drugset / Trial / NCT01715285

A Study of Abiraterone Acetate Plus Low-Dose Prednisone Plus Androgen Deprivation Therapy (ADT) Versus ADT Alone in Newly Diagnosed Participants With High-Risk, Metastatic Hormone-Naive Prostate Cancer (mHNPC)

NCT01715285 ↗

Phase 3 Completed 1209 enrolled Janssen Research & Development, LLC
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to determine if newly diagnosed (within previous 3 months) participants with metastatic (spread of cancer cells from one part of the body to another ) hormone-naive prostate cancer (mHNPC) who have high-risk prognostic factors will benefit from the addition of abiraterone acetate plus low-dose prednisone to androgen deprivation therapy (ADT; lutenizing hormone releasing hormone \[LHRH\] agonists or surgical castration).

Timeline

Start
2013-02-12
Primary completion
2016-10-31
Completion
2022-02-13

Outcome

Met primary endpoint

registry analysis (superiority test); Abiraterone Acetate+Prednisone+ADT vs Placebo + ADT; p <0.0001; Hazard Ratio (HR) 0.466 (95% CI 0.394 to 0.550); Log Rank NCT01715285 ↗

registry analysis (superiority test); Abiraterone Acetate+Prednisone+ADT vs Placebo + ADT; p <0.0001; Hazard Ratio (HR) 0.661 (95% CI 0.564 to 0.775); Log Rank NCT01715285 ↗

release “The LATITUDE study showed ZYTIGA® in combination with prednisone and ADT reduced the risk of death by 38 percent compared to placebo plus ADT.” jnj.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Abiraterone acetate Small molecule 1000 mg Oral
Subject Prednisone Other / unclassified 5 mg Oral

Indications