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GnRH analogue (decapeptide) Pregnancy: Can cause fetal harm; expected hormonal changes increase the risk of pregnancy loss. Advise pregnant patients and females of reproductive potential of the risk to the fetus.

Triptorelin

Brand names: Decapeptyl SR, Gonapeptyl

Triptorelin is a gonadotrophin-releasing hormone (GnRH) agonist given as a depot injection, used in hormone-sensitive prostate cancer, endometriosis, uterine fibroids, central precocious puberty, and as part of assisted reproduction. It produces a reversible medical suppression of sex hormone production.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: 3.75 mg, 11.25 mg or 22.5 mg depot (strength-dependent schedule)
Route: Intramuscular injection (single injection into either buttock)
Frequency: 3.75 mg every 4 weeks; 11.25 mg every 12 weeks; 22.5 mg every 24 weeks
US labelling (Trelstar). Dosing schedule depends on the product strength selected; due to different release characteristics the dosage strengths are not additive and must be selected for the desired dosing schedule. Reconstitute lyophilised microgranules in sterile water only and administer within 2 minutes of reconstitution. Alternate injection sites periodically. Indicated for prostate cancer (monitor for tumour flare from transient testosterone rise in first weeks).

Dose auto-extracted from US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Known hypersensitivity to triptorelin or any other component of the product, or to other GnRH agonists or GnRH

Side effects

  • Hot flushes
  • Skeletal pain
  • Erectile dysfunction / impotence
  • Headache
  • Oedema in legs / leg pain; testicular atrophy

Interactions

  • No drug-drug interaction studies conducted; hepatic microsomal enzymes unlikely to be involved in metabolism
  • Hyperprolactinaemic drugs should not be used concomitantly (hyperprolactinaemia reduces pituitary GnRH receptors)

Clinical monograph

How it works

As a GnRH agonist it initially stimulates and then, with continuous administration, downregulates pituitary GnRH receptors, suppressing luteinising hormone and follicle-stimulating hormone release and so reducing testosterone or oestrogen production to castrate or postmenopausal levels.

Prescribing in practice

  • In men with prostate cancer the initial testosterone surge can cause a temporary tumour flare, which may worsen bone pain or cause spinal cord compression or urinary obstruction, so anti-androgen cover should be considered, especially with metastatic disease.
  • Long-term use reduces bone mineral density, so bone health should be considered with prolonged treatment.
  • It must not be used in pregnancy, and prolonged use causes hypo-oestrogenic effects in women that may need addition of add-back therapy.

Monitoring

Monitor the relevant hormonal response (testosterone or oestrogen and, in prostate cancer, PSA), bone mineral density with prolonged use, and clinical disease response.

Counselling the patient

  • This is given as a depot injection at regular intervals by a healthcare professional.
  • Men may notice a brief worsening of symptoms when starting; report new or worsening bone pain, weakness, or trouble passing urine.
  • Hot flushes and reduced libido are common; women may have menopause-like symptoms.

Evidence & guidelines

Efficacy across its hormone-dependent indications is supported by randomised trials and extensive clinical experience with GnRH agonist therapy.

Reference: NICE NG131; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.