Clinical trial

Bioequivalence Study Of Bazedoxifene/Conjugated Estrogen Tablets In…

NCT00396799 · Wyeth is now a wholly owned subsidiary of Pfizer, Industry · Completed

Key facts

NCT number NCT00396799
Title Bioequivalence Study Of Bazedoxifene/Conjugated Estrogen Tablets In Postmenopausal Women
Official title An Open-Label, Single-Dose, Randomized-to-Sequence, 2-Period, Crossover, Pivotal Bioequivalence Study Between Bazedoxifene Acetate/Conjugated Estrogens (Premarin Current Process) and Bazedoxifene Acetate/Conjugated Estrogens (Premarin New Process) Tablets Administered to Healthy Postmenopausal Women
Lead sponsor Wyeth is now a wholly owned subsidiary of Pfizer, Industry
Status Completed
Phase Phase 1
Study type Interventional
Conditions Menopause
Intervention type Drug
Interventions bazedoxifene/conjugated estrogens
Start date Nov 1, 2006
Completion Nov 1, 2006
First posted Nov 8, 2006
Last update posted Mar 13, 2007

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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