Konten bukti dipertahankan dalam bahasa Inggris.

Penggambaran struktur ideal untuk Gonadorelin

Konformer ideal yang dibangun dari urutan; bukan struktur eksperimental atau prediksi.

Sekilas

ENTRY TYPE
approved drug
IDENTITY
Sequence verified

No structure asset recorded

TOP EVIDENCE
Grade A — Induction of ovulation, primary hypothalamic amenorrhea
MAJOR STATUS
Jurisdiction-specific — see status table
SPORT
Prohibited — as of 2026-08-06
VERIFIED
2026-08-06

Bottom line

Gonadorelin is synthetic gonadotropin-releasing hormone (GnRH), a decapeptide identical in sequence to the human hypothalamic hormone. It is approved for induction of ovulation in women with primary hypothalamic amenorrhea when administered in a pulsatile fashion (Lutrepulse, Canada/US limited availability), and as a veterinary reproductive agent in cattle (Factrel). The short (~4 min) necessitates pump-based pulsatile delivery for fertility use. Gonadorelin is distinct from, and should not be confused with, GnRH agonist analogues (leuprolide, goserelin, triptorelin, nafarelin) that are modified for prolonged action and chemical castration.

Identity and composition

FieldVerified information
Preferred nameGonadorelin
Key aliasesGnRH, LHRH, gonadotropin-releasing hormone; Lutrepulse (human), Factrel (veterinary)
Molecular/sequence identitypGlu-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly-NH2 (decapeptide)
Modifications/formC-terminal amide; N-terminal pyroglutamyl; identical to human GnRH
Stable identifiers 638793 (gonadorelin HCl); UNII Q2E1H3G52I
Identity caveatsOften confused with GnRH agonist analogues; distinct from leuprolide, goserelin, triptorelin, nafarelin, which contain D-amino acid substitutions and have longer half-lives

Development and approval status

JurisdictionStatus and indicationProduct/sourceAs of
Canada (Health Canada)Approved; induction of ovulation in primary hypothalamic amenorrheaLutrepulse (Ferring) — commercially discontinued2016 monograph
US (FDA)Human: Lutrepulse was FDA-approved but commercially discontinued (not formally withdrawn). Veterinary: Factrel for cattle only (Zoetis)Factrel (Zoetis) NADA 139-237Lutrepulse commercially discontinued; Vet: 2014
EU (EMA)Not actively marketed as human drug; historical GnRH diagnostic useVarious (diagnostic)Not current
Status is multi-axis
Gonadorelin authorization and sport-status profileFour medicine-authorization axes reproduce only documented status rows; sport status is shown separately.UNITED STATESHuman: Lutrepulse wasFDA-approved but commerciallySOURCE / AS OFROW 2 / Lutrepulse commercially discontinued; Vet: 2014EU/EEANot actively marketed as humandrug; historical GnRHSOURCE / AS OFROW 3 / Not currentUNITED KINGDOMSOURCE ROW OMITTEDSEE AUDIT REASONSOURCE / AS OFNOT PRESENT / NOT RECORDEDOTHER DOCUMENTEDApproved; induction ofovulation in primarySOURCE / AS OFROW 1 / 2016 monographSPORT STATUS — SEPARATE FROM MEDICINE AUTHORIZATIONWADA: GnRH (gonadorelin) is explicitly prohibited at all times in males under S2.2.1; theList does not make that prohibition conditional on a demonstrated androgen effect. In female
Authorization belongs to the named product, use, place, and date; sport status is independent.
Alternatif teks
UNITED STATES
US (FDA): Human: Lutrepulse was FDA-approved but commercially discontinued (not formally withdrawn). Veterinary: Factrel for cattle only (Zoetis)
EU/EEA
EU (EMA): Not actively marketed as human drug; historical GnRH diagnostic use
UNITED KINGDOM
No UNITED KINGDOM row is present in the source status table
OTHER DOCUMENTED
Canada (Health Canada): Approved; induction of ovulation in primary hypothalamic amenorrhea

Sport status: WADA: GnRH (gonadorelin) is explicitly prohibited at all times in males under S2.2.1; the List does not make that prohibition conditional on a demonstrated androgen effect. In female athletes under 18, GnRH analogues are included in the 2026 Monitoring Program, which is not prohibition.

Mechanism and pharmacology

agonist at the GnRH receptor on anterior pituitary gonadotrophs, triggering LH and FSH synthesis and secretion. Pulsatile administration mimics the natural hypothalamic secretory pattern, restoring gonadal function. Continuous administration causes receptor desensitisation (the basis of GnRH agonist therapy for prostate cancer). ~4 min; rapidly cleared.

Evidence by claim

Claim/indicationStageGradeBest human evidenceMain resultImportant limitations
Induction of ovulation, primary hypothalamic amenorrheaApproved (Canada)AControlled studies (Lutrepulse monograph)68% ovulation rate with 5 µg i.v. q90 minRequires pump; limited to specific diagnosis; product availability limited
Tingkat bukti
  • AKelas A: Mapan untuk penggunaan berlabel tertentu
  • BKelas B: Bukti manusia moderat
  • CKelas C: Bukti manusia awal
  • DKelas D: Hanya praklinis
  • EKelas E: Klaim anekdot/pemasaran
  • XKelas X: Bukti bertentangan atau tidak mendukung klaim
Pelajari lebih lanjut tentang penilaian bukti
Claim-evidence profile
Gonadorelin claim-evidence profileA: 1 claim; B: 0 claims; C: 0 claims; D: 0 claims; E: 0 claims; X: 0 claimsCONTRADICTORY / NON-SUPPORTIVEA — Established for a specific labeled useGrade A: Established for a specific labeled use — current approval plus adequate controlled trials and post-market context.1 claimInduction of ovulation, primary…B — Moderate human evidenceGrade B: Moderate human evidence — multiple controlled studies or a strong pivotal study, but no current approval for the claim.0 claimsC — Preliminary human evidenceGrade C: Preliminary human evidence — small, uncontrolled, surrogate-endpoint, or early-phase studies.0 claimsD — Preclinical onlyGrade D: Preclinical only — in vitro or animal evidence with no adequate human efficacy evidence.0 claimsE — Anecdotal/marketing claimGrade E: Anecdotal/marketing claim — testimonials, extrapolation, or vendor claims without adequate scientific support.0 claimsX — Evidence contradicts or does not support the claimGrade X: Evidence contradicts or does not support the claim — adequate negative evidence, failed program, or claim inconsistent with the studied material.0 claims
This counts the page's claim rows; it does not average them into a score.
Alternatif teks

Text alternative for the claim-evidence diagram. Each grade is defined below:

AEstablished for a specific labeled use
1 claim: Induction of ovulation, primary hypothalamic amenorrhea
BModerate human evidence
0 claims
CPreliminary human evidence
0 claims
DPreclinical only
0 claims
EAnecdotal/marketing claim
0 claims
XEvidence contradicts or does not support the claim
0 claims
United StatesHuman: Lutrepulse was FDA-approved but commercially discontinued (not formally withdrawn). Veterinary: Factrel for cattle only (Zoetis)
EU/EEANot actively marketed as human drug; historical GnRH diagnostic use
OtherApproved; induction of ovulation in primary hypothalamic amenorrhea

Key studies

StudyDesign/populationExposure studiedEndpoints and resultLimitations
Lutrepulse clinical program and controlled; women with primary hypothalamic amenorrheaPulsatile gonadorelin 1-20 µg s.c./i.v. q90 minOvulation in 68% (i.v. 5 µg regimen)Small overall database; no longer widely available

Dose and administration evidence

Approved labeled regimen

The label summary below is product-, indication-, and jurisdiction-specific; consult the full current label and a licensed clinician/pharmacist.

Studied regimens (not recommendations)

What is not established

No established or recommended human dose for any indication other than ovulation induction in primary hypothalamic amenorrhea.

Safety

Established label risks

  • Anaphylaxis reported with gonadorelin HCl (Factrel) — bronchospasm, tachycardia, flushing, urticaria.

  • Antibody formation in ~3% with s.c. administration (Factrel); may reduce efficacy.

  • Injection site reactions.

  • Ovarian hyperstimulation (rare with pulsatile vs. gonadotropins).

Human-study signals

  • Minimal systemic adverse effects at recommended doses.

Unknowns and product-quality risks

  • No long-term safety data beyond fertility treatment cycles.

  • No adequate studies in men.

  • Online "gonadorelin" products are not equivalent to pharmaceutical-grade Lutrepulse.

Interactions and special populations

  • Pregnancy: Used only as part of fertility treatment.

  • Ovarian hyperstimulation: Monitor; less common than with hMG.

  • Hepatic/renal: Not formally studied; no dose adjustment known.

Regulatory, compounding, and sport notes

  • US/Canada: Prescription only; Lutrepulse limited availability.

  • : GnRH (gonadorelin) is explicitly prohibited at all times in males under S2.2.1; the List does not make that prohibition conditional on a demonstrated androgen effect. In female athletes under 18, GnRH analogues are included in the 2026 Monitoring Program, which is not prohibition.

  • Veterinary: Factrel approved for cattle only.

  • Compounding: Compounded GnRH exists but not FDA-reviewed; not interchangeable with approved product.

Evidence gaps

Search notes

  • Databases and registries: DailyMed, Drugs@FDA, Health Canada DPD, PubMed, EMA

  • Search terms: gonadorelin, Lutrepulse, Factrel, pulsatile GnRH, hypothalamic amenorrhea

  • Last searched: 2026-08-06

  • Inclusion emphasis: Approved labels, clinical studies

Sources

Suara para ahli

Apa kata para ahli

Komentar adalah opini, bukan bagian dari tinjauan bukti; penyertaan bukan berarti dukungan.

Tidak ditemukan komentar ahli terverifikasi untuk senyawa ini dalam sumber yang diterima atlas ini — literatur tinjauan sejawat, komunikasi universitas, rumah sakit, dan perhimpunan medis, regulator, serta jurnalisme sains bernama.

Tidak adanya komentar bukanlah bukti tentang senyawa ini baik positif maupun negatif.

Klaim vendor, klinik, dan media sosial dikecualikan oleh kebijakan dan tidak dihitung sebagai komentar.

Tidak ditemukan video ahli terverifikasi untuk senyawa ini dalam sumber atlas ini.

Tidak adanya video bukanlah bukti tentang senyawa ini baik positif maupun negatif.

Video vendor dan media sosial dikecualikan oleh kebijakan dan tidak dihitung.

Pertanyaan

Is gonadorelin FDA-approved?

The monograph documents Lutrepulse as historically FDA-approved for induction of ovulation in primary hypothalamic amenorrhea and commercially discontinued in the US, though not formally withdrawn. It cites a 2016 Canadian product monograph that listed the same indication and records the product as commercially discontinued. Factrel is a US-approved veterinary product for cattle only.

Is gonadorelin the same as leuprolide or goserelin?

No. Gonadorelin is synthetic GnRH with a sequence identical to endogenous human GnRH. Leuprolide, goserelin, triptorelin, and nafarelin are GnRH agonist analogues with D-amino acid substitutions and longer half-lives. They are distinct from gonadorelin and should not be confused with it.

What evidence supports gonadorelin for ovulation induction?

The 2016 Lutrepulse monograph reports a 68% ovulation rate in women with primary hypothalamic amenorrhea. The atlas grades this evidence A, but the overall database is small and the product is commercially discontinued. Its historical label summary is product-, indication-, and jurisdiction-specific.

What are gonadorelin's main safety signals?

The veterinary Factrel label reports anaphylaxis with gonadorelin HCl, including bronchospasm and tachycardia, and antibody formation in about 3%. The monograph separately lists local-site reactions and rare ovarian hyperstimulation with pulsatile human use. Online gonadorelin products are not equivalent to pharmaceutical-grade Lutrepulse.

Is gonadorelin prohibited in sport?

Yes. GnRH (gonadorelin) is explicitly prohibited at all times in males under WADA S2.2.1. In female athletes under 18, GnRH analogues are included in the 2026 Monitoring Program, which is not prohibition.

What evidence gaps remain for gonadorelin?

The monograph identifies no adequately powered modern randomized trial for ovulation induction and no data in men with hypogonadotropic hypogonadism. It also notes that the optimal pulse dose and frequency have not been formally re-evaluated.

Pembaruan penelitian

Bergabunglah dengan atlasnya. Dapatkan pembaruan bukti.

Terima catatan singkat ketika bukti peptida, status, atau catatan sumber berubah.