← Back to all trials
Recruiting
NCT07767630
Safety, Tolerability, and Preliminary Efficacy of [211At]MABG in Patients With Relapsed or Refractory Neuroblastoma
Conditions: Neuroblastoma (NB)
Sex: All
Ages: 1 Year – 100 Years
Healthy volunteers: No
Phase: EARLY_PHASE1
Enrollment: 10
Sponsor: Sichuan University
Location: West China Hospital Chengdu Sichuan
Summary
Fractionated dosing of \[211At\]MABG Radiotherapy in Relapsed/Refractory Neuroblastoma
Eligibility Criteria
Inclusion Criteria:
1. Patients diagnosed with MIBG avid lesions, high-risk neuroblastoma per the Revised International Neuroblastoma Response Criteria (Revised INRC), with refractory, relapsed, or progressive disease.
2. All measurable soft tissue lesions must be MIBG-avid.
3. Age ≥ 1 year at enrollment.
4. Lansky performance status ≥ 50%.
5. Adequate organ function and hematologic parameters.
Exclusion Criteria:
1. Antibody-based immunotherapy within fewer than 5 half-lives or 30 days (whichever is shorter), or who have not yet recovered from adverse effects of any biologic therapy.
2. Treatment with \[¹³¹I\]MIBG or Lu177 targeted radionuclide therapy less than 3 months of last administration.
3. Autologous stem cell transplant \50% of bone marrow area) within 12 weeks prior to the first study dose.
5. Renal Insufficiency.
6. Active Infections.
Source: ClinicalTrials.gov (NCT07767630). StuddyBuddy aggregates publicly available trial information.