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Completed Phase 3 Interventional Results available

6-mo. Min Eff Dose of Flibanserin: 25 v 50 mg Bid v 50 mg hs v Pbo in Younger Women in NA

ClinicalTrials.gov ID: NCT00360243

Public ClinicalTrials.gov record NCT00360243. 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 Sep 3, 2026, 9:11 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 trial is designed to assess the safety and efficacy of flibanserin in the treatment of premenopausal women with Hypoactive Sexual Desire Disorder (HSDD) that meet standard diagnostic criteria. Efficacy for flibanserin will be assessed vs. a parallel placebo group.

Study identification

NCT ID
NCT00360243
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sprout Pharmaceuticals, Inc
Industry
Enrollment
1,385 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 50 Years
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
81
U.S. states
32
U.S. cities
72
Facility City State ZIP Site status
511.70.01068 Boehringer Ingelheim Investigational Site Huntsville Alabama
511.70.01040 Boehringer Ingelheim Investigational Site Mobile Alabama
511.70.01041 Boehringer Ingelheim Investigational Site Tucson Arizona
511.70.01003 Boehringer Ingelheim Investigational Site Jonesboro Arkansas
511.70.01070 Boehringer Ingelheim Investigational Site Carmichael California
511.70.01026 Boehringer Ingelheim Investigational Site Redding California
511.70.01015 Boehringer Ingelheim Investigational Site San Diego California
511.70.01014 Boehringer Ingelheim Investigational Site Stanford California
511.70.01017 Boehringer Ingelheim Investigational Site Tarzana California
511.70.01072 Boehringer Ingelheim Investigational Site Torrance California
511.70.01078 Boehringer Ingelheim Investigational Site Vista California
511.70.01066 Boehringer Ingelheim Investigational Site Walnut Creek California
511.70.01064 Boehringer Ingelheim Investigational Site Denver Colorado
511.70.01001 Boehringer Ingelheim Investigational Site Wheat Ridge Colorado
511.70.01050 Boehringer Ingelheim Investigational Site Farmington Connecticut
511.70.01006 Boehringer Ingelheim Investigational Site Hartford Connecticut
511.70.01055 Boehringer Ingelheim Investigational Site New London Connecticut
511.70.01024 Boehringer Ingelheim Investigational Site Aventura Florida
511.70.01056 Boehringer Ingelheim Investigational Site Daytona Beach Florida
511.70.01090 Boehringer Ingelheim Investigational Site Fort Lauderdale Florida
511.70.01027 Boehringer Ingelheim Investigational Site Gainesville Florida
511.70.01062 Boehringer Ingelheim Investigational Site New Port Richey Florida
511.70.01043 Boehringer Ingelheim Investigational Site Orlando Florida
511.70.01084 Boehringer Ingelheim Investigational Site Pembroke Pines Florida
511.70.01048 Boehringer Ingelheim Investigational Site St. Petersburg Florida
511.70.01042 Boehringer Ingelheim Investigational Site Stuart Florida
511.70.01063 Boehringer Ingelheim Investigational Site Tampa Florida
511.70.01085 Boehringer Ingelheim Investigational Site Tampa Florida
511.70.01086 Boehringer Ingelheim Investigational Site West Palm Beach Florida
511.70.01022 Boehringer Ingelheim Investigational Site Atlanta Georgia
511.70.01057 Boehringer Ingelheim Investigational Site Atlanta Georgia
511.70.01087 Boehringer Ingelheim Investigational Site Atlanta Georgia
511.70.01052 Boehringer Ingelheim Investigational Site Roswell Georgia
511.70.01060 Boehringer Ingelheim Investigational Site Champaign Illinois
511.70.01058 Boehringer Ingelheim Investigational Site Chicago Illinois
511.70.01032 Boehringer Ingelheim Investigational Site Indianapolis Indiana
511.70.01018 Boehringer Ingelheim Investigational Site Lexington Kentucky
511.70.01007 Boehringer Ingelheim Investigational Site Baton Rouge Louisiana
511.70.01047 Boehringer Ingelheim Investigational Site New Orleans Louisiana
511.70.01079 Boehringer Ingelheim Investigational Site New Orleans Louisiana
511.70.01031 Boehringer Ingelheim Investigational Site Saint Louis Maryland
511.70.01011 Boehringer Ingelheim Investigational Site Haverhill Massachusetts
511.70.01028 Boehringer Ingelheim Investigational Site Detroit Michigan
511.70.01081 Boehringer Ingelheim Investigational Site Detroit Michigan
511.70.01082 Boehringer Ingelheim Investigational Site Billings Montana
511.70.01077 Boehringer Ingelheim Investigational Site Moorestown New Jersey
511.70.01019 Boehringer Ingelheim Investigational Site Endwell New York
511.70.01076 Boehringer Ingelheim Investigational Site New York New York
511.70.01025 Boehringer Ingelheim Investigational Site Poughkeepsie New York
511.70.01067 Boehringer Ingelheim Investigational Site Purchase New York
511.70.01016 Boehringer Ingelheim Investigational Site Mount Airy North Carolina
511.70.01044 Boehringer Ingelheim Investigational Site Raleigh North Carolina
511.70.01049 Boehringer Ingelheim Investigational Site Cincinnati Ohio
511.70.01089 Boehringer Ingelheim Investigational Site Cincinnati Ohio
511.70.01054 Boehringer Ingelheim Investigational Site Columbus Ohio
511.70.01075 Boehringer Ingelheim Investigational Site Dayton Ohio
511.70.01002 Boehringer Ingelheim Investigational Site Mayfield Heights Ohio
511.70.01065 Boehringer Ingelheim Investigational Site Tulsa Oklahoma
511.70.01083 Boehringer Ingelheim Investigational Site Tulsa Oklahoma
511.70.01036 Boehringer Ingelheim Investigational Site Medford Oregon
511.70.01004 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
511.70.01021 Boehringer Ingelheim Investigational Site West Reading Pennsylvania
511.70.01073 Boehringer Ingelheim Investigational Site Warwick Rhode Island
511.70.01023 Boehringer Ingelheim Investigational Site Anderson South Carolina
511.70.01035 Boehringer Ingelheim Investigational Site Charleston South Carolina
511.70.01008 Boehringer Ingelheim Investigational Site Nasville Tennessee
511.70.01020 Boehringer Ingelheim Investigational Site Corpus Christi Texas
511.70.01009 Boehringer Ingelheim Investigational Site Dallas Texas
511.70.01030 Boehringer Ingelheim Investigational Site Houston Texas
511.70.01091 Boehringer Ingelheim Investigational Site Houston Texas
511.70.01013 Boehringer Ingelheim Investigational Site San Antonio Texas
511.70.01005 Boehringer Ingelheim Investigational Site Salt Lake City Utah
511.70.01061 Boehringer Ingelheim Investigational Site Sandy City Utah
511.70.01010 Boehringer Ingelheim Investigational Site Burlington Vermont
511.70.01012 Boehringer Ingelheim Investigational Site Charlottesville Virginia
511.70.01046 Boehringer Ingelheim Investigational Site Norfolk Virginia
511.70.01029 Boehringer Ingelheim Investigational Site Richmond Virginia
511.70.01071 Boehringer Ingelheim Investigational Site Richmond Virginia
511.70.01033 Boehringer Ingelheim Investigational Site Bellevue Washington
511.70.01039 Boehringer Ingelheim Investigational Site Tacoma Washington
511.70.01069 Boehringer Ingelheim Investigational Site Milwaukee Wisconsin

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 NCT00360243, 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 Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00360243 live on ClinicalTrials.gov.

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