drugset / Trial / NCT02415621

Adaptive Abiraterone Therapy for Metastatic Castration Resistant Prostate Cancer

NCT02415621

Phase 0 Active not recruiting 19 enrolled H. Lee Moffitt Cancer Center and Research Institute
NaSingle-groupOpen-labelTreatment

Summary

Abiraterone is approved in the United States by the U.S. Food and Drug Administration (FDA) to treat metastatic prostate cancer at 1000 mg daily. The purpose of this study is to find out if an on and off schedule of taking abiraterone would prolong the participant's cancer's response to this drug and maintain their functionality to perform their daily activities.

Timeline

Start
2015-04-13
Primary completion
2019-08-12
Completion
2026-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Abiraterone acetate Small molecule 1000 mg Oral

Indications