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Completed Phase 3 Interventional

Flibanserin Randomized Withdrawal Trial in Pre-menopausal Women

ClinicalTrials.gov ID: NCT00277914

Public ClinicalTrials.gov record NCT00277914. 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 Jun 26, 2026, 11:39 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

12-month Sustained Efficacy of Flibanserin v Placebo n Younger Women With HSDD in NA

Study identification

NCT ID
NCT00277914
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sprout Pharmaceuticals, Inc
Industry
Enrollment
749 participants

Conditions and interventions

Interventions

  • Flibanserin Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 45 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
Dec 31, 2005
Primary completion
Jun 30, 2007
Completion
Not listed
Last update posted
Mar 15, 2012

Started 2006

United States locations

U.S. sites
55
U.S. states
32
U.S. cities
55
Facility City State ZIP Site status
511.74.01051 Boehringer Ingelheim Investigational Site Birmingham Alabama
511.74.01027 Boehringer Ingelheim Investigational Site Mobile Alabama
511.74.01029 Boehringer Ingelheim Investigational Site Scottsdale Arizona
511.74.01031 Boehringer Ingelheim Investigational Site Tucson Arizona
511.74.01004 Boehringer Ingelheim Investigational Site Jonesboro Arkansas
511.74.01053 Boehringer Ingelheim Investigational Site Little Rock Arkansas
511.74.01033 Boehringer Ingelheim Investigational Site Palm Springs California
511.74.01003 Boehringer Ingelheim Investigational Site Palo Alto California
511.74.01015 Boehringer Ingelheim Investigational Site Sacramento California
511.74.01013 Boehringer Ingelheim Investigational Site San Diego California
511.74.01052 Boehringer Ingelheim Investigational Site Torrance California
511.74.01022 Boehringer Ingelheim Investigational Site Aurora Colorado
511.74.01046 Boehringer Ingelheim Investigational Site Denver Colorado
511.74.01002 Boehringer Ingelheim Investigational Site Groton Connecticut
511.74.01023 Boehringer Ingelheim Investigational Site Middlebury Connecticut
511.74.01009 Boehringer Ingelheim Investigational Site West Hartford Connecticut
511.74.01035 Boehringer Ingelheim Investigational Site Newark Delaware
511.74.01039 Boehringer Ingelheim Investigational Site Coral Gables Florida
511.74.01019 Boehringer Ingelheim Investigational Site Gainesville Florida
511.74.01044 Boehringer Ingelheim Investigational Site Hollywood Florida
511.74.01001 Boehringer Ingelheim Investigational Site Hudson Florida
511.74.01043 Boehringer Ingelheim Investigational Site Pembroke Pines Florida
511.74.01032 Boehringer Ingelheim Investigational Site St. Petersburg Florida
511.74.01036 Boehringer Ingelheim Investigational Site Roswell Georgia
511.74.01047 Boehringer Ingelheim Investigational Site Champaign Illinois
511.74.01038 Boehringer Ingelheim Investigational Site Evansville Indiana
511.74.01014 Boehringer Ingelheim Investigational Site Lexington Kentucky
511.74.01007 Boehringer Ingelheim Investigational Site Baton Rouge Louisiana
511.74.01024 Boehringer Ingelheim Investigational Site Rockland Maine
511.74.01030 Boehringer Ingelheim Investigational Site Ann Arbor Michigan
511.74.01056 Boehringer Ingelheim Investigational Site Bingham Farms Michigan
511.74.01010 Boehringer Ingelheim Investigational Site St Louis Missouri
511.74.01012 Boehringer Ingelheim Investigational Site Billings Montana
511.74.01045 Boehringer Ingelheim Investigational Site Omaha Nebraska
511.74.01041 Boehringer Ingelheim Investigational Site Las Vegas Nevada
511.74.01055 Boehringer Ingelheim Investigational Site Reno Nevada
511.74.01018 Boehringer Ingelheim Investigational Site Poughkeepsie New York
511.74.01011 Boehringer Ingelheim Investigational Site Rochester New York
511.74.01048 Boehringer Ingelheim Investigational Site Winston-Salem North Carolina
511.74.01021 Boehringer Ingelheim Investigational Site Cincinnati Ohio
511.74.01042 Boehringer Ingelheim Investigational Site Columbus Ohio
511.74.01050 Boehringer Ingelheim Investigational Site Edmond Oklahoma
511.74.01006 Boehringer Ingelheim Investigational Site Eugene Oregon
511.74.01034 Boehringer Ingelheim Investigational Site Medford Oregon
511.74.01040 Boehringer Ingelheim Investigational Site Pittsburgh Pennsylvania
511.74.01017 Boehringer Ingelheim Investigational Site Anderson South Carolina
511.74.01057 Boehringer Ingelheim Investigational Site Knoxville Tennessee
511.74.01008 Boehringer Ingelheim Investigational Site Nashville Tennessee
511.74.01016 Boehringer Ingelheim Investigational Site Plano Texas
511.74.01020 Boehringer Ingelheim Investigational Site San Antonio Texas
511.74.01005 Boehringer Ingelheim Investigational Site Salt Lake City Utah
511.74.01026 Boehringer Ingelheim Investigational Site Norfolk Virginia
511.74.01037 Boehringer Ingelheim Investigational Site Renton Washington
511.74.01028 Boehringer Ingelheim Investigational Site Spokane Washington
511.74.01049 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00277914, 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 Mar 15, 2012 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00277914 live on ClinicalTrials.gov.

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