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OncoMatch/Clinical Trials/NCT03900793

Losartan + Sunitinib in Treatment of Osteosarcoma

Is NCT03900793 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies multiple treatments including Losartan and Sunitinib for osteosarcoma.

Phase 1RecruitingUniversity of Colorado, DenverNCT03900793Data as of Jun 2026

Treatment: Losartan · SunitinibThis study is a Phase 1/1b clinical trial that aims to determine the Maximally Tolerated Dose of Losartan and Sunitinib Combination Therapy. Patients will first be accrued to the Dose Escalation phase of the study, using a 3+3 design. Medication dosages will increase until a maximally tolerated dose is found. Patients will then be accrued to the Dose Expansion phase of the trial, where efficacy of pre-determined dose will be preliminarily assessed.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Sunitinib

Other

Losartan

Cancer type

Osteosarcoma

Performance status

ECOG OR KARNOFSKY 0–2

ECOG performance status (≥18 years old) ≤ 2 or Karnofsky performance score (<18 years old) ≥ 50

Demographics

Ages ≥ 10

Prior therapy

Min 1 prior line

Lab requirements

Blood counts

Peripheral absolute neutrophil count (ANC) ≥ 750/mm3; Platelet count ≥ 75,000/mm3 (transfusion independent, defined as not receiving platelet transfusions for at least 7 days prior to enrollment); Hemoglobin ≥ 8 g/dL (with or without transfusion)

Kidney function

Creatinine clearance or radioisotope GFR > 70 mL/min/1.73 m2 OR a serum creatinine based on age/gender

Liver function

Total bilirubin ≤ 1.5 x ULN for age; SGPT (ALT) ≤ 135 U/L (ULN for SGPT is 45 U/L); Serum albumin ≥ 2.8 g/dL

Cardiac function

Current cardiac ejection fraction > 50% by biplane Simpson method on echocardiogram; QTc ≤ 480 ms

Adequate bone marrow function, defined as: Peripheral absolute neutrophil count (ANC) ≥ 750/mm3; Platelet count ≥ 75,000/mm3 (transfusion independent, defined as not receiving platelet transfusions for at least 7 days prior to enrollment); Hemoglobin ≥ 8 g/dL (with or without transfusion) Adequate renal function, defined as: Creatinine clearance or radioisotope GFR > 70 mL/min/1.73 m2 OR a serum creatinine based on age/gender. Adequate hepatic function, defined as: Total bilirubin ≤ 1.5 x upper limit of normal (ULN) for age; SGPT (ALT) ≤ 135 U/L. For the purpose of this study, the ULN for SGPT is 45 U/L; Serum albumin ≥ 2.8 g/dL Adequate cardiac function, defined as: Current cardiac ejection fraction > 50% by biplane Simpson method on echocardiogram; QTc ≤ 480 ms

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Children's Hospital Los Angeles · Los Angeles, California
  • Children's Hospital Colorado · Aurora, Colorado
  • University of Colorado Hospital · Aurora, Colorado
  • Children's Hospital of Atlanta · Atlanta, Georgia

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See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT03900793 currently recruiting?

Yes, this trial is currently recruiting patients.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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Related pages

Osteosarcoma trials