An Open-Label, Single-Dose, Randomized, 4-Period, Partial Crossover Bioequivalence/Bioavailability Study Among Four New Formulations of Premarin 0.45 mg/Medroxyprogesterone Acetate (MPA) 1.5 mg Compared With a Reference Formulation of Premarin/MPA (Prempro) 0.45 mg/1.5 mg in Healthy Postmenopausal Women

Trial Profile

An Open-Label, Single-Dose, Randomized, 4-Period, Partial Crossover Bioequivalence/Bioavailability Study Among Four New Formulations of Premarin 0.45 mg/Medroxyprogesterone Acetate (MPA) 1.5 mg Compared With a Reference Formulation of Premarin/MPA (Prempro) 0.45 mg/1.5 mg in Healthy Postmenopausal Women

Completed
Phase of Trial: Phase I

Latest Information Update: 18 Nov 2006

At a glance

  • Drugs Conjugated estrogens/medroxyprogesterone (Primary)
  • Indications Menopausal syndrome
  • Focus Pharmacokinetics
  • Sponsors Wyeth
  • Most Recent Events

    • 18 Nov 2006 New trial record.
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