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An open-label, single-dose, randomized, 2-period, crossover, bioequivalence study to compare levonorgestrel 90 mg/ethinyl estradiol 20 mg in 2 dosage forms with different dissolution characteristics in healthy, cycling women

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Trial Profile

An open-label, single-dose, randomized, 2-period, crossover, bioequivalence study to compare levonorgestrel 90 mg/ethinyl estradiol 20 mg in 2 dosage forms with different dissolution characteristics in healthy, cycling women

Status: Withdrawn prior to enrolment
Phase of Trial: Phase I

Latest Information Update: 10 Nov 2021

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At a glance

  • Drugs Ethinylestradiol/levonorgestrel (Primary)
  • Indications Pregnancy
  • Focus Pharmacokinetics
  • Sponsors Wyeth

    • Most Recent Events

    • 21 Jul 2009 Status changed from not yet recruiting to withdrawn prior to recruitment as reported by ClinicalTrials.gov.
    • 05 May 2007 New trial record.

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