drugset / Trial / NCT04109066

Study of Nivolumab Versus Placebo in Combination With Neoadjuvant Chemotherapy and Adjuvant Endocrine Therapy in Participants With High-risk, Estrogen Receptor-Positive (ER+), Human Epidermal Growth Factor Receptor 2-Negative (HER2-) Primary Breast Cancer

NCT04109066 ↗

Phase 3 Completed 521 enrolled Bristol-Myers Squibb
RandomizedParallel-groupDouble-blindTreatment

Summary

A randomized multi-arm study evaluating the efficacy and safety of nivolumab versus placebo in combination with neoadjuvant (pre-surgery) chemotherapy and adjuvant (post-surgery) endocrine therapy in participants with high-risk, estrogen receptor-positive, human epidermal growth factor receptor 2-negative (ER+, HER2-) early stage breast cancer.

Timeline

Start
2019-11-18
Primary completion
2023-01-16
Completion
2023-12-27

Outcome

Met primary endpoint

paper The primary endpoint of pCR was significantly higher in the nivolumab arm compared with placebo (24.5% versus 13.8%; P = 0.0021), PMID 39838118 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Nivolumab Monoclonal antibody — Intravenous
Background Cyclophosphamide Other / unclassified — —
Background Paclitaxel Small molecule — —

Indications