Clinical Trial

Comparing UTD2 Combined With Capecitabine to Capecitabine as Adjuvant Therapy for Non-pCR TNBC Patients

Not Yet Recruiting Phase 3
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Summary
Evaluate the IDFS rate, overall survival (OS) rate, and safety profile of UTD2 combined with capecitabine versus capecitabine monotherapy as adjuvant therapy for triple-negative early breast cancer patients who did not achieve pathological complete response (pCR) after neoadjuvant therapy.
Trial Details
NCT Number NCT07021261
Lead Sponsor Fudan University
Conditions Breast Cancer, TNBC
Enrollment 440 participants
Start Date 2025-06-16
Primary Completion 2030-06-16 (estimated)
Study Completion 2032-06-16 (estimated)
Updated on ClinicalTrials.gov 2025-06-13