Clinical Trials Directory

Trials / Unknown

UnknownNCT03684863

Capecitabine in HER-2 Positive Breast Cancer With Pathologic Residual Tumors After Preoperative Chemotherapy

Randomised, Multicenter Phase II Study in Patients With HER-2 Positive Breast Cancer With Capecitabine Versus Observation With Pathologic Residual Tumors After Preoperative Chemotherapy

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Shandong Cancer Hospital and Institute · Academic / Other
Sex
Female
Age
20 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This study is designed to investigate the efficacy and safety of capecitabine, as a postoperative adjuvant chemotherapy, for HER-2 positive breast cancer patients who have pathologic residual cancer cells after the preoperative chemotherapy.

Conditions

Interventions

TypeNameDescription
DRUGCapecitabineobservation

Timeline

Start date
2018-10-01
Primary completion
2023-12-01
Completion
2025-12-01
First posted
2018-09-26
Last updated
2018-09-26

Source: ClinicalTrials.gov record NCT03684863. Inclusion in this directory is not an endorsement.

Capecitabine in HER-2 Positive Breast Cancer With Pathologic Residual Tumors After Preoperative Chemotherapy (NCT03684863) · Clinical Trials Directory