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Study Comparing Formulations of Bazedoxifene/Conjugated Estrogens

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00550303
Recruitment Status : Completed
First Posted : October 29, 2007
Last Update Posted : December 27, 2007
Information provided by:

October 25, 2007
October 29, 2007
December 27, 2007
October 2007
Not Provided
Same as current
Complete list of historical versions of study NCT00550303 on ClinicalTrials.gov Archive Site
Safety & tolerability
Same as current
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Study Comparing Formulations of Bazedoxifene/Conjugated Estrogens
An Open-Label, Single-Dose, Non-Randomized, 4-Period Crossover Bioavailability Study of Bazedoxifene Contained in Bazedoxifene/Conjugated Estrogen Tablets Administered to Healthy Postmenopausal Women
The primary purpose is to determine bioavailability of Bazedoxifene/conjugated estrogen formulations for future testing purposes.
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Phase 1
Allocation: Non-Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Drug: bazedoxifene/conjugated estrogens combination
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
November 2007
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Inclusion Criteria:

  • Healthy, post menopausal women ages 45 to 70

Exclusion Criteria:

  • Male subjects
Sexes Eligible for Study: Female
45 Years to 70 Years   (Adult, Senior)
Contact information is only displayed when the study is recruiting subjects
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Wyeth is now a wholly owned subsidiary of Pfizer
Not Provided
Study Director: Medical Monitor Wyeth is now a wholly owned subsidiary of Pfizer
Wyeth is now a wholly owned subsidiary of Pfizer
December 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP