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Penggambaran struktur ideal untuk Goserelin

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 — Advanced prostate cancer
MAJOR STATUS
Jurisdiction-specific — see status table
SPORT
Prohibited — as of 2026-08-06
VERIFIED
2026-08-06

Bottom line

Goserelin (Zoladex) is a synthetic decapeptide GnRH agonist available as implants for 1-month (3.6 mg) and 3-month (10.8 mg) dosing. Approved for multiple indications across oncology (prostate, breast) and gynaecology (endometriosis, endometrial thinning). Depot formulations are not interchangeable — each has specific indication, duration, and population restrictions. Initial testosterone surge may cause tumour flare; long-term therapy carries cardiovascular, metabolic, bone, and psychiatric risks listed in the label.

Identity and composition

FieldVerified information
Preferred nameGoserelin
Key aliasesZoladex (3.6 mg); Zoladex LA (10.8 mg)
Molecular/sequence identitypGlu-His-Trp-Ser-Tyr-D-Ser(tBu)-Leu-Arg-Pro-AzGly-NH2 (decapeptide)
Modifications/formD-Ser(tert-butyl) at position 6; C-terminal azaglycine amide; acetate salt
Stable identifiers 5311128; UNII 0F65R8P09N
Identity caveatsDo not confuse with other GnRH agonists (leuprolide, triptorelin, nafarelin). The 3.6 mg (monthly) and 10.8 mg (3-month) implants have different approved indications

Development and approval status

JurisdictionStatus and indicationProduct/sourceAs of
US (FDA)Approved: advanced prostate cancer, stage B2-C prostate cancer (with flutamide), endometriosis, endometrial thinning, advanced breast cancerZoladex (TerSera)1989 (3.6 mg); 1996 (10.8 mg); labels updated multiple times, latest 09/2025
EU (EMA)Approved for similar indicationsZoladex (AstraZeneca)Ongoing
UK (MHRA)ApprovedZoladexOngoing
Status is multi-axis
Goserelin authorization and sport-status profileFour medicine-authorization axes reproduce only documented status rows; sport status is shown separately.UNITED STATESApproved: advanced prostatecancer, stage B2-C prostateSOURCE / AS OFROW 1 / 1989 (3.6 mg); 1996 (10.8 mg); labels updated multiple times, latest 09/2025EU/EEAApproved for similarindicationsSOURCE / AS OFROW 2 / OngoingUNITED KINGDOMApprovedSOURCE / AS OFROW 3 / OngoingOTHER DOCUMENTEDSOURCE ROW OMITTEDSEE AUDIT REASONSOURCE / AS OFNOT PRESENT / NOT RECORDEDSPORT STATUS — SEPARATE FROM MEDICINE AUTHORIZATIONWADA: Goserelin is explicitly prohibited at all times in males under S2.2.1 as a GnRHagonist analogue. GnRH analogues are monitored, not prohibited on that basis, in female
Authorization belongs to the named product, use, place, and date; sport status is independent.
Alternatif teks
UNITED STATES
US (FDA): Approved: advanced prostate cancer, stage B2-C prostate cancer (with flutamide), endometriosis, endometrial thinning, advanced breast cancer
EU/EEA
EU (EMA): Approved for similar indications
UNITED KINGDOM
UK (MHRA): Approved
OTHER DOCUMENTED
No OTHER DOCUMENTED row is present in the source status table

Sport status: WADA: Goserelin is explicitly prohibited at all times in males under S2.2.1 as a GnRH agonist analogue. GnRH analogues are monitored, not prohibited on that basis, in female athletes under 18 in 2026.

Mechanism and pharmacology

GnRH agonist. Continuous receptor binding desensitises pituitary gonadotrophs, suppressing LH/FSH → testosterone/estradiol to castrate/menopausal levels within 2-4 weeks. Initial transient surge (flare) lasts ~1-2 weeks. implant provides sustained release via biodegradable polymer.

Evidence by claim

Claim/indicationStageGradeBest human evidenceMain resultImportant limitations
Advanced prostate cancerApprovedA vs orchiectomyEquivalent survival and objective responseNon-inferiority; flare risk
Stage B2-C prostate cancer (with flutamide + RT)ApprovedARCT with radiotherapy + flutamideImproved disease-free survivalSpecific to combination regimen
Endometriosis (pain relief)ApprovedAControlled studies; 6-month durationPain and endometriotic lesion reductionBone density loss; 6-month limit
Endometrial thinning (pre-ablation)ApprovedAControlled studiesImproved surgical conditionsShort-term use only
Advanced breast cancer (pre/perimenopausal)ApprovedARCTs vs oophorectomy/otherTumour response; overall survival benefit in ER+Only in pre/perimenopausal women
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
Goserelin claim-evidence profileA: 5 claims; 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.5 claimsAdvanced prostate cancerStage B2-C prostate cancer (with flutamide…+3 moreB — 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. All claims: Advanced prostate cancer; Stage B2-C prostate cancer (with flutamide + RT); Endometriosis (pain relief); Endometrial thinning (pre-ablation); Advanced breast cancer (pre/perimenopausal).
Alternatif teks

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

AEstablished for a specific labeled use
5 claims: Advanced prostate cancer; Stage B2-C prostate cancer (with flutamide + RT); Endometriosis (pain relief); Endometrial thinning (pre-ablation); Advanced breast cancer (pre/perimenopausal)
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 StatesApproved: advanced prostate cancer, stage B2-C prostate cancer (with flutamide), endometriosis, endometrial thinning, advanced breast cancer
EU/EEAApproved for similar indications
United KingdomApproved

Key studies

StudyDesign/populationExposure studiedEndpoints and resultLimitations
Prostate cancer comparative trial; advanced PCa (n=284)Zoladex 3.6 mg q28d vs orchiectomyEquivalent survival and testosterone suppression; small n
Endometriosis RCT-controlled; womenZoladex 3.6 mg SC q28d × 6 monthsPain reduction; laparoscopy-confirmed lesion reduction6-month limit; BMD loss

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.

  • Prostate cancer (advanced): Zoladex 3.6 mg q28d OR 10.8 mg SC q12w

  • Stage B2-C prostate (with flutamide + RT): One 3.6 mg depot → 28 days later one 10.8 mg depot; continue during RT

  • Endometriosis: Zoladex 3.6 mg SC q28d × 6 months (women ≥18 y only)

  • Endometrial thinning: 1-2 depots (3.6 mg), 4 weeks apart

  • Advanced breast cancer: Zoladex 3.6 mg SC q28d long-term

  • Route: Subcutaneous injection into anterior abdominal wall by HCP

What is not established

No established or recommended dose for any unapproved indication.

Safety

Established label risks

  • Tumour flare (initial weeks).

  • Hot flushes (>80%).

  • Sexual dysfunction, decreased erections.

  • Loss of BMD — endometriosis patients limited to 6 months.

  • Hyperglycemia/diabetes — monitor blood glucose.

  • Cardiovascular: MI, sudden cardiac death, stroke risk.

  • Hypercalcemia in bone metastases.

  • Severe cutaneous adverse reactions (SCARs, including SJS/TEN) — label updated 09/2025 (Zoladex 3.6 mg).

  • QT prolongation — androgen deprivation effect.

  • Depression (women).

  • Cervical resistance — caution with dilation for ablation.

  • Injection site injury / vascular injury reported.

Unknowns and product-quality risks

  • Long-term safety beyond 6 months for benign gynaecological use.

Interactions and special populations

  • No dose adjustment for renal/hepatic impairment (label).

  • Pregnancy: Contraindicated in benign gynae use; may cause fetal harm.

  • Lactation: Discontinue drug or nursing.

Regulatory, compounding, and sport notes

  • US FDA: Prescription only.

  • : Goserelin is explicitly prohibited at all times in males under S2.2.1 as a GnRH agonist analogue. GnRH analogues are monitored, not prohibited on that basis, in female athletes under 18 in 2026.

  • Compounding: Compounded goserelin not interchangeable with Zoladex implant.

  • Not interchangeable with other GnRH agonists at different dose schedules.

Evidence gaps

  • Direct comparisons between Zoladex and other GnRH agonists in breast cancer.

  • Optimal sequencing with newer hormonal agents in prostate cancer.

  • Long-term bone health monitoring strategies.

Search notes

Sources

  1. Zoladex (goserelin implant) 3.6 mg Prescribing Information (TerSera, revised 09/2025). https://documents.tersera.com/zoladex-us/3.6mg_MagnumPI.pdf

  2. Zoladex (goserelin implant) 10.8 mg Prescribing Information. https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/020578s51,020515s11,019726s74lbl.pdf

  3. DailyMed – ZOLADEX. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a906a5bd-d2ec-4e35-8962-c0c86c637630

  4. Medscape. Goserelin (Zoladex). https://reference.medscape.com/drug/zoladex-la-goserelin-342129

  5. PubChem CID 47725 (goserelin).

Suara para ahli

Apa kata para ahli

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Pertanyaan

Is goserelin FDA-approved?

Yes. Goserelin (Zoladex) is FDA-approved for advanced prostate cancer, stage B2-C prostate cancer (with flutamide), endometriosis, endometrial thinning, and advanced breast cancer in pre/perimenopausal women.

Is goserelin the same as leuprolide?

No. The goserelin monograph identifies leuprolide as a different GnRH agonist and cautions against confusing the products. Goserelin implants have product-specific indications and schedules, so interchangeability with other GnRH agonists should not be assumed.

What evidence supports goserelin for prostate cancer?

RCTs comparing Zoladex to orchiectomy showed equivalent survival and objective response in advanced prostate cancer. For stage B2-C disease, a combination regimen with radiotherapy and flutamide improved disease-free survival. Evidence is Grade A with a limitation of tumour flare risk.

What are goserelin's main safety signals?

Hot flushes occur in over 80% of patients. Other risks include bone mineral density loss, hyperglycemia/diabetes, cardiovascular events (MI, stroke, sudden cardiac death), QT prolongation, depression, and severe cutaneous adverse reactions including SJS/TEN (label updated 09/2025).

Is goserelin prohibited in sport?

Yes. Goserelin is explicitly prohibited at all times in males under WADA S2.2.1 as a GnRH agonist analogue. GnRH analogues are monitored (not prohibited) in female athletes under 18 in 2026.

Are the monthly and three-month goserelin implants interchangeable?

No. The monthly and three-month implants have different approved indications, durations, and population restrictions. They are not interchangeable. Compounded goserelin is also not interchangeable with Zoladex implants.

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