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A Randomized, Double-Blind, Placebo-controlled, Multicenter, 52-week Study to Evaluate the Endometrial Safety of Transdermal Testosterone (300 Mcg/Day) in Naturally Postmenopausal Women With Hypoactive Sexual Desire Disorder.

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A Randomized, Double-Blind, Placebo-controlled, Multicenter, 52-week Study to Evaluate the Endometrial Safety of Transdermal Testosterone (300 Mcg/Day) in Naturally Postmenopausal Women With Hypoactive Sexual Desire Disorder.

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 17 Dec 2011

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At a glance

  • Drugs Testosterone (Primary)
  • Indications Female sexual dysfunction
  • Focus Adverse reactions
  • Sponsors Procter & Gamble; Warner Chilcott

    • Most Recent Events

    • 21 Jul 2009 Planned number of patients changed from 1250 to 1271 as reported by ClinicalTrials.gov.
    • 21 Jul 2009 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
    • 17 Jul 2009 Planned end date changed from 1 Dec 2008 to 1 Jan 2009 as reported by ClinicalTrials.gov.

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