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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.

Phase 1RecruitingChildren's Hospital of PhiladelphiaNCT06156410Data as of May 2026

Treatment: CabozantinibThe 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.

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Extracted eligibility criteria

Cancer type

Sarcoma

Osteosarcoma

Prior therapy

Min 1 prior line

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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