← Eichor
Study identifier: NCT05551208 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Fluzoparib Combined With Bevacizumab in PSROC Previously Treated With PARPi

Condition: Ovarian Cancer  ·  Sponsor: Chongqing University Cancer Hospital

PhasePhase 2
Planned participants42
Who can joinFemale, 18 Years to 75 Years
Healthy volunteersNo

About this study

There are more and more PARPi(PARP inhibitors) resistance for ovarian cancer patients after previous use of PARP inhibitors. Basic studies have found that there is synergistic effect of bevacizumab combined with PARPi. Therefore we designed the study to include 42 ovarian cancer patients who had PARPi for at least half a year and then relapsed (platinum-sensitive, previously 1-3 lines of chemotherapy). After getting complete remission or partial remission with chemotherapy containing platinum and bevacizumab, fluzopanib and bevacizumab were used for maintenance treatment. The progression-free survival, ORR, DCR, DoR, and safety were evaluated based on RECIST V1.1.

This description comes directly from the study's public registry record.

Talk to the study team

Zou Dongling, PH.D.  ·  +8613657690699  ·  cqzl_zdl@163.com

Lin Zhong, M.D.  ·  18623393866  ·  zhonglin1983.12.25@126.com

Always discuss trial participation with your own doctor first.

Locations (1)

Chongqing Cancer HospitalChongqing, Chongqing Municipality, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05551208