Cetrorelix
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Routes of administration | Subcutaneous injection |
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Pharmacokinetic data | |
Bioavailability | 85% |
Protein binding | 86% |
Elimination half-life | 62.8 hours / 3mg single dose |
Excretion | Liver |
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E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
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Molar mass | 1431.06 g/mol |
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Ongoing Trials on Cetrorelix at Clinical Trials.gov Clinical Trials on Cetrorelix at Google
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US National Guidelines Clearinghouse on Cetrorelix
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Patient Resources / Community |
Patient resources on Cetrorelix Discussion groups on Cetrorelix Patient Handouts on Cetrorelix Directions to Hospitals Treating Cetrorelix Risk calculators and risk factors for Cetrorelix
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Causes & Risk Factors for Cetrorelix |
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Cetrorelix acetate is an injectable gonadotropin-releasing hormone antagonist (GnRH antagonist). A synthetic decapeptide, it is used to treat hormone-sensitive cancers of the prostate and breast (in pre-/perimenopausal women) and some benign gynaecological disorders (endometriosis, uterine fibroids and endometrial thinning). In addition, cetrorelix is used in assisted reproduction. The drug works by blocking the action of GnRH upon the pituitary, thus rapidly suppressing the production and action of LH and FSH. It is administered as a daily or weekly subcutaneous injection.
Cetrorelix is marketed by Solvay Pharmaceuticals as Cetrotide.[1]
References
Template:SIB Template:Sex hormones Template:Pituitary and hypothalamic hormones and analogues
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- GnRH antagonists
- Fertility medicine
- Endocrinology