Clinical Trial

Clinical Trial of Neoadjuvant Chemotherapy With Atezolizumab or Placebo in Patients With Triple-Negative Breast Cancer Followed After Surgery by Atezolizumab or Placebo

Active, Not Recruiting Phase 3
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Record status
This record was last updated April 8, 2024 (before its estimated December 31, 2024 completion). Its status may not reflect the trial's current state.
Summary
The main purpose of this study is to learn if the usual chemotherapy given before surgery (neoadjuvant therapy) for breast cancer plus the experimental drug, atezolizumab, is better than the usual chemotherapy plus a placebo. (A placebo is a drug that looks like the study drug but contains no medication.) The usual chemotherapy in this study is paclitaxel (WP) and carboplatin followed by doxorubicin and cyclophosphamide (AC) or epirubicin and cyclophosphamide (EC). Usually, after neoadjuvant therapy and surgery for triple negative breast cancer, no additional treatment is given unless the cancer returns. This study will also look at continuing treatment after surgery with atezolizumab or the placebo. To be better, atezolizumab given with the neoadjuvant therapy should be better at: 1) decreasing the amount of tumor in the breast than the placebo given with the usual chemotherapy and 2) decreasing the chance of the cancer from returning after surgery. Another purpose of this study is to test the good and bad effects of atezolizumab when added to the usual chemotherapy. Atezolizumab may keep your cancer from growing but it can also cause side effects.
Protocol Amendment History 26 amendments
This ClinicalTrials.gov record has been amended 26 times since 2017-09-11; most recent amendment 2024-04-04.
Status change: Recruiting → Active, Not Recruiting 2021-10-04
Status change: Not Yet Recruiting → Recruiting 2017-12-20
Trial Details
NCT Number NCT03281954
Lead Sponsor NSABP Foundation Inc
Collaborators: Genentech, Inc., Hoffmann-La Roche
Conditions Triple Negative Breast Cancer
Enrollment 1,550 participants
Start Date 2017-12-19
Primary Completion 2024-12-31 (estimated)
Study Completion 2027-11-30 (estimated)
Updated on ClinicalTrials.gov 2024-04-08