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Clinical trialNCT00613002CompletedPhase 3Interventional

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

SponsorBioSante PharmaceuticalsEnrollment597Hypoactive 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

63 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 #188

    Sarnia, Ontario, Canada

  • Biosante Site #054

    Windsor, Ontario, Canada

  • Biosante Site #193

    Shawinigan, Quebec, Canada

United States
  • Biosante Site #215

    Birmingham, Alabama, United States

  • Biosante Site #095

    Hoover, Alabama, United States

  • Biosante Site #014

    Huntsville, Alabama, United States

  • Biosante Site #027

    Glendale, Arizona, United States

  • Biosante Site #040

    Tucson, Arizona, United States

  • Biosante Site #052

    Hot Springs, Arkansas, United States

  • Biosante Site #182

    Buena Park, California, United States

  • Biosante Site #008

    San Diego, California, United States

  • Biosante Site #007

    Denver, Colorado, United States

  • Biosante Site #216

    Denver, Colorado, United States

  • Biosante Site #036

    Ridgefield, Connecticut, United States

  • Biosante Site #013

    Washington D.C., District of Columbia, United States

  • Biosante Site #024

    Miami, Florida, United States

  • Biosante Site #219

    Pinellas Park, Florida, United States

  • Biosante Site #041

    St. Petersburg, Florida, United States

  • Biosante Site #009

    West Palm Beach, Florida, United States

  • Biosante Site #189

    Addison, Illinois, United States

  • Biosante Site #005

    Shreveport, Louisiana, United States

  • Biosante Site #004

    Baltimore, Maryland, United States

  • Biosante Site #044

    Detroit, Michigan, United States

  • Biosante Site #047

    Grand Rapids, Michigan, United States

  • Biosante Site #033

    Saginaw, Michigan, United States

  • Biosante Site #031

    Saint Clair Shores, Michigan, United States

  • Biosante Site #208

    Edina, Minnesota, United States

  • Biosante Site #198

    Saint Paul, Minnesota, United States

  • Biosante Site #051

    Missoula, Montana, United States

  • Biosante Site #006

    Lincoln, Nebraska, United States

  • Biosante Site #217

    Las Vegas, Nevada, United States

  • Biosante Site #015

    Poughkeepsie, New York, United States

  • Biosante Site #059

    Cary, North Carolina, United States

  • Biosante Site #079

    Charlotte, North Carolina, United States

  • Biosante Site #061

    Winston-Salem, North Carolina, United States

  • Biosante Site #056

    Fargo, North Dakota, United States

  • Biosante Site #210

    Akron, Ohio, United States

  • Biosante Site #212

    Cincinnati, Ohio, United States

  • Biosante Site #213

    Columbus, Ohio, United States

  • Biosante Site #050

    Eugene, Oregon, United States

23 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 Dec 2006
Primary completion
30 Sept 2011
Completion
30 Sept 2011
Last update posted
10 Jan 2013
Registered enrollment
597
Registry id
NCT00613002

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.