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)
View Full Details on ANZCTR
For the most up-to-date information, visit the official listing.
ACTRN12605000520639