Clin2
NCT03126916Possibly a fitRecruiting

Testing added therapy for high-risk neuroblastoma in children

GanglioneuroblastomaGanglioneuroblastoma, NodularNeuroblastoma

Treatments studied

Part of Cancer clinical trials.

This Phase 3 study tests whether adding either a targeted drug (lorlatinib) or a radioactive treatment (131I-MIBG) to intensive chemotherapy improves outcomes for children with high-risk neuroblastoma. It may help by aiming at tumor cells more directly alongside standard treatment.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
750 people
Ages
12 months to 30 years
Study type
Interventional

Who can take part

  • Your child must have a confirmed diagnosis of neuroblastoma or ganglioneuroblastoma (verified by tumor testing or a bone marrow finding plus urine tumor markers).
  • Your child must be between about 1 year old and 30 years old at diagnosis (and meet specific high-risk risk-group details for eligibility).
  • Your child should be considered “high-risk” and usually should not have had prior whole-body (systemic) treatment for high-risk disease, except very limited, allowed situations.
  • Your child must have adequate organ function, including blood-filtering kidney function and liver enzyme levels within the study limits.
  • Your child must have a strong-enough heart pumping function on echocardiogram (ultrasound of the heart).
  • If joining the lorlatinib (ALK) portion (Arm E), your child’s tumor must have an ALK alteration, and they must not have previously taken lorlatinib or another ALK inhibitor.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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