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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.

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07767630). StuddyBuddy aggregates publicly available trial information.