drugset / Trial / NCT06787339

Capecitabine in Low Risk Triple Negative Breast Cancer

NCT06787339 ↗

Phase 2 Not yet recruiting 198 enrolled Fudan University
NaSingle-groupOpen-labelTreatment

Summary

This study aims to evaluate the efficacy and safety of capecitabine as the only adjuvant chemotherapy drug in patients with low-risk early triple-negative breast cancer who have received adequate local treatment. Patients meeting the inclusion criteria will receive capecitabine metronomic therapy for one year.

Timeline

Start
2025-01-15
Primary completion
2028-12-31
Completion
2030-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 650 mg/m2 Oral

Indications