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Clinical Trials/ACTRN12605000520639
ACTRN12605000520639
Completed
Phase 1

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.

FemPharm Pty Ltd and/or Acrux DDS Pty Ltd0 sites12 target enrollmentSeptember 26, 2005

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Hormone replacement therapy in post-meonpausal women
Sponsor
FemPharm Pty Ltd and/or Acrux DDS Pty Ltd
Enrollment
12
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 26, 2005
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional

Investigators

Sponsor
FemPharm Pty Ltd and/or Acrux DDS Pty Ltd

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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