CompletedPhase 1ACTRN12605000520639

A Pharmacokinetic Phase I Study to Assess the Effect of Different Application Sites and Formulations, on the Relative Bioavailability and Pharmacokinetics of Estradiol in postmenopausal women from a Metered Dose Transdermal System (MDTS) as hormone replacement therapy.


Sponsor

FemPharm Pty Ltd and/or Acrux DDS Pty Ltd

Enrollment

12 participants

Start Date

Jul 15, 2002

Study Type

Interventional

Conditions


Eligibility

Min Age: -2147483648 YearsMax Age: -2147483648 Years

Plain Language Summary

Simplified for easier understanding

This is an early-phase study looking at: A Pharmacokinetic Phase I Study to Assess the Effect of Different Application Sites and Formulations, on the Relative Bioavailability and Pharmacokinetics of Estradiol in postmenopausal women from a Metered Dose Transdermal System (MDTS) as hormone replacement therapy.. It may be open to adults aged 2147483648 to 2147483648. Please review the full eligibility criteria with your doctor to see if this study is right for you. Participation typically involves medical assessments and follow-up visits as part of the research.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Estradiol MDTS, 7-days, 3-period crossover

Estradiol MDTS, 7-days, 3-period crossover


Locations(1)

Australia

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ACTRN12605000520639