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Completed Phase 2 Interventional

Evaluate the Safety and Efficacy of Bremelanotide in Women With Female Sexual Arousal Disorder (FSAD)

ClinicalTrials.gov ID: NCT00425256

Public ClinicalTrials.gov record NCT00425256. 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 24, 2026, 8:17 PM EDT

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

Brief summary

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

This 8 week at home study is designed to explore efficacy endpoints and evaluate the safety of intranasal Bremelanotide in women with Female Sexual Arousal Disorder. Efficacy will be assessed vs. a parallel placebo group.

Study identification

NCT ID
NCT00425256
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Palatin Technologies, Inc
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
21 Years to 70 Years
Sex
Female
Healthy volunteers
Not listed

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

Study timeline

Start date
Feb 2006 (Type not available)
Primary completion
May 2007 (Actual)
Completion
May 2007 (Actual)
Last update posted
Feb 23, 2011

2006 – 2007

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
20
Facility City State ZIP Site status
Medical Affiliated Research Center Huntsville Alabama — —
Quality of Life Medical & Research Center, LLC Tucson Arizona — —
University of California, Department of Family and Preventative Medicine La Jolla California — —
Downtown Women's Health Care Denver Colorado — —
Coastal Connecticut Research New London Connecticut — —
South Florida Medical Research Aventura Florida — —
Clinical Study Center Fort Myers Florida — —
Center For Marital and Sexual Health of South Florida West Palm Beach Florida — —
Northeast Indiana Research Fort Wayne Indiana — —
Center for Sexual Medicine at Sheppard Pratt Baltimore Maryland — —
Advanced Biomedical Research, Inc Hackensack New Jersey — —
The Center for Female Sexuality Purchase New York — —
Wake Research Associates, LLC Raleigh North Carolina — —
Lyndhurst Gynecologic Associates Winston-Salem North Carolina — —
The Ohio State University Columbus Ohio — —
Medford Women's Clinic, LLP Medford Oregon — —
Clinical Trials Research Services, LLC Pittsburgh Pennsylvania — —
Advanced Clinical Therapies, Inc. West Reading Pennsylvania — —
Accelovance Houston Texas — —
Women's Clinical Research Center Seattle Washington — —

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 NCT00425256, 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 Feb 23, 2011 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00425256 live on ClinicalTrials.gov.

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