Phase II Study of Pembrolizumab, Bevacizumab, and Cyclophosphamide for High-Grade Ovarian Cancer

This study is looking at a combination of three drugs for women with high-grade ovarian cancer who still have a small amount of cancer remaining after their initial treatment. The drugs are pembrolizumab (an immunotherapy that helps your immune system fight cancer), bevacizumab (which targets blood vessel growth in tumors), and oral cyclophosphamide. Researchers want to see if this combination can help control the cancer for at least six months and how safe it is. You may be eligible if you are an adult woman (18 or older) with this type of ovarian cancer and meet other health criteria. The study is currently unclear on its recruitment status and plans to enroll 20 participants.

Study design
This is a Phase II interventional study, meaning all participants will receive the study treatment. It aims to enroll 20 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Your safety will be monitored throughout the study, which is expected to last an average of one year.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06083844

Phase II Investigation of Pembrolizumab in Combination With Bevacizumab and Oral Cyclophosphamide in Patients With High Grade Ovarian Cancer and Surgically Documented Minimal Residual Disease After Frontline Therapy

Recruiting
PHASE2Ages 18+InterventionalTreatment
M.D. Anderson Cancer Center
~20 participants
Updated 2026-05-18 on ClinicalTrials.gov
What's tested:PembrolizumabBevacizumabCyclophosphamide

At a glance

Recruiting sites
1 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0
Measured over Through study completion; an average of 1 year.
Ovarian Cancer
2 sites across 2 states
New York1
Texas1
  • Amir Jazaeri, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

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  • Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0Through study completion; an average of 1 year.