drugset / Trial / NCT02107703

A Study of Abemaciclib (LY2835219) Combined With Fulvestrant in Women With Hormone Receptor Positive HER2 Negative Breast Cancer

NCT02107703 ↗

Phase 3 Active not recruiting 669 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

The main purpose of this study is to compare progression-free survival for women with hormone receptor positive (HR+), human epidermal growth factor receptor (HER2) negative advanced breast cancer receiving either abemaciclib + fulvestrant or fulvestrant alone. Participants will be randomized to abemaciclib or placebo in a 2:1 ratio. The study will last about 9 months for each participant. For the endocrine naïve cohort, all participants will received abemaciclib + fulvestrant.

Timeline

Start
2014-07-22
Primary completion
2017-02-14
Completion
2027-12

Outcome

Met primary endpoint

paper Abemaciclib plus fulvestrant significantly extended PFS versus fulvestrant alone (median, 16.4 v 9.3 months; hazard ratio, 0.553; 95% CI, 0.449 to 0.681; P < .001). PMID 28580882 ↗

release “MONARCH 2 trial , which met the study’s primary endpoint of PFS.” astrazeneca.com ↗

release “The MONARCH 2 study previously demonstrated a statistically significant improvement in progression-free survival, the trial's primary endpoint which served as the basis for its approval” lilly.com ↗

release “MONARCH 2 study which had previously demonstrated a statistically significant improvement in the primary endpoint of progression-free survival” lilly.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Abemaciclib Small molecule 150 mg Oral
Background Fulvestrant Small molecule 500 mg Intramuscular

Indications