drugset / Trial / NCT05619913

EPOCH: Eribulin and Pembrolizumab in Ovarian/Uterine Carcinosarcoma

NCT05619913

RandomizedParallel-groupOpen-labelTreatment

Summary

The EPOCH study population is patients with tubo-ovarian carcinosarcoma or uterine carcinosarcoma with evidence of recurrence or progression. The study aims to determine the activity of eribulin as a single agent and the combination of eribulin and pembrolizumab as measured by clinical benefit rate (CBR) at 12 weeks. Additionally, the study aims to establish whether high mobility group A2 (HMGA2) protein expression is a good functional biomarker to predict response to eribulin and pembrolizumab.

Timeline

Start
2023-05-22
Primary completion
2025-03
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Eribulin Small molecule
Subject Pembrolizumab Monoclonal antibody