Degarelix record · updated 6h ago
Degarelix is a synthetic peptide that functions as a gonadotropin-releasing hormone (GnRH) antagonist. By competitively inhibiting GnRH receptors in the pituitary gland, degarelix reduces the secretion of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), leading to decreased testosterone production in the testes. This mechanism is particularly beneficial in the treatment of hormone-sensitive conditions such as prostate cancer, where testosterone can promote tumor growth.
How it works: GnRH receptor antagonist
Development stage
where Degarelix sits between preclinical work and regulatory approval- 1ClearedPreclinicalAnimal / in-vitro work
- 2ClearedPhase 1Safety in humans
- 3ClearedPhase 2Efficacy signal
- 4ClearedPhase 3Confirmatory trials
- 5CurrentApprovedCleared by a regulator
Stage is inferred from the highest trial phase in the indexed corpus and 89 registered trials. It describes the research record, not a recommendation.
Mass and formula from PubChem CID 16136245. No verified residue count for this compound.
What people are saying
anecdotal · not evidenceUnverified first-hand accounts from public forums. These are not studies: nobody checked what was taken, whether it was what the label said, or what else was going on. They count for nothing in the evidence grade above and are shown because a reader searching Degarelix will meet them anyway, and meeting them next to a graded evidence base is better than meeting them alone.