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

PHASE2Not yet recruitingINTERVENTIONAL
Enrollment

47

Participants

Timeline

Start Date

August 25, 2025

Primary Completion Date

August 1, 2030

Study Completion Date

August 1, 2030

Conditions
HLA-A*0201 Positive Cells PresentClear Cell Sarcoma (CCS)
Interventions
DRUG

Physician's Choice

Patients who are HLA-A\*02:01-negative and ineligible to receive tebentafusp will be prospectively enrolled onto a separate study arm and treated with physicians' choice of treatment. They will also be radiographically assessed at the same schedule as patients treated with tebentafusp, if feasible, and kept on this treatment arm until progression of disease or unacceptable toxicity on the physicians' choice regimen.

DRUG

Tebentafusp

Patients who screen positive for HLA-A\*02:01 and meet the eligibility requirements will be treated with weekly tebentafusp

All Listed Sponsors
collaborator

Royal Marsden NHS Foundation Trust

OTHER

collaborator

Memorial Sloan Kettering Cancer Center

OTHER

lead

Sarcoma Alliance for Research through Collaboration

OTHER