Actively Recruiting

Phase 2
Phase 3
Age: 18Years - 75Years
FEMALE
NCT07472140

PARP (Poly (ADP-ribose) Polymerase) Inhibitor With or Without Angiogenesis Inhibitor in Homologous Recombination Deficient Primary Ovarian Cancer, Fallopian-Tube Cancer, or Primary Peritoneal Cancer

Led by N.N. Alexandrov National Cancer Centre · Updated on 2026-03-16

120

Participants Needed

1

Research Sites

417 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a randomized trial evaluating the results of using of PARP inhibitor combined with angiogenesis inhibitor. in patients with homologous recombination deficient primary ovarian cancer, fallopian-tube cancer, or primary peritoneal cancer of the III-IV stages.

CONDITIONS

Official Title

PARP (Poly (ADP-ribose) Polymerase) Inhibitor With or Without Angiogenesis Inhibitor in Homologous Recombination Deficient Primary Ovarian Cancer, Fallopian-Tube Cancer, or Primary Peritoneal Cancer

Who Can Participate

Age: 18Years - 75Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18-75 years
  • Histologically confirmed serous or endometrioid high-grade ovarian cancer, fallopian-tube cancer, or primary peritoneal cancer
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Ability to undergo diagnostic laparoscopy or cytoreductive surgery
  • Presence of homologous recombination deficiency (HRD)
  • No contraindications to chemotherapy or bevacizumab
  • Signed informed consent to participate in the study
Not Eligible

You will not qualify if you...

  • Presence of another active malignant invasive cancer
  • Pregnancy or lactation
  • Disease progression during treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

N.N. Alexandrov National Caner Centre

Minsk, Lesnoy, Belarus, 223040

Actively Recruiting

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Research Team

H

Hanna Trukhan

CONTACT

S

Sergey Mavrichev

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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