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An Open-label, Randomized, Two-period, Two-sequence Crossover Trial to Assess the Bioequivalence of the Liquid Formulation Versus the Freeze-dried Formulation of 900 IU r-hFSH and 450 IU r-hLH in Pergoveris, Administered Subcutaneously in Pituitary Suppressed Healthy Premenopausal Female Subjects

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Trial Profile

An Open-label, Randomized, Two-period, Two-sequence Crossover Trial to Assess the Bioequivalence of the Liquid Formulation Versus the Freeze-dried Formulation of 900 IU r-hFSH and 450 IU r-hLH in Pergoveris, Administered Subcutaneously in Pituitary Suppressed Healthy Premenopausal Female Subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 06 Nov 2021

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At a glance

Most Recent Events

  • 07 Dec 2015 Status changed from recruiting to completed as reported by ClinicalTrials.gov.
  • 12 Aug 2015 Planned End Date changed from 1 Jul 2015 to 1 Feb 2016, according to ClinicalTrials.gov record.
  • 12 Aug 2015 Planned primary completion date changed from 1 Jul 2015 to 1 Oct 2015, according to ClinicalTrials.gov record.

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