drugset / Trial / NCT02003924

Safety and Efficacy Study of Enzalutamide in Patients With Nonmetastatic Castration-Resistant Prostate Cancer

NCT02003924 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the safety and efficacy of enzalutamide in patients with non metastatic prostate cancer.

Timeline

Start
2013-10-31
Primary completion
2017-06-28
Completion
2025-11-28

Outcome

Met primary endpoint

registry MEDIAN Enzalutamide 160 mg: 36.6 (33.1 to NA) months NCT02003924 ↗

registry analysis (superiority test); Enzalutamide 160 mg vs Placebo; p <0.0001; Hazard Ratio (HR) 0.292 (95% CI 0.241 to 0.352) NCT02003924 ↗

release “In the PROSPER trial, treatment with enzalutamide plus ADT delayed the development of metastases compared to standard of care ADT alone” astellas.com ↗

release “met its primary endpoint of improved metastasis-free survival (MFS)” astellas.com ↗

release “The PROSPER trial evaluated XTANDI plus androgen deprivation therapy (ADT) versus ADT alone in 1,401 patients with non-metastatic CRPC. The study met its primary endpoint” astellas.com ↗

release “PROSPER trial, which demonstrated that the use of XTANDI plus androgen deprivation therapy (ADT) significantly reduced the risk of developing metastasis or death” astellas.com ↗

release “PROSPER met its primary endpoint of metastasis-free survival (MFS), with a median MFS of 36.6 months for men who received enzalutamide plus ADT” astellas.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Enzalutamide Other / unclassified 160 mg Oral