COMPARISON

Goserelin vs Leuprolide

3 attributes held for at least one of the two. 2 differ. Each value carries the register it came from and the date that register was read.

Answer

Goserelin is authorised or registered in 9 and Leuprolide in 8 of the 10 registers read. Goserelin: highest phase Phase 4 (after approval). Leuprolide: highest phase Phase 3 (2 phase 3 trials, 0 with posted results). 179 registered trials include both.

States no view on which is preferable, safer or more effective. Not medical advice.

GoserelinLeuprolide
Registered trials
differs
449
clinicaltrials.gov · 2026-10-03
520
clinicaltrials.gov · 2026-10-03
FDA label
differs
FDA-approved: ZOLADEX
openfda · 2026-10-03T17:23:44.062Z
FDA-approved: Vabrinty
openfda · 2026-10-03T17:23:44.062Z
EU authorisation
Nothing on record
ema read 2026-08-31
Nothing on record
ema read 2026-08-31

SIDE EFFECTS

Most common side effects, each beside its own placebo

Side effectGoserelinplaceboLeuprolideplacebo
Arthralgia38.8%36.2%27.5%20.9%
Hot flush35.2%34.7%68.8%57.3%
Fatigue26.6%25.5%42.8%32.8%
Diarrhoea24.5%19.9%13.9%8.5%
Back pain22.7%21.4%17.0%15.3%
Neutropenia57.9%6.5%--
Neutrophil count decreased35.5%1.5%--
Nausea23.1%19.1%--
Anaemia21.8%11.0%--
Leukopenia19.7%3.9%--
Fall--20.4%14.1%
Hypertension--16.4%15.1%
Asthenia--11.0%5.9%
Pain in extremity--11.0%10.2%
Dizziness--11.0%10.5%

Trial register Goserelin: 2 placebo-controlled trials; Leuprolide: 2. Each peptide is compared with placebo in its own trials, not with the other: a dash means the event is not in that peptide's top list. Goserelin side effects · Leuprolide side effects

LEGAL STATUS

Approval in each country read

CountryGoserelinLeuprolideRegister
United StatesFDA-approvedFDA-approvedRegulator FDA
European UnionNot on the registerNot on the registerRegulator EMA
United KingdomAuthorisedAuthorisedRegulator MHRA
CanadaAuthorisedAuthorisedRegulator Health Canada
AustraliaRegisteredStatus unknownRegulator TGA
SwitzerlandAuthorisedAuthorisedRegulator Swissmedic
BrazilRegistadoRegistadoRegulator ANVISA
SerbiaAuthorisedAuthorisedRegulator ALIMS
SingaporeRegisteredRegisteredRegulator HSA
TurkeyRuhsatliRuhsatliRegulator TITCK

HEAD TO HEAD

179 registered trials include both

NCT05827081Phase IIIb Study of Ribociclib + ET in Early Breast Cancer
RECRUITING · updated 2026-10-02
NCT03070886Antiandrogen Therapy and Radiation Therapy With or Without Docetaxel in Treating Patients With Prostate Cancer That Has Been Removed by Surgery
ACTIVE_NOT_RECRUITING · updated 2026-09-14
NCT07801898Neoadjuvant Endocrine Therapy Combined With Chemotherapy in ER-positive, HER2-negative Stage I-III Breast Cancer
NOT_YET_RECRUITING · updated 2026-09-03
NCT04557059A Study of Adding Apalutamide to Radiotherapy and LHRH Agonist in High-Risk Patients With Hormone-Sensitive Prostate Cancer
ACTIVE_NOT_RECRUITING · updated 2026-08-28
NCT07782840QL1706 Plus Neoadjuvant Endocrine Therapy in HR-Positive/HER2-Negative Breast Cancer With a Poor Response to Neoadjuvant Chemotherapy
NOT_YET_RECRUITING · updated 2026-08-26
NCT07596212BRE-06: Study to Increase Tolerance to Aromatase Inhibitors for Patients With Early-Stage Hormone Receptor Positive Breast Cancer Who Developed Hypoactive Sexua
NOT_YET_RECRUITING · updated 2026-08-24
NCT04423211Treating Prostate Cancer That Has Come Back After Surgery With Apalutamide and Targeted Radiation Based on PET Imaging
RECRUITING · updated 2026-08-19
NCT04513717Two Studies for Patients With High Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a More Intense Treatm
ACTIVE_NOT_RECRUITING · updated 2026-08-17
NCT05050084Two Studies for Patients With Unfavorable Intermediate Risk Prostate Cancer Testing Less Intense Treatment for Patients With a Low Gene Risk Score and Testing a
ACTIVE_NOT_RECRUITING · updated 2026-08-17
NCT03332797A Study of GDC-9545 Alone or in Combination With Palbociclib and/or Luteinizing Hormone-Releasing Hormone (LHRH) Agonist in Locally Advanced or Metastatic Estro
ACTIVE_NOT_RECRUITING · updated 2026-08-13
NCT04126070Nivolumab + Docetaxel + ADT in mHSPC Patients With DDRD or Inflamed Tumors
ACTIVE_NOT_RECRUITING · updated 2026-08-12
NCT01786265Finite Androgen Ablation With or Without Abiraterone Acetate and Prednisone in Treating Patients With Recurrent Prostate Cancer
ACTIVE_NOT_RECRUITING · updated 2026-08-11
NCT07751133Evaluating Hormone Therapy to Achieve Optimal Doses in Metastatic Prostate Cancer
NOT_YET_RECRUITING · updated 2026-08-07
NCT05879926Evaluating the Addition of Adjuvant Chemotherapy to Ovarian Function Suppression Plus Endocrine Therapy in Premenopausal Patients With pN0-1, ER-Positive/HER2-N
RECRUITING · updated 2026-08-04
NCT07340619Clinical Trial Evaluating the Biological Activity of a New Drug Identified as Prifetrastat (PF-07248144), Combined With Fulvestrant for the Treatment of Patient
NOT_YET_RECRUITING · updated 2026-08-03
NCT04484818Testing the Addition of Darolutamide to Hormonal Therapy (Androgen Deprivation Therapy [ADT]) After Surgery for Men With High-Risk Prostate Cancer, The ERADICAT
ACTIVE_NOT_RECRUITING · updated 2026-07-28
NCT07730151Efficacy and Safety of Darolutamide Combined With Docetaxel and ADT as Neoadjuvant Therapy for Locally Advanced Prostate Cancer.
NOT_YET_RECRUITING · updated 2026-07-28
NCT06378866Stereotactic Body Radiation Therapy Plus Immediate or Delayed Androgen Receptor Pathway Inhibitor and Androgen Deprivation Therapy or Salvage Radiation Therapy
RECRUITING · updated 2026-07-20
NCT07706933Tolerability of Dalpiciclib vs. Abemaciclib/Ribociclib in Early HR+/HER2- Breast Cancer
NOT_YET_RECRUITING · updated 2026-07-16
NCT05498272Study of Neoadjuvant PARP Inhibition Followed by Radical Prostatectomy in Patients With Unfavorable Intermediate-Risk or High-Risk Prostate Cancer With Select H
ACTIVE_NOT_RECRUITING · updated 2026-07-10

The 20 most recently updated are listed.

Values reproduce public registers on the dates shown. This comparison states no view on which compound is preferable, safer or more effective. Not medical, legal or regulatory advice.

WEEKLY

Register Watch, weekly

New trials, approvals and enforcement actions. One email a week.