drugset / Trial / NCT02319837

Safety and Efficacy Study of Enzalutamide Plus Leuprolide in Patients With Nonmetastatic Prostate Cancer (EMBARK)

NCT02319837 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to assess enzalutamide plus leuprolide in patients with high-risk nonmetastatic prostate cancer progressing after radical prostatectomy or radiotherapy or both. The randomized / blinded portion of the study is now completed following primary endpoint analyses. The study remains ongoing in open label format.

Timeline

Start
2014-12-17
Primary completion
2023-01-31
Completion
2026-09-19

Outcome

Met primary endpoint

registry analysis (other test); Enzalutamide + Leuprolide vs Placebo + Leuprolide; p <0.0001; Hazard Ratio (HR) 0.424 (95% CI 0.296 to 0.607) NCT02319837 ↗

release “EMBARK met its primary endpoint of metastasis-free survival (MFS) for the XTANDI plus leuprolide arm” astellas.com ↗

release “The EMBARK trial primary analysis was previously reported in The New England Journal of Medicine in 2023, demonstrating that the study met its primary endpoint” pfizer.com ↗

release “The MFS results from the EMBARK study demonstrate that this intervention with XTANDI plus leuprolide was statistically significant for patients with high-risk BCR.” astellas.com ↗

release “The EMBARK study met its primary endpoint of metastasis-free survival (MFS) for the XTANDI plus leuprolide arm” astellas.com ↗

release “EMBARK met its primary endpoint of metastasis-free survival (MFS) for the XTANDI plus leuprolide arm” astellas.com ↗

release “The EMBARK trial primary analysis was previously reported in the New England Journal of Medicine in 2023, demonstrating that the study met its primary endpoint” pfizer.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Enzalutamide Other / unclassified 160 mg Oral
Subject Leuprolide Other / unclassified 22.5 mg Intramuscular

Indications