Recombinant gonadotrophins, in particular recombinant follitropin (fol
licle-stimulating hormone: FSH), are now available for ovarian hyperst
imulation for assisted reproduction. In contrast with urinary FSH (uro
follitropin), follitropin is available in virtually unlimited quantiti
es. Follitropin is as potent as urofollitropin in all protocols of ova
rian stimulation. Furthermore, it shows an improved purity without con
tamination by urinary proteins not related to FSH, and can be injected
subcutaneously by the patients themselves. In patients with complete
luteinising hormone (LH) deficiency, follitropin stimulates follicular
development, although serum levels of estradiol remain low. For this
group of patients the addition of LH is necessary. Ongoing phase III s
tudies on the use of recombinant LH in this indication will provide an
answer to how much LH is needed in order to guarantee sufficient foll
icular growth and hormonal response. Gonadorelin (gonadotrophin releas
ing hormone; GnRH) analogues are used to avoid the surge of endogenous
LH in ovarian stimulation protocols. Gonadorelin antagonists are now
in clinical testing for the same indication. Gonadorelin antagonists a
llow sufficient suppression of endogenous LH levels. In contrast with
gonadorelin analogues, they avoid any flare-up effect, i.e. an initial
release of gonadotrophins from pituitary reservoirs. Recombinant gona
dotrophins and gonadorelin antagonists are new tools towards a more in
dividual approach to ovarian stimulation.