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A Pharmacokinetic (PK) Study to Compare the Absorption of Two Formulations of Transdermal Testosterone Spray and Intrinsa®

Hypoactive Sexual Desire Disorder Clinical Trial

Official title:
A Phase 1, Open-label, Randomized, Three-cohort, Two-period Crossover Study to Determine the Relative Bioavailability of Testosterone Following Application of Two Testosterone Transdermal Spray (TTS) Formulations Once Daily and Intrinsa® Patch Twice Weekly in Healthy, Surgically and Naturally Post-menopausal Women Receiving Estrogen Replacement Therapy

Clinical Trial Summary

The purpose of this study is to determine if the absorption of the testosterone spray is the same as the Intrinsa® Patch.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

  • Hypoactive Sexual Desire Disorder
  • Sexual Dysfunctions, Psychological
Clinical Trial Details
NCT number NCT01096329
Study type Interventional
Source VIVUS, Inc.
Contact
Status Terminated
Phase Phase 1
Start date February 2010
View Details
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