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NCT05065021

Using Genetic Profile to Determine the Treatment for Patients With Ovarian Cancer Who Previously Received a PARP-inhibitor

Status unknown Phase 2 Last updated 17 January 2024
What this trial tests

Phase 2 trial testing Niraparib in Ovarian Cancer in 40 participants. Status unknown.

Timeline
23 February 2023
Primary endpoint
6 June 2025
6 June 2025

Quick facts

Lead sponsorUniversity Health Network, Toronto
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment40
Start date23 February 2023
Primary completion6 June 2025
Estimated completion6 June 2025
Sites1 location across Canada

Drugs / interventions tested

Conditions studied

Sponsor

University Health Network, Toronto

Who can join

18 and older, female only, with Ovarian Cancer or Fallopian Tube Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this research study is to see how useful it is to look at biomarkers in the blood and tumor tissue of participants with ovarian, fallopian tube or primary peritoneal cancer who have previously received treatment with a drug called a PARP inhibitor, and using the results to determine the best treatment for these participants. Biomarkers are molecules such as genes (molecules that contain instructions for the development and function of cells in the body) and proteins that may be used to see how well a body responds to certain treatments.

Publications & conference data

6 peer-reviewed publications reference this trial (live from Europe PMC):

  1. PARP inhibitors as single agents and in combination therapy: the most promising treatment strategies in clinical trials for BRCA-mutant ovarian and triple-negative breast cancers.
    Luo L, Keyomarsi K. · · 2022 · cited 56× · PMID 35435784 · DOI 10.1080/13543784.2022.2067527
  2. The potential of PARP inhibitors in targeted cancer therapy and immunotherapy.
    Hunia J, Gawalski K, Szredzka A, Suskiewicz MJ, et al · · 2022 · cited 25× · PMID 36533080 · DOI 10.3389/fmolb.2022.1073797
  3. Immunotherapy for Peritoneal Carcinomatosis: Challenges and Prospective Outcomes.
    Ornella MSC, Badrinath N, Kim KA, Kim JH, et al · · 2023 · cited 24× · PMID 37190310 · DOI 10.3390/cancers15082383
  4. Genome instability and crosstalk with the immune response.
    Chabanon RM, Danlos FX, Ouali K, Postel-Vinay S. · · 2025 · cited 4× · PMID 41188872 · DOI 10.1186/s13073-025-01509-6
  5. Therapeutic Targeting of DNA Damage Repair in the Era of Precision Oncology and Immune Checkpoint Inhibitors.
    Clark CA, Yang ES. · · 2023 · cited 4× · PMID 36751656 · DOI 10.36401/jipo-22-15
  6. Opportunities for predictive proteogenomic biomarkers of drug treatment sensitivity in epithelial ovarian cancer.
    Philips TJ, Erickson BK, Thomas SN. · · 2024 · cited 1× · PMID 39839766 · DOI 10.3389/fonc.2024.1503107

Verify or expand the search:

Other trials of Niraparib

Trials testing the same drug.

Other recruiting trials for Ovarian Cancer

Currently open trials in the same condition.

Other University Health Network, Toronto trials

Trials by the same sponsor.

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Data sources for this page

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