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Completed Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT03646162

Public ClinicalTrials.gov record NCT03646162. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 1:48 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Randomized, Double-blind, Placebo Controlled, Dose Finding Phase 2 Study Comparing Oral Daily Dosing of VERU-944 to Ameliorate the Vasomotor Symptoms Resulting From ADT in Men With Advanced Prostate Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT03646162
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Veru Inc.
Industry
Enrollment
93 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 13, 2018
Primary completion
Apr 29, 2020
Completion
Oct 14, 2020
Last update posted
Dec 2, 2021

2018 – 2020

United States locations

U.S. sites
24
U.S. states
14
U.S. cities
23
Facility City State ZIP Site status
Gen1 Research Glendale Arizona 85308
Tower Urology Los Angeles California 90048
Urology of San Bernardino San Bernardino California 92404
The Urology Center of Colorado Denver Colorado 80211
Foothills Urology Golden Colorado 80401
Universal Axon Clinical Research Doral Florida 33166
Medical Research Center Miami Florida 33144
North Idaho Urology Coeur d'Alene Idaho 83814
First Urology Jeffersonville Indiana 47130
Regional Urology LLC Shreveport Louisiana 71101
Chesapeake Urology Towson Maryland 21204
Coastal Urology Brick New Jersey 08724
Premier Urology Group Edison New Jersey 08837
Advance Urology Elmont New York 11003
AccuMed Research Garden City New York 11530
Premier Medical Group of the Hudson Valley Poughkeepsie New York 12601
Associated Medical Professionals Syracuse New York 13210
Clinical Research Solutions Middleburg Heights Ohio 44130
Urologic Consultants Bala-Cynwyd Pennsylvania 19004
Mary Crowley Cancer Research Dallas Texas 75230
Urology Clinics of North Texas Dallas Texas 75231
Houston Urology Partners Houston Texas 77091
Urology San Antonio San Antonio Texas 78229
Urology of Virginia Virginia Beach Virginia 23462

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03646162, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 2, 2021 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03646162 live on ClinicalTrials.gov.

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