Treatment with the gonadotrophin-releasing hormone antagonist ganirelix in women undergoing ovarian stimulation with recombinant follicle stimulating hormone is effective, safe and convenient: results of a controlled, randomized, multicentre trial

• Published in: Human reproduction (Oxford) Vol. 15; no. 7; pp. 1490 - 1498
• Main Authors: Borm, G., Mannaerts, B.
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01.07.2000
• Subjects: Biological and medical sciences; buserelin; ganirelix; Genital system. Reproduction; GnRH agonist; GnRH antagonist; ICSI; IVF; Medical sciences; ovarian stimulation; Pharmacology. Drug treatments; recombinant FSH; buserelin; ICSI; recombinant FSH; GnRH agonist; ovarian stimulation; IVF; ganirelix; GnRH antagonist; Human; Agonist; Toxicity; Multicenter study; Assisted procreation; Gonadotropin RH; Stimulation; Gonadotropin; Ganirelix; Hypothalamic hormone; In vitro fertilization embryo transfer; Ovary; Randomization; Buserelin; Adenohypophyseal hormone; Female genital system; Clinical trial; Female; Antagonist; Recombinant protein; Hormone releasing factor; Follicle stimulating hormone
• ISSN: 0268-1161; 1460-2350
• DOI: 10.1093/humrep/15.7.1490

A multicentre, open-label, randomized study of the gonadotrophin-releasing hormone (GnRH) antagonist ganirelix (Orgalutran®/Antagon™) was performed in women undergoing ovarian stimulation with recombinant FSH (rFSH: Puregon®). The study was designed as a non-inferiority study using a long protocol of buserelin (intranasal) and rFSH as a reference treatment. A total of 730 subjects was randomized in a treatment ratio of 2:1 (ganirelix:buserelin) using an interactive voice response system which stratified for age, type of infertility and planned fertilization procedure [IVF or intracytoplasmic sperm injection (ICSI)]. The median duration of GnRH analogue treatment was 5 days in the ganirelix group and 26 days in the buserelin group, whereas the median total rFSH dose was 1500 IU and 1800 IU respectively. In addition, in the ganirelix group the mean duration of stimulation was 1 day shorter. During ganirelix treatment the incidence of LH rises (LH ≥10 IU/l) was 2.8% versus 1.3% during rFSH stimulation in the buserelin group. On the day of triggering ovulation by human chorionic gonadotrophin (HCG), the mean number of follicles ≥11 mm diameter was 10.7 and 11.8, and the median serum oestradiol concentrations were 1190 pg/ml and 1700 pg/ml in the ganirelix and buserelin groups respectively. The mean number of oocytes per retrieval was 9.1 and 10.4 respectively, whereas the mean number of good quality embryos was 3.3 and 3.5 respectively. The fertilization rate was equal in both groups (62.1%), and the same mean number of embryos (2.2) was replaced. The mean implantation rates were 15.7% and 21.8%, and the ongoing pregnancy rates per attempt were 20.3% and 25.7% in the ganirelix and buserelin groups respectively. Evaluation of all safety data indicated that the ganirelix regimen was safe and well tolerated. The overall incidence of ovarian hyperstimulation syndrome was 2.4% in the ganirelix group and 5.9% in the reference group. The results of this study support a safe, short and convenient treatment regimen of ganirelix, resulting in a good clinical outcome for patients undergoing ovarian stimulation for IVF or ICSI.