Refractory Childhood Malignant Solid Neoplasm

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Review clinical trials related to Refractory Childhood Malignant Solid Neoplasm. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Testing the Addition of an Anti-cancer Drug, DT2216, to the Usual Chemotherapy Treatment for Relapsed or Refractory Solid Tumors and Fibrolamellar Carcinoma

This phase I/II trial tests the safety, side effects and best dose of DT2216 in combination with irinotecan and how well it works in treating children, adolescents and young adults with solid tumors and fibrolamellar cancer that has come back after a period of improvement (relapsed) or that has not responded to previous treatment (refractory). DT2216 is an anti-apoptotic protein B-cell lymphoma-extra large targeted protein degrader. It may stop the growth of tumor cells by blocking Bcl-xL, a protein needed for tumor cell survival. Irinotecan is in a class of antineoplastic medications called topoisomerase I inhibitors. It blocks a certain enzyme needed for cell division and deoxyribonucleic acid repair and may kill tumor cells. Giving DT2216 in combination with irinotecan may be safe, tolerable, and/or effective in treating children, adolescents and young adults with relapsed or refractory solid tumors or fibrolamellar cancer.

Participants needed: 81
Trial details
Phase: Phase 1, Phase 2Age: 1-39Biological sex: AllType: InterventionalSponsor: Children's Oncology GroupUpdated: May 5, 2026Locations: 21
Eligibility criteria

PHASE 1: Patients between ≥ 1 year and ≤ 21 years of age at the time of study en... [+43]

Pregnant or breast-feeding women will not be entered on this study due to risks... [+16]

Status: Recruiting

Ex Vivo Drug Sensitivity Testing and Multi-Omics Profiling

Functional precision medicine (FPM) is a relatively new approach to cancer therapy based on direct exposure of patient- isolated tumor cells to clinically approved drugs and integrates ex vivo drug sensitivity testing (DST) and genomic profiling to determine the optimal individualized therapy for cancer patients. In this study, we will enroll relapsed or refractory pediatric cancer patients with tissue available for DST and genomic profiling from the South Florida area, which is 69% Hispanic and 18% Black. Tumor cells collected from tissue taken during routine biopsy or surgery will be tested.

Participants needed: 65
Trial details
Phase: Phase 1Age: 1-21Biological sex: AllType: InterventionalSponsor: Florida International UniversityUpdated: Jul 11, 2025Locations: 1
Eligibility criteria

Patients aged 21 years or younger at the time of enrollment on this study of any...

Subjects who do not have malignant tissue available and accessible The amount of...