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Terminated Phase 2 Interventional

Safety and Efficacy Study of AR08 for the Treatment of Vasomotor Symptoms (VMS)

ClinicalTrials.gov ID: NCT02049164

Public ClinicalTrials.gov record NCT02049164. 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 Nov 4, 2026, 2:52 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Placebo-controlled, Forced Titration, Dose-ranging Study of AR08 in the Treatment of Vasomotor Symptoms (VMS) in Menopausal Females: A Proof-of-Concept Study

Brief summary

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

The purpose of this study is to determine the effective dose or dose range of AR08 in the treatment of VMS in menopausal females.

Study identification

NCT ID
NCT02049164
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Arbor Pharmaceuticals, Inc.
Industry
Enrollment
32 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
41 Years and older
Sex
Female
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
Jan 2014 (Type not available)
Primary completion
May 2014 (Actual)
Completion
May 2014 (Actual)
Last update posted
Dec 9, 2015

2014

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Genesis Center for Clinical Research San Diego California 92103 —
Clinical Research Advantage, Inc. Colorado Springs Colorado 80906 —
Blue Skies Center for Women Colorado Springs Colorado 80910 —
Altus Research Lakeworth Florida 99461 —
OB-GYN Associates of Mid-Florida, P.A. Leesburg Florida 34748 —
Comprehensive Clinical Trials, LLC West Palm Beach Florida 33409 —
Cypress Medical Research Center Wichita Kansas 67226 —
Clinical Research Center of Nevada Las Vegas Nevada 89123 —
Lawrence OB/Gyn Associates Lawrenceville New Jersey 08648 —
Hawthorne Medical Research, Inc. Winston-Salem North Carolina 27103 —
Clinical Research of Philadelphia, LLC Philadelphia Pennsylvania 19114 —
Chattanooga Medical Research, LLC Chattanooga Tennessee 37404 —
TMC Life Research, Inc. Houston Texas 77054 —
Tidewater Physicians for Women Norfolk Virginia 23502 —
Seattle Womens: Health, Research, Gynecology Seattle Washington 98105 —

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 NCT02049164, 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 9, 2015 · Synced Nov 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02049164 live on ClinicalTrials.gov.

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