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OncoMatch/Clinical Trials/NCT07032285

Cirtuvivint in Selected Advanced Soft-Tissue Sarcomas

Is NCT07032285 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Cirtuvivint for soft tissue sarcoma (sts).

Phase 2RecruitingAsociación Europea y Latinoamericana SELNET para la Investigación en SarcomasNCT07032285Data as of May 2026

Treatment: CirtuvivintThe study is a Phase 2 clinical trial of the drug cirtuvivint as a second-line treatment for advanced soft tissue sarcomas. The study is being conducted in Spain and is expected to enroll approximately 25 patients in total. The primary objective of this Phase 2 study is to evaluate the efficacy of treatment with cirtuvivint. Cirtuvivint is an anti-cancer medication developed by the U.S. company Biosplice Therapeutics, Inc. This drug is an inhibitor of the enzymes CLK1-4 and DYRK1-4 (molecules involved in the cell cycle) and is administered as oral tablets. This product is still under investigation and has not yet been approved in Europe.

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Extracted eligibility criteria

Cancer type

Sarcoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Max 3 prior lines
Min 1 prior line

Must have received: anthracycline

Patients should have received at least anthracyclines previously unless not indicated (SFT)

Cannot have received: CLK inhibitor

Previous treatment with CLK inhibitors

Cannot have received: other anti-cancer therapy or investigational product

Patients who have received any other anti-cancer therapy or investigational product in the last 28 days prior to enrollment

Lab requirements

Blood counts

Absolute neutrophil count ≥1,500/mm³; Platelet count ≥100,000/mm³

Kidney function

Creatinine ≤1.5 mg/dL

Liver function

AST and ALT ≤2.5 times upper limit of normal; Bilirubin ≤1.5 mg/dL

Cardiac function

Left ventricular ejection fraction ≥50% by echocardiogram or MUGA scan

Adequate hepatic, renal, cardiac, and hematologic function. Laboratory tests as follows: Absolute neutrophil count ≥1,500/mm³; Platelet count ≥100,000/mm³; Bilirubin ≤1.5 mg/dL; AST and ALT ≤2.5 times upper limit of normal; Creatinine ≤1.5 mg/dL. Left ventricular ejection fraction ≥50% by echocardiogram or MUGA scan.

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

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