drugset / Trial / NCT02422615

Study of Efficacy and Safety of LEE011 in Men and Postmenopausal Women With Advanced Breast Cancer.

NCT02422615 ↗

Phase 3 Completed 726 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The main aim of this study was to evaluate the efficacy and safety of adding ribociclib to fulvestrant in men and postmenopausal women with hormone receptor positive (HR+), HER2-negative advanced breast cancer.

Timeline

Start
2015-06-09
Primary completion
2017-11-03
Completion
2023-01-11

Outcome

Met primary endpoint

registry analysis (superiority test); Ribociclib + Fulvestrant vs Placebo + Fulvestrant; p = 0.00000041; Cox Proportional Hazard 0.593 (95% CI 0.480 to 0.732); Log Rank NCT02422615 ↗

paper Median progression-free survival was significantly improved with ribociclib plus fulvestrant versus placebo plus fulvestrant PMID 29860922 ↗

release “MONALEESA-3 showed Kisqali plus fulvestrant significantly prolonged progression-free survival (PFS) compared to fulvestrant alone in postmenopausal women” novartis.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ribociclib Small molecule 600 mg Oral
Background Fulvestrant Small molecule 500 mg Intramuscular

Indications