drugset / Trial / NCT04262089

Neo-adjuvant Pembrolizumab in dMMR/ POLE-EDM Uterine Cancer Patients: a Feasibility Study

NCT04262089 ↗

Non-randomizedParallel-groupOpen-labelTreatment

Summary

In this feasibility study the investigators intend to treat patients with high mutational uterine cancer with two cycles immune checkpoint inhibition before standard-of-care hysterectomy.

Timeline

Start
2020-11-01
Primary completion
2023-04-17
Completion
2023-11-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Pembrolizumab Monoclonal antibody 200 mg Intravenous

Indications