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A Study to Evaluate the Efficacy/Safety of Transdermal Testosterone for 52 Weeks and Safety for 52 Weeks in Naturally Menopausal Women With Hypoactive Sexual Desire Disorder on Oral Hormone Replacement Therapy.

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Trial Profile

A Study to Evaluate the Efficacy/Safety of Transdermal Testosterone for 52 Weeks and Safety for 52 Weeks in Naturally Menopausal Women With Hypoactive Sexual Desire Disorder on Oral Hormone Replacement Therapy.

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 01 Apr 2010

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At a glance

  • Drugs Testosterone (Primary)
  • Indications Decreased libido
  • Focus Therapeutic Use
  • Sponsors Procter & Gamble

Most Recent Events

  • 30 Mar 2010 Warner Chilcott added as trial sponsor and trial affiliate as reported by ClinicalTrials.gov.
  • 20 Oct 2009 Additional lead trial investigator identified as reported by ClinicalTrials.gov.
  • 14 Feb 2008 The expected completion date for this trial is now 1 Jul 2006.

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