OncoMatch/Clinical Trials/NCT06156410
Cabozantinib With Ifosfamide in Relapsed/Refractory Sarcomas
Is NCT06156410 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies Cabozantinib for ewing sarcoma.
Treatment: Cabozantinib — The purpose of this study is to better understand how safe and effective the drug cabozantinib in combination with high-dose ifosfamide is in the treatment of children and adults with relapsed/refractory sarcomas.
Check if I qualifyExtracted eligibility criteria
Cancer type
Sarcoma
Osteosarcoma
Prior therapy
Must have received: cytotoxic chemotherapy — upfront initial therapy
Disease that has progressed on or relapsed after upfront initial therapy, which must have included traditional chemotherapy
Cannot have received: cabozantinib (cabozantinib)
Exception: prior therapy with cabozantinib without progression/relapse and prior use of other multi-tyrosine kinase inhibitors is allowed
Prior progression/relapse with cabozantinib. Prior therapy with cabozantinib without progression/relapse and prior use of other multi-tyrosine kinase inhibitors is allowed.
Cannot have received: high-dose ifosfamide (ifosfamide)
Prior therapy with high-dose ifosfamide (> 10 g/m2/cycle) at any point.
Cannot have received: small molecule inhibitor
Any small molecule inhibitor therapy within 5 half-lives of the drug or 14 days, whichever is shorter, before enrollment.
Cannot have received: myelosuppressive chemotherapy
Myelosuppressive chemotherapy within 14 days before enrollment.
Cannot have received: autologous bone marrow transplant
Autologous bone marrow transplant (auto-BMT) within 42 days before enrollment.
Cannot have received: immunotherapy (CAR-T cell therapy)
Immunotherapy, including chimeric antigen receptor T-cells (CAR-T), within 21 days before enrollment.
Cannot have received: radiation therapy
Small port radiation therapy within 14 days before enrollment. Substantial bone marrow radiation (i.e. > 50% of the pelvis) or craniospinal radiation within 4 weeks before enrollment.
Cannot have received: major surgery
Major surgery (i.e. abdominal surgery; excluding intracranial surgery as noted above) within 14 days before enrollment. Minor surgeries (including mediport or tunneled catheter placement; excluding needle biopsy for tumor sampling or peripherally inserted central catheter placement) within 10 days before enrollment.
Cannot have received: hematopoietic growth factor
Hematopoietic growth factors within 7 days (for short-acting growth factor) or 14 days (for long-acting growth factor) before enrollment.
Lab requirements
Blood counts
ANC > 1,000/uL (without hematopoietic growth factor within the time frame noted below). Hemoglobin > 8 g/dL (without transfusion in the last 7 days). Platelets > 100,000/uL (without transfusion in the last 7 days).
Kidney function
Normal renal function by any of: serum creatinine < 1.5 x ULN for age; cystatin C within normal limits; nuclear medicine GFR within normal limits; or calculated creatinine clearance > 70 mL/min/1.73 m2. UPCR ≤ 1 mg/mg or 24-hour urine protein ≤ 1 g.
Liver function
Total bilirubin < 1.5 x ULN (for subjects with Gilbert's disease < 3.0 x ULN). ALT, AST, and ALP ≤ 3 x ULN (ALP ≤ 5 x ULN with documented bone metastases). Serum albumin > 2.8 g/dL. PT and PTT < 1.3 x ULN.
Hematopoietic function: ANC > 1,000/uL, Hemoglobin > 8 g/dL, Platelets > 100,000/uL. Renal function: see above. Hepatic function: see above.
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- University of California San Francisco · San Francisco, California
- Children's Hospital Colorado · Aurora, Colorado
- Children's Hospital of Philadelphia · Philadelphia, Pennsylvania
- University of Pennsylvania · Philadelphia, Pennsylvania
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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