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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 Oct 21, 2026, 1:13 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

Brief summary

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

To estimate the duration of efficacy with continued treatment of double-blind flibanserin or placebo over twenty-four weeks of treatment.

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

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
Jan 2006 (Type not available)
Primary completion
Jul 2007 (Actual)
Completion
Not listed
Last update posted
Mar 16, 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 16, 2012 · 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 NCT00277914 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →