drugset / Trial / NCT06040970

Sacituzumab Govitecan in Combination With Cisplatin in Platinum Sensitive Recurrent Ovarian and Endometrial Cancer

NCT06040970

Phase 1/2 Recruiting 54 enrolled Icahn School of Medicine at Mount Sinai
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is an open-label, Phase 1 study with a dose expansion cohort of Sacituzumab Govitecan in Combination with Cisplatin in Platinum Sensitive Recurrent Ovarian and Endometrial Cancer. The goal of the study is to determine the optimal dose of sacituzumab govitecan for use in combination with cisplatin for treatment of epithelial ovarian and endometrial cancers.

Timeline

Start
2024-10-23
Primary completion
2026-07-01
Completion
2027-07-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Sacituzumab Monoclonal antibody 5 mg/kg Intravenous
Subject Sacituzumab Monoclonal antibody 7.5 mg/kg Intravenous
Background Cisplatin Other / unclassified 70 mg/m2 Intravenous