Open-label, Randomized, Cross-over Study to Investigate the Bioequivalence of Estradiol Valerate (EV) and Levomefolate Calcium After Single Oral Administration of a Tablet Formulation Containing 3 mg EV Without and With 0.451 mg Levomefolate Calcium and a Tablet Formulation Containing 0.451 mg Levomefolate Calcium in 42 Healthy Postmenopausal Women.

Trial Profile

Open-label, Randomized, Cross-over Study to Investigate the Bioequivalence of Estradiol Valerate (EV) and Levomefolate Calcium After Single Oral Administration of a Tablet Formulation Containing 3 mg EV Without and With 0.451 mg Levomefolate Calcium and a Tablet Formulation Containing 0.451 mg Levomefolate Calcium in 42 Healthy Postmenopausal Women.

Completed
Phase of Trial: Phase I

Latest Information Update: 21 Apr 2014

At a glance

  • Drugs Estradiol valerate/levomefolic acid (Primary) ; Estradiol valerate; Levomefolic acid
  • Indications Pregnancy
  • Focus Pharmacokinetics
  • Sponsors Bayer
  • Most Recent Events

    • 13 Mar 2010 Status changed from recruiting to completed as reported by ClinicalTrials.gov.
    • 28 Dec 2009 New trial record
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