Postmenopause Clinical Trial
Official title:
An Open-Label, Single/Multiple Dose Non-Randomized, 3-Period, Crossover Study To Determine The Potential Drug Interaction Of Conjugated Estrogens (CE) On Bazedoxifene In Healthy Postmenopausal Women.
The purpose of this study is to evaluate the pharmacokinetics (absorption, distribution,
breakdown and elimination in the body) of a single dose of bazedoxifene (BZA) 20 mg tablet
when administered together with multiple doses of Premarin (conjugated estrogens or CE) to
healthy postmenopausal women.
Information will also be obtained regarding the safety and tolerability of this combination
in healthy, postmenopausal women.
n/a
Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
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