Αναζήτηση Δραστικών

GOSERELIN

Εμπορικές Ονομασίες

  • DRUGBANK - Goserelin
  • indication:

    Breast cancer; Prostate carcinoma; Endometriosis

  • pharmacology:

  • mechanism:

    ZOLADEX is a synthetic decapeptide analogue of LHRH. ZOLADEX acts as a potent inhibitor of pituitary gonadotropin secretion when administered in the biodegradable formulation. The result is sustained suppression of LH and serum testosterone levels.

  • toxicity:

    No experience of overdosage from clinical trials

  • absorprion:

    Inactive orally, rapidly absorbed following subcutaneous administration

  • halflife:

    4-5 hours

  • roouteelimination:

    Clearance of goserelin following subcutaneous administration of a radiolabeled solution of goserelin was very rapid and occurred via a combination of hepatic and urinary excretion. More than 90% of a subcutaneous radiolabeled solution formulation dose of goserelin was excreted in urine.

  • volumedistribution:

    * 44.1 ± 13.6 L [subcutaneous administration of 250 mcg]

  • clearance:

    * 121 +/- 42.4 mL/min [prostate cancer with 10.8 mg depot]