Related Experiment Video
Updated: Dec 24, 2025

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
An FDA Review of Drug Development in Nonmetastatic Castration-resistant Prostate Cancer
Michael Brave1, Chana Weinstock2, Jamie R Brewer2
1Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland. Michael.Brave@fda.hhs.gov.
Abstract:
The FDA has approved three androgen receptor inhibitors-enzalutamide, apalutamide, and darolutamide-for the treatment of patients with nonmetastatic castration-resistant prostate cancer (nmCRPC). These approvals were all based on randomized, double blind, placebo-controlled trials demonstrating large improvements in metastasis-free survival (MFS) and internally consistent evidence of benefit seen across secondary endpoints. In this article, we summarize the FDA regulatory history of MFS and we describe the design, conduct, and results of the three pivotal trials supporting these important treatment options for patients with nmCRPC.
Insights
Three new androgen receptor inhibitors are approved for nonmetastatic castration-resistant prostate cancer (nmCRPC). Pivotal trials showed significant metastasis-free survival (MFS) benefits, supporting these treatments for nmCRPC patients.
Area of Science:
- Oncology
- Pharmacology
- Clinical Trials
Background:
- Nonmetastatic castration-resistant prostate cancer (nmCRPC) is a critical stage requiring effective treatment.
- Androgen receptor inhibitors represent a significant advancement in managing nmCRPC.
- FDA approval signifies robust clinical evidence for new therapeutic options.
Related Concept Videos
Preclinical Development: Overview
Clinical Trials: Overview

