Last updated on July 2019

Study of VERU-944 to Ameliorate Hot Flashes in Men With Advanced Prostate Cancer


Brief description of study

Randomized, double-blind, placebo controlled, dose finding Phase 2 study comparing oral daily dosing of VERU-944 after a week of loading (daily dosing) with placebo to ameliorate the vasomotor symptoms resulting from androgen deprivation therapy in men with advanced prostate cancer

Detailed Study Description

This study is a multicenter, randomized, double-blind, placebo controlled, dose finding study of VERU-944 to treat hot flashes (vasomotor symptoms) in men with advanced prostate cancer on ADT. The study will have four arms with 30 subjects per arm. The subjects participating in the study will have advanced prostate cancer and will be undergoing androgen deprivation therapy (ADT) with a luteinizing hormone releasing hormone (LHRH) therapy (agonist or antagonist) for at least the three months prior to randomization and be experiencing regular moderate to severe hot flashes while on ADT. Subjects will all continue to receive ADT and will be randomized to receive, for the first four days, a loading dose followed by daily doses of placebo or VERU-944 (10 mg, 50 mg or 100 mg) orally for a total period of 12 weeks.

Clinical Study Identifier: NCT03646162

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Tower Urology

Los Angeles, CA United States
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Urology of San Bernardino

San Bernardino, CA United States
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Foothills Urology

Golden, CO United States
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North Idaho Urology

Coeur d'Alene, ID United States
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First Urology

Jeffersonville, IN United States
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Chesapeake Urology

Towson, MD United States
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Coastal Urology

Brick, NJ United States
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Premier Urology Group

Edison, NJ United States
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Advance Urology

Elmont, NY United States
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AccuMed Research

Garden City, NY United States
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Urologic Consultants

Bala-Cynwyd, PA United States
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Urology San Antonio

San Antonio, TX United States
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Urology of Virginia

Virginia Beach, VA United States
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Gen1 Research

Glendale, AZ United States
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Recruitment Status: Open


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