Ganirelix is a synthetic third generation gonadotropin-releasing hormone (G
nRH) antagonist that is administered via the subcutaneous route.
The drug competitively blocks GnRH receptors in the anterior pituitary glan
d, preventing endogenous GnRH from inducing luteinising hormone (LH) and fo
llicle stimulating hormone release.
Ganirelix effectively inhibited LH surges during controlled ovarian stimula
tion in a large, multicentre clinical trial in women undergoing in vitro fe
rtilisation. A vital pregnancy rate per embryo transfer of 40.3% was achiev
ed at weeks 5 to 6 after treatment with the 0.25 mg/day dosage.
Subcutaneous ganirelix has been generally well tolerated in clinical trials
. The most common adverse events were local injection site events, asthenia
, nausea, malaise, headache and fatigue.