drugset / Trial / NCT02278120

Study of Efficacy and Safety in Premenopausal Women With Hormone Receptor Positive, HER2-negative Advanced Breast Cancer

NCT02278120 ↗

Phase 3 Completed 672 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study was to determine whether treatment with tamoxifen or a non-steroidal aromatase inhibitors (NSAI) + goserelin + LEE011 prolonged progression-free survival (PFS) compared to treatment with tamoxifen or a NSAI + goserelin + placebo in premenopausal women with hormone receptor positive (HR+), human epidermal growth factor receptor 2 negative (HER2-) advanced breast cancer.

Timeline

Start
2014-11-20
Primary completion
2017-08-21
Completion
2023-04-20

Outcome

Met primary endpoint

registry analysis (superiority test); Ribociclib + NSAI/Tamoxifen + Goserelin vs Placebo + NSAI/Tamoxifen+ Goserelin; p <0.0000001; Hazard Ratio, log 0.553 (95% CI 0.441 to 0.694); Log Rank NCT02278120 ↗

release “The MONALEESA-7 trial met its primary endpoint of progression-free survival (PFS) in premenopausal women” novartis.com ↗

release “Kisqali Phase III MONALEESA-7 trial, in combination with an aromatase inhibitor or tamoxifen and goserelin as initial endocrine-based therapy, showed significantly prolonged progression-free survival” novartis.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ribociclib Small molecule 600 mg —
Background Anastrozole Other / unclassified 1 mg —
Background Goserelin Other / unclassified 3.6 mg —
Background Letrozole Other / unclassified 2.5 mg —
Background Tamoxifen Small molecule 20 mg —

Indications