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Completed Phase 2 Interventional Results available

A Safety and Efficacy Study of Setipiprant Tablets in Androgenetic Alopecia in Males

ClinicalTrials.gov ID: NCT02781311

Public ClinicalTrials.gov record NCT02781311. 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 Oct 21, 2026, 7:44 AM EDT

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

Official title

Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 2A Study of Setipiprant Tablets in Androgenetic Alopecia in Males

Brief summary

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

This study will evaluate the safety, tolerability and efficacy of the oral administration of setipiprant tablets 1000 mg twice daily (BID) relative to placebo in 18 to 49 years old males with androgenetic alopecia (AGA).

Study identification

NCT ID
NCT02781311
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Allergan
Industry
Enrollment
169 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 49 Years
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
Jul 14, 2016 (Actual)
Primary completion
Mar 15, 2018 (Actual)
Completion
May 22, 2018 (Actual)
Last update posted
Apr 5, 2019

2016 – 2018

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Burke Pharmaceutical Research Hot Springs Arkansas 71913 —
Petrus Center for Aesthetic Surgery & Hair Transplantation Little Rock Arkansas 72205 —
Therapeutics Clinical Research San Diego California 92123 —
Radiant Research, Inc. Santa Rosa California 95405 —
DeNova Research Chicago Illinois 60611 —
Heartland Research Associates, LLC Wichita Kansas 67207 —
Michigan Center for Skin Care Research Clinton Township Michigan 48038 —
Minnesota Clinical Study Center Fridley Minnesota 55432 —
University of Minnesota Department of Dermatology Division of Clinical research Minneapolis Minnesota 55455 —
Wake Forest University Health Sciences Department of Dermatology Medical Center Boulevard Winston-Salem North Carolina 27157 —
Cleveland Clinic, Dept of Dermatology Cleveland Ohio 44195 —
NW Dermatology and Research Center Portland Oregon 97210 —
Oregon Medical Research Center Portland Oregon 97223 —
Penn State Hershey Medical Center Dermatology Research Office Hershey Pennsylvania 17033 —
Radiant Research, Inc. Greer South Carolina 29650 —
DermResearch, Inc Austin Texas 78759 —
Suzzane Bruce and Associates P.A., The Center for Skin Research Katy Texas 77494 —
The Education & Research Foundation, Inc Lynchburg Virginia 24501 —

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 NCT02781311, 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 Apr 5, 2019 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02781311 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →