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Clinical trialNCT00657501CompletedPhase 3Interventional

Safety and Efficacy of LibiGel® for Treatment of Hypoactive Sexual Desire Disorder in Surgically Menopausal Women

SponsorBioSante PharmaceuticalsEnrollment575Hypoactive Sexual Desire Disorder
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This study is a randomized, double-blind, placebo-controlled, multi-center study of the safety and efficacy of LibiGel 300mcg in the treatment of HSDD in surgically menopausal women.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

69 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Canada
  • Biosante Site #175

    Vancouver, British Columbia, Canada

  • Biosante Site #123

    Ottawa, Ontario, Canada

  • Biosante Site #109

    Québec, Quebec, Canada

United States
  • Biosante Site #146

    Mobile, Alabama, United States

  • Biosante Site #171

    Chandler, Arizona, United States

  • Biosante Site #145

    Glendale, Arizona, United States

  • Biosante Site #121

    Phoenix, Arizona, United States

  • Biosante Site #137

    Tucson, Arizona, United States

  • Biosante Site #100

    Jonesboro, Arkansas, United States

  • Biosante Site #155

    Little Rock, Arkansas, United States

  • Biosante Site #221

    Berkely, California, United States

  • Biosante Site #162

    Sacramento, California, United States

  • Biosante Site #112

    San Diego, California, United States

  • Biosante Site #159

    Walnut Creek, California, United States

  • Biosante Site #026

    Lakewood, Colorado, United States

  • Biosante Site #166

    Farmington, Connecticut, United States

  • Biosante Site #132

    New Britain, Connecticut, United States

  • Biosante Site #151

    New London, Connecticut, United States

  • Biosante Site #143

    Jacksonville, Florida, United States

  • Biosante Site #111

    Orlando, Florida, United States

  • Biosante Site #152

    Tampa, Florida, United States

  • Biosante Site #115

    Atlanta, Georgia, United States

  • Biosante Site #141

    Roswell, Georgia, United States

  • Biosante Site #202

    Idaho Falls, Idaho, United States

  • Biosante Site #017

    Meridian, Idaho, United States

  • Biosante Site #156

    Champaign, Illinois, United States

  • Biosante Site #045

    Chicago, Illinois, United States

  • Biosante Site #133

    Chicago, Illinois, United States

  • Biosante Site #149

    Chicago, Illinois, United States

  • Biosante Site #167

    Newburgh, Indiana, United States

  • Biosante Site #163

    Overland Park, Kansas, United States

  • Biosante Site #136

    Lexington, Kentucky, United States

  • Biosante Site #214

    Lexington, Kentucky, United States

  • Biosante Site #157

    Mandeville, Louisiana, United States

  • Biosante Site #110

    Metarie, Louisiana, United States

  • Biosante Site #035

    Ann Arbor, Michigan, United States

  • Biosante Site #124

    Bingham Farms, Michigan, United States

  • Biosante Site #105

    Kalamazoo, Michigan, United States

  • Biosante Site #104

    St Louis, Missouri, United States

  • Biosante Site #127

    Billings, Montana, United States

29 more sites on the registry record.ClinicalTrials.gov ↗

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Placebo gelTestosterone gel
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Mar 2008
Primary completion
30 Sept 2011
Completion
30 Sept 2011
Last update posted
10 Jan 2013
Registered enrollment
575
Registry id
NCT00657501

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.