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OncoMatch/Clinical Trials/NCT05071937

ZEN003694 Combined With Talazoparib in Patients With Recurrent Ovarian Cancer

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

Phase 2RecruitingAlexander B Olawaiye, MDNCT05071937Data as of Jun 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

Treatments studied

Targeted therapy

Talazoparib

Other

ZEN003694

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)

Demographics

Female only

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 →

Frequently asked questions

Is NCT05071937 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior BET inhibitor disqualifies patients from enrollment.

Does this trial require BRCA1?

Yes, BRCA1 any tested is a required biomarker for enrollment.

Does this trial require BRCA2?

Yes, BRCA2 any tested is a required biomarker for enrollment.

Is this trial open to male patients?

No. This trial enrolls female patients only.

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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