drugset / Trial / NCT00863655

Everolimus in Combination With Exemestane in the Treatment of Postmenopausal Women With Estrogen Receptor Positive Locally Advanced or Metastatic Breast Cancer Who Are Refractory to Letrozole or Anastrozole

NCT00863655 ↗

Phase 3 Completed 724 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

There are no treatments specifically approved after recurrence or progression on a non steroidal aromatase inhibitors (NSAI). In light of the need for new treatment options for postmenopausal women after failure of prior NSAI therapy, the purpose of this Phase III study is to compare efficacy and safety of a treatment with exemestane + everolimus to exemestane + placebo in postmenopausal women with estrogen receptor positive locally advanced or metastatic breast cancer refractory to NSAI.

Timeline

Start
2009-06-03
Primary completion
2014-12-04
Completion
2014-12-04

Outcome

Met primary endpoint

registry MEDIAN Everolimus + Exemestane: 6.93 (6.44 to 8.05) months NCT00863655 ↗

registry p <0.0001; Hazard Ratio (HR) 0.43 (95% CI 0.35 to 0.54); Log Rank NCT00863655 ↗

paper CONCLUSIONS: Everolimus combined with an aromatase inhibitor improved progression-free survival PMID 22149876 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Everolimus Small molecule 10 mg Oral
Background Exemestane Small molecule 25 mg Oral

Indications