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An open-label, single-dose, randomized, 3-period, crossover, bioequivalence study between two new formulations of 0.45mg/1.5mg Premarin [conjugated estrogens]/medroxyprogesterone acetate (MPA) compared with a reference formulation of 0.45mg/1.5mg Premarin/MPA (Prempro in healthy postmenopausal women

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Trial Profile

An open-label, single-dose, randomized, 3-period, crossover, bioequivalence study between two new formulations of 0.45mg/1.5mg Premarin [conjugated estrogens]/medroxyprogesterone acetate (MPA) compared with a reference formulation of 0.45mg/1.5mg Premarin/MPA (Prempro in healthy postmenopausal women

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 10 Nov 2021

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At a glance

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

    • Most Recent Events

    • 08 Jun 2007 Status change from, initiated to completed (according to NCT).
    • 16 Oct 2006 New trial record.

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