Gonadorelin
A short-acting fertility hormone used in tests and specialist pump therapy.
Also called: GnRH, LHRH, gonadorelin acetate, gonadorelin hydrochloride, Factrel, Lutrepulse.
Reproductive axis peptides · Gonadotropin-releasing hormone receptor agonist · Evidence: Approved drug.
What Gonadorelin does
Gonadorelin copies a brain signal for ovulation and sperm production; fertility studies mainly use frequent pump pulses. Twice-weekly shots alongside testosterone therapy lack comparable fertility evidence. Pituitary tumors, allergy and poorly monitored hormone stimulation are key concerns.
- In studies, timed pulses from a pump helped women whose periods stopped from low brain signals to ovulate. (Studied in a trial)
- In men with diagnosed hormone deficiency, pump treatment can restore sperm production, studies show. (Studied in a trial)
- A pump form (Lutrepulse) was once approved to help women with this hormone deficiency ovulate; it is now discontinued. (Drug label)
- People report adding shots during testosterone therapy to limit testicle shrinkage; fertility benefit is unproven. (Reported by users)
Uses in the sources
- Pituitary LH-response testing is described in authorized UK and French product information. (Clinician-published) (source)
- Pulsatile pumps have been studied for ovulation and sperm production in GnRH deficiency. (Studied in a trial) (source)
- People add intermittent shots to TRT to limit testicular shrinkage; fertility benefit remains unproven. (Reported by users) (source)
- A seven-man Down syndrome pilot explored cognition; this does not establish general nootropic use. (Studied in a trial) (source)
Gonadorelin dosage
Typical reported dose: 200 mcg every 3.5 days (twice a week)
- Pituitary response test: SC: 100 mcg once single diagnostic injection, under the skin. Clinician-published. Studied in: Adults undergoing an organized pituitary test. (source)
- Pituitary response test: IV: 100 mcg once single diagnostic injection, into a vein. Clinician-published. Studied in: Adults undergoing an organized pituitary test. (source)
- LutrePulse: 10 mcg pulses: 10 mcg per pulse every 90 minutes every 90 minutes by pump, under the skin. Studied in a trial. Studied in: Women with primary amenorrhea and hypogonadotropic hypogonadism. (source)
- LutrePulse: 15 mcg pulses: 15 mcg per pulse every 90 minutes every 90 minutes by pump, under the skin. Studied in a trial. Studied in: Women with primary amenorrhea and hypogonadotropic hypogonadism. (source)
- LutrePulse: 20 mcg pulses: 20 mcg per pulse every 90 minutes every 90 minutes by pump, under the skin. Studied in a trial. Studied in: Women with primary amenorrhea and hypogonadotropic hypogonadism. (source)
- Male CHH: response-guided pump: Start 10 mcg per pulse every 90 minutes every 90 minutes by pump, under the skin. Clinician-published. Studied in: Men with confirmed congenital hypogonadotropic hypogonadism. (source)
These are doses reported in labels, trials or user reports, not a personal plan. Check the source behind each one.
How to mix Gonadorelin
Comes as: UK diagnostic 100 mcg powder vial.
Mixed with: 1.0 mL sterile water for injections for the UK 100 mcg vial..
Common vial sizes: 0.1 mg. Common water amounts: 1 mL.
- Authorized UK product instructions, not an FDA/EMA label protocol.
- These instructions do not establish stability of community 2 mg multi-dose vials.
Before mixing: UK diagnostic product: store below 25°C.
After mixing: Refrigerate after mixing and use within 24 hours; discard unused solution.
Gonadorelin side effects and risks
Reported side effects
- Pump-site skin allergy: 7/20 (35%) in one male pump cohort; not a bolus test rate., moderate (source)
- Pain, swelling or itching: UK bolus label: 0.1% to <1%., mild (source)
- Headache, dizziness or nausea: UK bolus label: 0.01% to <0.1%., mild (source)
- Allergy or airway spasm: UK label classifies hypersensitivity and bronchospasm as rare., serious (source)
- IV-line infection or vein inflammation: Historical IV line complications averaged 7%; includes more than infection., serious (source)
- Multiple pregnancy or ovarian over-response: 12% multiple pregnancy in the 1990 program; 1.6% twins in the 2022 cohort., serious (source)
- Pituitary bleeding in a tumor: unknown, serious. Sudden severe headache or vision loss needs emergency assessment. (source)
Stop and get help if
- Sudden severe headache, vision change, vomiting or collapse: Seek emergency care for possible pituitary bleeding.
- Throat swelling, wheeze or faintness after injection: Seek emergency care for possible severe allergy.
- Fever, spreading redness or chills with a pump or IV line: Get urgent assessment for possible infection.
- Severe pelvic pain, rapid weight gain or breathlessness: Get urgent assessment for ovarian over-response.
Who should avoid it
- pregnant: UK product information says not to administer during pregnancy.
- breastfeeding: UK product information says not to administer while nursing.
- tryingToConceive: Specialist fertility use requires diagnosis and monitoring.
- under18: Pediatric research is not an adult self-use regimen.
- hormoneSensitiveCancer: Precaution: gonadorelin raises sex hormones; breast or prostate cancer requires an oncology plan.
- other: GnRH can trigger bleeding into a pituitary adenoma.
- other: Prior allergy to gonadorelin or its excipients can recur.
- other: Primary gonadal failure or poor pituitary reserve can limit response; diagnose the cause first.
- testedAthlete: Prohibited at all times in male athletes under WADA S2.2.1.
- other: Stop for signs of severe allergy or a serious pump-site infection.
Interactions
- Testosterone and other sex hormones: These can alter LH/FSH response. Intermittent gonadorelin has not been shown to preserve fertility during TRT.
- Glucocorticoids: Can affect pituitary gonadotropin secretion and diagnostic interpretation.
- Prolactin-raising drugs: Dopamine antagonists can blunt the GnRH response through higher prolactin.
- Spironolactone, methyldopa and digoxin: Can alter measured gonadotropins and test interpretation.
- Other GnRH medicines: Other drugs acting on the same axis can suppress or change response; they are not dose substitutes.
- Clomiphene with ovulation induction: A historical hyperstimulation case also used clomiphene; combination monitoring matters.
Product quality risks
- An FDA recall included compounded gonadorelin because of sterility concerns.
- A June 2026 FDA warning identified an unapproved gonadorelin product. A research label does not establish approval.
- No representative assay survey of online gonadorelin vials was found.
What to expect
At least 51 studies in separate reviews, 35 in women and 16 in men. More reports are listed; twice-weekly shots alongside testosterone therapy lack a controlled fertility trial.
Key studies
- Hypothalamic amenorrhea: 35 studies: Pulsatile GnRH can induce ovulation in hypothalamic amenorrhea. (source)
- Male fertility: 16 GnRH studies: Pulsatile GnRH can restore sperm production in diagnosed hormone deficiency. (source)
- GnRH versus gonadotropins: Earlier sperm appearance did not establish a higher pregnancy rate. (source)
- Lutrepulse: multicenter fertility study: The historical program studied pump therapy, not occasional TRT injections. (source)
- LutrePulse: posted phase 3 results: Posted randomized results show an ovulation signal with higher pump doses. (source)
- FHA: 25-year pump cohort: Pump therapy produced high ovulation rates with few multiple pregnancies. (source)
Gonadorelin FAQ
- Is Gonadorelin FDA-approved? Yes: Factrel, human product; discontinued (historical diagnostic gonadorelin hydrochloride product.); Lutrepulse Kit; discontinued (historical gonadorelin acetate for GnRH-deficient ovulation induction.). All human products under these NDAs are discontinued. No approved TRT-add-on indication; veterinary Factrel is a different product.
- How do people take it? Under the skin, every 3.5 days. Source: reported by users, not an established dose.
- What's the difference between Gonadorelin and Kisspeptin-10? Gonadorelin: a short-acting fertility hormone used in tests and specialist pump therapy. Kisspeptin-10: a short-acting experimental peptide that triggers reproductive hormone release. Why people pair them: reported as a second reproductive-axis stimulant. No human combination trial was found.
- Can I take it with Kisspeptin-10? Reported as a second reproductive-axis stimulant. No human combination trial was found. Hormone and fertility effects of the combination are unknown. Source: reported by users. Ask a doctor before combining anything.
- Is it banned in sport? Yes. It is banned in and out of competition (WADA 2026). The S2.2.1 restriction applies to male athletes. The ingredient, formulation and athlete-specific therapeutic use exemption must be checked with the antidoping authority.
- How long does a mixed vial last? Refrigerate after mixing and use within 24 hours; discard unused solution.
Related to Gonadorelin
- Kisspeptin-10: A short-acting experimental peptide that triggers reproductive hormone release.
- hCG: A fertility hormone with limited testosterone add-on evidence and no proven weight-loss benefit.
Sources
- Compounding and the FDA: Questions and Answers, FDA · FDA · 2026
- FDA warning letter 729447: unapproved gonadorelin (2026-06-17), FDA · 2026
- The 2026 Prohibited List, World Anti-Doping Agency · WADA · 2026
- Therapeutic Goods (Poisons Standard—October 2026) Instrument 2026, Australian Government · Australian Government · 2026
- Bulk Drug Substances Nominated for Use in Compounding Under Section 503B of the Federal Food, Drug, and Cosmetic Act, FDA · FDA · 2025
- FDA CDER alert: compounded-drug recall for lack of sterility assurance (2022-04-26), FDA · 2022
- Gonadorelin 100 micrograms powder for solution for injection, Esteve Pharmaceuticals · 2022
- Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment., Boehm U et al. · Nature reviews. Endocrinology · 2015
- Base de Données Publique des Médicaments, ANSM
- Drugs@FDA: FDA-Approved Drugs, FDA
- Drugs@FDA: FDA-Approved Drugs, FDA
- FD&C Act Provisions that Apply to Human Drug Compounding, FDA · FDA
- PREGNYL- choriogonadotropin alfa kit, Organon
- Product information, Health Canada
- Successful ovulation and pregnancy with pulsatile GnRH pump therapy in a polycystic ovary syndrome (PCOS) patient: a case report., Wang S et al. · Frontiers in endocrinology · 2026
Sources checked: 2026-10-18.
Information only, not medical advice. Peptifacts does not sell anything and does not link to sellers.