drugset / Trial / NCT06291064

Trial Studying Chemotherapy in Nigerian Women With Triple Negative Breast Cancer

NCT06291064

Phase 2 Recruiting 85 enrolled University of Chicago
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this study is to determine what proportion of participants will achieve complete pathological response with epirubicin+ cyclophosphamide followed by docetaxel +carboplatin. This will also examine the potential of using signals in the blood (biomarkers) to identify resistance to chemotherapy in Nigerian women with triple negative breast cancer (TNBC). All enrollment to this trial will occur at sites in Nigeria. University of Chicago is serving as coordinating center and will be involved in data analysis.

Timeline

Start
2025-03-18
Primary completion
2029-06
Completion
2032-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule Oral
Subject Carboplatin Small molecule Intravenous
Subject Cyclophosphamide Other / unclassified Intravenous
Subject Docetaxel Small molecule Intravenous
Subject Epirubicin Small molecule Intravenous