Accession Number : AD1049019

Title :   A Pharmacokinetic/Pharmacodynamic Study of the Glucocorticoid Receptor Antagonist Mifepristone Combined with Enzalutamide in Castrate-Resistant Prostate Cancer

Descriptive Note : Technical Report,01 Dec 2016,30 Nov 2017

Corporate Author : The University of Chicago Chicago United States

Personal Author(s) : Szmulewitz,Russell

Full Text :

Report Date : 01 Dec 2017

Pagination or Media Count : 13

Abstract : This is a Clinical Exploration Award funding a clinical trial for patients with metastatic, castration resistant prostate cancer (CRPC). For patients with metastatic CRPC, there are few established therapeutic options and the prognosis remains dire. The overarching goal of this award is to build on concept that under the selective pressure of androgen receptor (AR) targeted therapies, prostate cancer adapts. One way it adapts is by upregulating another hormone receptor, the glucocorticoid receptor (GR), which may compensate for diminished AR activity. The clinical trial within this award is a phase I/II clinical trial of the GR antagonist mifepristone in combination with the FDA-approved AR antagonist enzalutamide. The first objective is, within the context of a phase I clinical trial, to establish safe and pharmacologically active doses of the two drugs for use in combination for daily dosing. The second objective is to use pharmacodynamic biomarkers to support the hypothesis that GR antagonism in combination with AR antagonism will delay CRPC progression. During this funding period, two additional sites have opened the study and are now actively recruiting. This has greatly facilitated accrual. Thus far the combination of mifepristone and enzalutamide has been well tolerated with no dose limiting toxicities. During the next year, the goal is to complete enrollment for the phase II trial.

Descriptors :   prostate cancer , androgens , drugs , Pharmacokinetics , biological markers , clinical trials , antigens

Subject Categories : Medicine and Medical Research

Distribution Statement : APPROVED FOR PUBLIC RELEASE