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Completed Phase 3 Interventional Results available

24-week Placebo-controlled Trial of Flibanserin Once Daily in Premenopausal Women With Hypoactive Sexual Desire Disorder

ClinicalTrials.gov ID: NCT00360529

Public ClinicalTrials.gov record NCT00360529. 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 Jul 21, 2026, 7:06 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

A Twenty Four Week, Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Trial of Flibanserin 50mg Every Evening and Flibanserin 100mg Every Evening in Women With Hypoactive Sexual Desire Disorder in North America

Study identification

NCT ID
NCT00360529
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sprout Pharmaceuticals, Inc
Industry
Enrollment
880 participants

Conditions and interventions

Interventions

  • flibanserin Drug

Drug

Eligibility (public fields only)

Age range
18 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
Jun 30, 2006
Primary completion
Mar 31, 2008
Completion
Mar 31, 2008
Last update posted
Jun 26, 2016

2006 – 2008

United States locations

U.S. sites
40
U.S. states
24
U.S. cities
38
Facility City State ZIP Site status
511.71.01034 Boehringer Ingelheim Investigational Site Mobile Alabama
511.71.01042 Boehringer Ingelheim Investigational Site South Birmingham Alabama
511.71.01016 Boehringer Ingelheim Investigational Site Phoenix Arizona
511.71.01041 Boehringer Ingelheim Investigational Site La Mesa California
511.71.01011 Boehringer Ingelheim Investigational Site San Diego California
511.71.01027 Boehringer Ingelheim Investigational Site Westlake Village California
511.71.01035 Boehringer Ingelheim Investigational Site Denver Colorado
511.71.01010 Boehringer Ingelheim Investigational Site Groton Connecticut
511.71.01021 Boehringer Ingelheim Investigational Site New Britain Connecticut
511.71.01037 Boehringer Ingelheim Investigational Site Newark Delaware
511.71.01001 Boehringer Ingelheim Investigational Site Boynton Beach Florida
511.71.01032 Boehringer Ingelheim Investigational Site Clearwater Florida
511.71.01014 Boehringer Ingelheim Investigational Site Miami Florida
511.71.01025 Boehringer Ingelheim Investigational Site Pembroke Pines Florida
511.71.01006 Boehringer Ingelheim Investigational Site Plantation Florida
511.71.01015 Boehringer Ingelheim Investigational Site Atlanta Georgia
511.71.01038 Boehringer Ingelheim Investigational Site Marietta Georgia
511.71.01036 Boehringer Ingelheim Investigational Site Chicago Illinois
511.71.01029 Boehringer Ingelheim Investigational Site Evansville Indiana
511.71.01028 Boehringer Ingelheim Investigational Site Renton Indiana
511.71.01024 Boehringer Ingelheim Investigational Site New Orlean Louisiana
511.71.01040 Boehringer Ingelheim Investigational Site Towson Maryland
511.71.01045 Boehringer Ingelheim Investigational Site Brighton Massachusetts
511.71.01005 Boehringer Ingelheim Investigational Site St Louis Missouri
511.71.01030 Boehringer Ingelheim Investigational Site Albuquerque New Mexico
511.71.01007 Boehringer Ingelheim Investigational Site Rochester New York
511.71.01012 Boehringer Ingelheim Investigational Site The Bronx New York
511.71.01023 Boehringer Ingelheim Investigational Site New Bern North Carolina
511.71.01002 Boehringer Ingelheim Investigational Site Cincinnati Ohio
511.71.01044 Boehringer Ingelheim Investigational Site Cincinnati Ohio
511.71.01026 Boehringer Ingelheim Investigational Site Columbus Ohio
511.71.01039 Boehringer Ingelheim Investigational Site Edmond Oklahoma
511.71.01003 Boehringer Ingelheim Investigational Site Danville Pennsylvania
511.71.01033 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
511.71.01031 Boehringer Ingelheim Investigational Site Pittsburgh Pennsylvania
511.71.01022 Boehringer Ingelheim Investigational Site Mt. Pleasant South Carolina
511.71.01020 Boehringer Ingelheim Investigational Site Germantown Tennessee
511.71.01017 Boehringer Ingelheim Investigational Site San Antonio Texas
511.71.01018 Boehringer Ingelheim Investigational Site San Antonio Texas
511.71.01008 Boehringer Ingelheim Investigational Site Huntington West Virginia

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00360529, 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 Jun 26, 2016 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00360529 live on ClinicalTrials.gov.

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