary completion date
- 30 Jun 2027
- Lead sponsor
- Memorial Sloan Kettering Cancer Center
- Diseases
- Neuroblastoma, Childhood cancers
- NCT number
- NCT03189706
What you commit to
- Study type: Interventional · Early phase 1
- Participants enrolled: 48
- From 12 Jun 2017 to the primary completion date, 30 Jun 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Patients with CR/VGPR disease
- Existing severe major organ dysfunction, i.e., renal, cardiac, hepatic, neurologic, pulmonary, or gastrointestinal toxicity ≥ grade 3 except for hearing loss, alopecia, anorexia, nausea, and hypomagnesemia from TPN, which may be grade 3
- History of allergy to mouse proteins
- Active life-threatening infection
Lab values
- ANC \< 500/uL
- Platelet count \<30K/uL
Other
- Inability to comply with protocol requirements
- Women who are pregnant or breast-feeding
Who the study is looking for
- Diagnosis of NB as defined by international criteria,.e., histopathology (confirmed by the MSK Department of Pathology) or bone marrow metastases plus high urine catecholamine levels
- High-risk NB as defined as any of the following:
- Stage 4 with MYCN amplification (any age)
- Stage 4 without MYCN amplification (\>1.5 years of age)
- Stage 3 with MYCN amplification (unresectable; any age)
- Stage 4S with MYCN amplification (any age)
- Patients fulfill one of the following criteria:
- Have evidence of soft tissue disease OR
- If they only have osteomedullary disease at protocol enrollment, they should have:
- Had previously received Hu3F8+GMCSF therapy AND have had less than a complete response to it OR
- Had progressed progressive disease after their most recent anti-neuroblastoma therapeutic regimen
- Patients must have evaluable (microscopic marrow metastasis, elevated tumor markers, positive MIBG or PET scans) or measurable (CT, MRI) disease documented after completion of prior systemic therapy.
- Prior treatment with murine and hu3F8 is allowed.
- Prior treatment with irinotecan or temozolomide is permitted.
- Patients with prior m3F8, hu3F8, ch14.18 or hu14.18 treatment must have a negative HAHA antibody titer. Human anti-mouse antibody positivity is allowed.
- Signed informed consent indicating awareness of the investigational nature of this program.
Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Memorial Sloan-Kettering Cancer Center Coordinator of this site? Confirm its status | New York | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.