This observational study will examine the safety and efficacy profile of Elonva (corifollitropin alfa) when administered in Korean women undergoing controlled ovarian stimulation (COS) in combination with a gonadotropin-releasing hormone (GnRH) antagonist for the development of multiple follicles in an assisted reproductive technology (ART) program.
Study Type
OBSERVATIONAL
Enrollment
472
100 or 150 microgram single subcutaneous injection
Number of Oocytes Retrieved
Time frame: At time of oocyte retrieval (up 3 days from human chorionic gonadotropin [hCG] injection)
Number of Participants who Experience Ovarian Hyperstimulation Syndrome (OHSS)
Time frame: During treatment and up to 30 days after cessation of treatment
Number of Participants who report an serious adverse event (SAE)
Time frame: During treatment and up to 30 days after cessation of treatment
Number of Participants who report an adverse event (AE)
Time frame: During treatment and up to 30 days after cessation of treatment
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.