Assisted reproduction

Active Ingredient: Goserelin

Indication for Goserelin

Population group: women, only adults (18 - 65 years old)

Pituitary downregulation in preparation for superovulation.

For this indication, competent medicine agencies globally authorize below treatments:

3.6 mg once

Route of admnistration

Subcutaneous

Defined daily dose

3.6 - 3.6 mg

Dosage regimen

From 3.6 To 3.6 mg once every 28 day(s)

Detailed description

Goserelin 3.6 mg is administered to downregulate the pituitary gland, as defined by serum estradiol levels similar to those observed in the early follicular phase (approximately 150 pmol/l). This will usually take between 7 and 21 days.

When downregulation is achieved, superovulation (controlled ovarian stimulation) with gonadotrophin is commenced. The downregulation achieved with a depot agonist is more consistent suggesting that, in some cases, there may be an increased requirement for gonadotrophin. At the appropriate stage of follicular development, gonadotrophin is stopped and human chorionic gonadotrophin (hCG) is administered to induce ovulation. Treatment monitoring, oocyte retrieval and fertilisation techniques are performed according to the normal practice of the individual clinic.

Active ingredient

Goserelin

Goserelin is a synthetic analogue of naturally occurring LHRH. On chronic administration goserelin results in inhibition of pituitary LH secretion leading to a fall in serum testosterone concentrations in males and serum estradiol concentrations in females.

Read more about Goserelin

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