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OncoMatch/Clinical Trials/NCT05128825

A Study of Azenosertib (ZN-c3) in Subjects With Platinum-Resistant High-Grade Serous Ovarian, Fallopian Tube or Primary Peritoneal Cancer

Is NCT05128825 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies azenosertib for high-grade serous ovarian, fallopian tube or primary peritoneal cancer.

Phase 2RecruitingK-Group, Beta, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals, IncNCT05128825Data as of May 2026

Treatment: azenosertibThis is a multi-part Phase 2 study to evaluate the efficacy and safety of azenosertib (ZN-c3) in subjects with Platinum-Resistant, High-Grade Serous Ovarian, Fallopian Tube, or Primary Peritoneal Cancer. Part 2 of the study will be conducted in subjects whose tumors are Cyclin E1 positive as determined by central review using the Sponsor's investigational clinical trial assay.

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Extracted eligibility criteria

Cancer type

Ovarian Cancer

Biomarker criteria

Required: CCNE1 protein overexpression (positive Cyclin E1 protein status by IHC using Sponsor's assay)

Tumor testing (archival acceptable) confirms a positive Cyclin E1 protein status result determined by IHC using the Sponsor's investigational clinical trial assay

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Max 3 prior lines
Min 1 prior line

Must have received: bevacizumab (bevacizumab) — if eligible per standard of care

Prior bevacizumab treatment is required, if eligible per standard of care

Must have received: PARP inhibitor — if BRCA 1/2 mutation or HRD, if eligible per standard of care

Prior PARP inhibitor treatment is required if BRCA 1/2 mutation or HRD, if eligible per standard of care

Must have received: mirvetuximab (mirvetuximab) — if eligible per standard of care

Prior mirvetuximab treatment is required, if eligible per standard of care

Cannot have received: WEE1 inhibitor (ZN-c3)

Prior therapy with ZN-c3 or any other WEE1 inhibitor, ATR inhibitor, PKMYT1 inhibitor, or CHK1/2 inhibitor.

Cannot have received: ATR inhibitor

Prior therapy with ZN-c3 or any other WEE1 inhibitor, ATR inhibitor, PKMYT1 inhibitor, or CHK1/2 inhibitor.

Cannot have received: PKMYT1 inhibitor

Prior therapy with ZN-c3 or any other WEE1 inhibitor, ATR inhibitor, PKMYT1 inhibitor, or CHK1/2 inhibitor.

Cannot have received: CHK1/2 inhibitor

Prior therapy with ZN-c3 or any other WEE1 inhibitor, ATR inhibitor, PKMYT1 inhibitor, or CHK1/2 inhibitor.

Lab requirements

Blood counts

Adequate hematologic function, as defined in protocol

Kidney function

Adequate organ function, as defined in protocol

Liver function

Adequate organ function, as defined in protocol

Adequate hematologic and organ function, as defined in protocol

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

US trial sites

  • Site 0170-USA Mitchell Cancer Institute · Mobile, Alabama
  • Site 0143 - HonorHealth · Phoenix, Arizona
  • Site 0102 - University of Arizona Cancer Center · Tucson, Arizona
  • Site 0258 - UC San Diego Moores Cancer Center · La Jolla, California
  • Site 0287 - Ridley Tree Cancer Center · Santa Barbara, California

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

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