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OncoMatch/Clinical Trials/NCT06942442

A Phase II Trial of Tebentafusp in HLA-A*02:01 Positive Patients With Advanced Clear Cell Sarcoma

Is NCT06942442 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Physician's Choice and Tebentafusp for hla-a*0201 positive cells present.

Phase 2RecruitingSarcoma Alliance for Research through CollaborationNCT06942442Data as of May 2026

Treatment: Physician's Choice · TebentafuspThis is a multi-center, open label, phase II study of tebentafusp in patients with unresectable or metastatic clear cell sarcoma (CCS).

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Extracted eligibility criteria

Cancer type

Sarcoma

Biomarker criteria

Required: HLA-A A*02:01 positive

HLA-A*02:01 positive

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Lab requirements

Blood counts

Absolute Neutrophil Count (ANC) ≥ 1.5; Platelets ≥ 75

Kidney function

Serum creatinine ≤ 1.5 x institutional ULN or 24-hour creatinine clearance ≥ 50 ml/min (Cockroft formula acceptable)

Liver function

ALT and AST ≤ 2.5 x institutional ULN or ≤ 5.0 x institutional ULN if considered due to tumor; Alkaline phosphatase ≤ 2.5 x institutional ULN unless considered due to tumor; Serum bilirubin ≤ 1.5 x institutional ULN (patients with elevated bilirubin secondary to Gilbert's disease are eligible)

Adequate organ function within 28 days of Day 1 of study defined as: Absolute Neutrophil Count (ANC) ≥ 1.5; Platelets ≥ 75; ALT and AST ≤ 2.5 x institutional ULN or ≤ 5.0 x institutional ULN if considered due to tumor; Alkaline phosphatase ≤ 2.5 x institutional ULN unless considered due to tumor; Serum bilirubin ≤ 1.5 x institutional ULN. NOTE: Patients with elevated bilirubin secondary to Gilbert's disease are eligible to participate in the study; Serum creatinine ≤ 1.5 x institutional ULN or 24-hour creatinine clearance ≥ 50 ml/min (calculated creatinine clearance using Cockroft formula is acceptable)

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

US trial sites

  • University of Southern California - Norris Cancer Center · Los Angeles, California
  • Memorial Sloan Kettering Cancer Center · New York, New York

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