Clinical Trial

Testing the Addition of an Antiangiogenic Drug (Bevacizumab) to Chemotherapy (Carboplatin and Paclitaxel) Combined With Immunotherapy (Pembrolizumab) for pMMR, TP53 Mutated Endometrial Cancer

Recruiting Phase 3
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Summary
This phase III trial compares the effect of bevacizumab in combination with carboplatin, paclitaxel and pembrolizumab to the usual treatments of carboplatin and paclitaxel with or without pembrolizumab in treating patients with stage III, IVA or IVB mismatch repair protein proficient (pMMR) and TP53 mutated endometrial cancer that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) or that has come back after a period of improvement (recurrent). 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. Carboplatin is in a class of medications known as platinum-containing compounds. Carboplatin works by killing, stopping or slowing the growth of tumor cells. Paclitaxel is in a class of medications called antimicrotubule agents. It stops tumor cells from growing and dividing and may kill them. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the tumor, and may interfere with the ability of tumor cells to grow and spread. Adding bevacizumab to the combination of carboplatin, paclitaxel and pembrolizumab may be more effective than the usual treatment combinations of carboplatin and paclitaxel with or without pembrolizumab in treating patients with advanced or recurrent pMMR and TP53 mutated endometrial cancer.
Protocol Amendment History 18 changes
notable Trial sites expanded: 232 -> 242 locations 2026-07-29
notable Trial sites expanded: 223 -> 228 locations 2026-07-07
notable Trial sites expanded: 215 -> 218 locations 2026-06-18
notable Trial sites expanded: 212 -> 215 locations 2026-06-17
notable Trial sites expanded: 206 -> 211 locations 2026-06-12
notable Trial sites expanded: 203 -> 206 locations 2026-06-06
notable Trial sites expanded: 194 -> 203 locations 2026-06-04
notable Trial sites expanded: 170 -> 184 locations 2026-05-14
notable Trial sites expanded: 167 -> 170 locations 2026-05-13
notable Trial sites expanded: 162 -> 165 locations 2026-05-06
notable Trial sites expanded: 147 -> 162 locations 2026-05-05
notable Trial sites expanded: 144 -> 147 locations 2026-05-01
notable Trial sites expanded: 135 -> 144 locations 2026-04-30
notable Trial sites expanded: 112 -> 135 locations 2026-04-28
notable Trial sites expanded: 109 -> 112 locations 2026-04-25
notable Trial sites expanded: 98 -> 108 locations 2026-04-08
notable Trial sites expanded: 91 -> 96 locations 2026-04-02
notable Trial sites expanded: 85 -> 91 locations 2026-03-31
Trial Details
NCT Number NCT07198074
Lead Sponsor National Cancer Institute (NCI)
Conditions Advanced Endometrial Carcinoma, Recurrent Endometrial Carcinoma
Enrollment 255 participants
Start Date 2026-01-27
Primary Completion 2028-07-01 (estimated)
Study Completion 2028-07-01 (estimated)
Updated on ClinicalTrials.gov 2026-08-10