GnRH antagonist

Cetrorelix

US: FDA-approvedEU: AuthorisedUK: AuthorisedCA: AuthorisedAU: RegisteredCH: AuthorisedBR: RegistadoRS: AuthorisedSG: RegisteredTR: Ruhsatli

Answer

Cetrorelix is authorised or registered in the US, the EU, the UK, Canada, Australia, Switzerland, Brazil, Serbia, Singapore and Turkey: 10 of the 10 registers read. No trial states a phase. It has 140 registered trials, 14 of them running. Brand names on the FDA label register: Cetrorelix Acetate and Cetrotide.

RegulatorTrial register10 regulators' registers, read 2026-09-03 to 2026-10-03 · ClinicalTrials.gov, read 2026-10-03

Not medical, legal or regulatory advice.

Registered trials140Trial register ClinicalTrials.gov
Running now14Trial register recruiting, active or enrolling
Results posted8Trial register with results on the register
Stopped early7.1%Trial register all peptides: 10%

140 trials by status

Trial register
Running 14Completed 74Stopped early 10Status unknown 42

ClinicalTrials.gov · read 2026-10-03 · 8 trials have posted results

Trials first submitted per year

Trial register

ClinicalTrials.gov first-submitted date, last 10 years · read 2026-10-03. 2026 is not complete. 65 trials carry no first-submitted date (EU CTIS publishes none, or the year is outside this range).

Status by jurisdiction

World map
Authorised or registeredNot on the register, or withdrawnNot read yet, or status unknown
WhereStatusRegisterRead
United StatesFDA-approvedFDA, openfda2026-10-03
European UnionAuthorisedEMA, ema2026-10-03
United KingdomAuthorisedMHRA, uk-mhra2026-10-03
CanadaAuthorisedHealth Canada, ca-dpd2026-10-03
AustraliaRegisteredTGA, au-artg2026-10-03
SwitzerlandAuthorisedSwissmedic, ch-swissmedic2026-10-03
BrazilRegistadoANVISA, br-anvisa2026-10-03
SerbiaAuthorisedALIMS, rs-alims2026-09-03
SingaporeRegisteredHSA, sg-hsa2026-09-03
TurkeyRuhsatliTITCK, tr-titck2026-09-03

An EU decision applies in the 30 territories the EU register covers: its member states, and Iceland, Liechtenstein and Norway. A dashed tile has no register read for this peptide.

Side effects

Trial register
2 placebo-controlled trials · 661 people on Cetrorelix · grey is placebo
Nasopharyngitis8.9% 8.7%
Injection site pain8.5% 3.7%
Headache7.3% 7.3%
Upper respiratory infection6.9% 6%
Back pain6.2% 6.4%
ClinicalTrials.gov posted results · read 2026-10-03All side effects

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One email when the status of Cetrorelix changes on the register. You confirm your address first.

REGISTERED TRIALS

Newest 10 of 140 trials

All 140 trials
NCT07732348
Oral GnRH Antagonist (Linzagolix) Versus Injectable GnRH Antagonist in Controlled Ovarian Stimulation for In Vitro Fertilization:
not yet recruiting participants · register updated 2026-09-30
NCT07836400
Half-dose vs Conventional-dose Cetrorelix in ICSI Cycles
not yet recruiting participants · register updated 2026-09-23
NCT07340827
A Study to Compare the Efficacy and Safety of Follitropin Alfa/Lutropin Alfa Versus hMG in Japanese Participants With LH and FSH D
currently recruiting participants · register updated 2026-09-08
NCT07736261
Drospirenone-Primed Ovarian Stimulation Versus GnRH Antagonist Protocol in Poor Ovarian Responders Undergoing Freeze-All IVF/ICSI
not yet recruiting participants · register updated 2026-07-30
NCT06572930
Serum FSH Monitoring for Identification of an Optimal Range During Ovarian Stimulation
currently recruiting participants · register updated 2026-06-25
NCT06212102
Dydrogesterone Versus GnRH Antagonist in Poor Responders Undergoing Double Ovarian Stimulation
currently recruiting participants · register updated 2026-05-04
NCT05951400
Progesterone Primed Protocol Versus GnRH Antagonist in With PCO Undergoing ICSI
completed · register updated 2026-04-15
NCT02892942
NATural Ovarian Stimulation
completed · register updated 2026-04-03
NCT02890082
Preservation of Fertility by Ovarian Stimulation Associated With Tamoxifen, Prior Chemotherapy for Breast Cancer
running, but no longer enrolling · register updated 2026-03-31
NCT04719000
PErsonalized Addition of Recombinant LH in Ovarian Stimulation
currently recruiting participants · register updated 2026-03-30

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