drugset / Trial / NCT06268327

Adding Adjuvant Cisplatin and Gemicitabine Versus Capecitabine in Triple-negative Breast Cancer Patients in Non pCR After Neoadjuvant Standard Chemotherapy

NCT06268327

Phase 2/3 Not yet recruiting 30 enrolled Assiut University
RandomizedParallel-groupOpen-labelTreatment

Summary

In our study; investigator aim To show efficacy and toxicity of Adjuvant cisplatin and gemcitabine in triple-negative breast cancer patients with non pathologically complete response after neoadjuvant chemotherapy To compare outcome of adjuvant cisplatin and gemcitabine versus capecitabine

Timeline

Start
2024-04-30
Primary completion
2025-10-30
Completion
2026-10-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 1000 mg/m2
Subject Capecitabine Small molecule 1250 mg/m2
Subject Cisplatin Other / unclassified 70 mg/m2
Subject Gemcitabine Small molecule 1000 mg/m2

Indications