Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
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 Oct 21, 2026, 1:07 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

Brief summary

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

This trial is designed to assess the safety and efficacy of flibanserin in the treatment of premenopausal women with Hypoactive Sexual Desire Disorder (HSDD) that meets standard diagnostic criteria. Efficacy for flibanserin will be assessed vs. a parallel placebo group.

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

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
Jul 2006 (Type not available)
Primary completion
Apr 2008 (Actual)
Completion
Apr 2008 (Actual)
Last update posted
Jun 27, 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 27, 2016 · Synced Oct 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00360529 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →