Clinical trial

Luveris® (Lutropin Alfa for Injection) in Women With Hypogonadotropic…

NCT00328926 · EMD Serono, Industry · Terminated

Key facts

NCT number NCT00328926
Title Luveris® (Lutropin Alfa for Injection) in Women With Hypogonadotropic Hypogonadism (Luteinizing Hormone [LH] Less Than [<] 1.2 International Unit Per Liter [IU/L])
Official title A Phase IV, Multicenter, Randomized, Double-blinded, Clinical Trial to Confirm the Efficacy of the 75 IU Dose of Luveris® vs. Placebo When Administered With Follitropin Alfa for Induction of Follicular Development and Pregnancy in Hypogonadotropic Hypogonadal Women With Profound LH Deficiency, as…
Lead sponsor EMD Serono, Industry
Status Terminated
Phase Phase 4
Study type Interventional
Conditions Hypogonadotropic Hypogonadism
Intervention type Drug
Interventions Luveris® 75 IU, Luveris® 25 IU, Placebo, Recombinant human follicle stimulating hormone (r-hFSH), Recombinant human chorionic gonadotropin (r-hCG)
Enrollment 11
Start date Mar 1, 2006
Primary completion May 1, 2012
Completion May 1, 2012
First posted May 24, 2006
Last update posted Aug 7, 2013
Countries United States

At a glance

  • 1–9 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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