Clinical trial

A Study to Compare the Safety and Efficacy of Cetrotide® 3 Milligram (mg) Versus…

NCT00298025 · EMD Serono, Industry · Completed

Key facts

NCT number NCT00298025
Title A Study to Compare the Safety and Efficacy of Cetrotide® 3 Milligram (mg) Versus Antagon™ in Women Undergoing Ovarian Stimulation
Official title A Phase IV, Multicenter, Open-label, Randomized Study to Compare the Safety and Efficacy of Cetrotide® 3 mg Versus Antagon™ in the Inhibition of a Premature LH Surge in a r-hFSH/hMG Stimulation Cycle With OCP Programming in Women Undergoing Ovarian Stimulation Prior to ART
Lead sponsor EMD Serono, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Infertile Women Undergoing Assisted Reproductive Technology (ART)
Intervention type Drug
Interventions Cetrotide®, Antagon ™, Recombinant human follicle stimulating hormone (r-hFSH), Human Menopausal Gonadotropin (hMG), Recombinant Human Choriogonadotropin (r-hCG)
Enrollment 185
Start date Sep 1, 2003
Primary completion May 1, 2004
Completion May 1, 2004
First posted Mar 1, 2006
Last update posted Mar 26, 2014

At a glance

  • No 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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