CI

At a glance

ClinicalIndex Comparison Record
Phase 3Recruiting· 880 target
Drug / intervention
Bevacizumab +4 morebiological
Likely dose
Not stated in record
Key inclusion· 14
  • Newly diagnosed, pathologically confirmed FIGO stage III or IV ovarian cancer
  • High grade serous, high grade endometrioid, or other epithelial ovarian cancer with BRCA1/2 deleterious alteration
  • Ovarian, fallopian, or primary peritoneal cancer
  • BRCA1/2 pathogenic/suspected pathogenic variant (germline or somatic)
Key exclusion· 8
  • Previous PARP inhibitor treatment (olaparib, niraparib, rucaparib)
  • Active infection requiring parenteral antibiotics
  • Intra-abdominal abscess, abdominal/pelvic fistula, GI perforation, GI obstruction, or need for NG/gastrostomy tube
  • Unable to swallow oral medication

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06580314
NCT06580314Phase 3RecruitingHigh MomentumUpdated 3mo ago

A Phase III Trial of One vs. Two Years of Maintenance Olaparib, With or Without Bevacizumab, in Patients With BRCA1/2 Mutated or Homologous Recombination Deficient (HRD+) Ovarian Cancer Following Response to First Line Platinum-Based Chemotherapy

NRG Oncology·interventional·Posted Aug 30, 2024·Updated Mar 24, 2026

In Brief

A Phase 3 clinical trial evaluating Bevacizumab, Biospecimen Collection, and 3 other interventions for Fallopian Tube Endometrioid Adenocarcinoma and 8 related conditions. Currently recruiting, targeting 880 participants across 676 sites in 3 countries.

Signals

Enrolling ahead of pace

Detailed Summary

This phase III trial compares the effect of olaparib for one year versus two years, with or without bevacizumab, for the treatment of BRCA 1/2 mutated or homologous recombination deficient stage III or IV ovarian cancer. Olaparib is a polyadenosine 5'-diphosphoribose polymerase (PARP) enzyme inhibitor and may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Bevacizumab is in a class of medications called antiangiogenic agents. It works by stopping the formation of blood vessels that bring oxygen and nutrients to tumor. This may slow the growth and spread of tumor. Giving olaparib for one year with or without bevacizumab may be effective in treating patients with BRCA 1/2 mutated or homologous recombination deficient stage III or IV ovarian cancer, when compared to two years of olaparib.

Study Details

Timeline

Phase 3Recruiting
20252026202720282029203020312032203320342035
First PostedAug 30, 2024
Enrollment StartMar 12, 2025
Primary CompletionDec 31, 2034
TodayJul 2, 2026
Enrollment to primary: 9.8 yearsPosted 1.8 years agoPrimary completion in 8.5 years

Interventions

Bevacizumabbiological

Given IV

Biospecimen Collectionprocedure

Undergo blood sample collection

Computed Tomographyprocedure

Undergo CT

Magnetic Resonance Imagingprocedure

Undergo MRI

Olaparibdrug

Given PO