OncoMatch

OncoMatch/Clinical Trials/NCT05071937

ZEN003694 Combined With Talazoparib in Patients With Recurrent Ovarian Cancer

Is NCT05071937 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including ZEN003694 and Talazoparib for ovarian cancer.

Phase 2RecruitingAlexander B Olawaiye, MDNCT05071937Data as of May 2026

Treatment: ZEN003694 · TalazoparibThis Phase 2, open label, study with safety lead in of oral talazoparib in combination with ZEN003694 given daily in 28-day cycles will enroll patients with recurrent ovarian, fallopian tube or primary peritoneal carcinoma.

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Extracted eligibility criteria

Cancer type

Ovarian Cancer

Biomarker criteria

Required: BRCA1 any tested

Known BRCA1/2 status

Required: BRCA2 any tested

Known BRCA1/2 status

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 1 prior line

Must have received: PARP inhibitor — maintenance or therapeutic

Prior therapy with PARPi either as maintenance or therapeutic settings.

Cannot have received: BET inhibitor (ZEN003694)

Have previously received an investigational BET inhibitor (including previous participation in studies with Zenith drug, ZEN003694)

Lab requirements

Blood counts

Hemoglobin  9.0 gm/dL without transfusions during the 4 weeks prior to Screening; ANC  1.5 d7 10^9/L; Platelet count  150,000/mm3

Kidney function

Serum Creatinine  1.5 X ULN

Liver function

AST or ALT  2.0 x ULN or if liver function abnormalities due to liver metastases AST and ALT  5.0 x ULN; Total bilirubin  1.5 x ULN ( 3.0 x ULN for subjects with known Gilbert's syndrome)

Cardiac function

QTcF interval  470 msec

Adequate laboratory parameters at Screening including: Hemoglobin  9.0 gm/dL without transfusions during the 4 weeks prior to Screening; ANC  1.5 d7 10^9/L; Platelet count  150,000/mm3; AST or ALT  2.0 x ULN or if liver function abnormalities due to liver metastases AST and ALT  5.0 x ULN; Total bilirubin  1.5 x ULN ( 3.0 x ULN for subjects with known Gilbert's syndrome); Serum Creatinine  1.5 X ULN; Prothrombin time (PT), INR and PTT < 1.5 x ULN; QTcF interval  470 msec

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

US trial sites

  • University of Pittsburgh Medical Center · Pittsburgh, Pennsylvania

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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