Trial Profile

A Phase 1, Open Label, Single Dose, Parallel-group Study to Investigate the Pharmacokinetics of the Fixed Combination of 900 IU r-hFSH and 450 IU r-hLH Given as Pergoveris®, Administered Subcutaneously in Pituitary-suppressed Healthy Premenopausal Female Participants of Japanese or Caucasian Origin

Status: Recruiting

Phase of Trial: Phase I

Latest Information Update: 12 Dec 2025

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At a glance

Drugs Ethinylestradiol/desogestrel (Primary) ; Follitropin alfa/lutropin alfa (Primary)
Indications Female infertility
Focus Pharmacokinetics

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