Approved

Cetrorelix: Uses, Evidence, and Side Effects

Drafted by an automated content engine from FDA, PubChem, ClinicalTrials.gov, NIH DSLD, and Open Beauty Facts data.

Molecular formulaC70H92ClN17O14
Molecular weight1431 g/mol
Registered trials142
PubChem CID25074887
Brand namescetrorelix acetate

Overview

Women undergoing controlled ovarian stimulation need a way to prevent the body from ovulating too early. Cetrorelix acetate is an injectable peptide approved for exactly that purpose.

Key Takeaways

  • Cetrorelix acetate is approved to inhibit premature LH surges during controlled ovarian stimulation.
  • It is marketed under the brand name cetrorelix acetate.
  • More than 140 trials involving cetrorelix are registered, spanning fertility and other indications.
  • FAERS reports are dominated by ovarian hyperstimulation syndrome and related reproductive events.
  • Reported gastrointestinal effects include abdominal distension, abdominal pain, and nausea.

What Cetrorelix Is

Cetrorelix is a synthetic peptide compound, identifiable by PubChem CID 25074887, formulated for injection. It is sold as cetrorelix acetate.

What Cetrorelix Is Approved For

Cetrorelix acetate for injection is indicated for the inhibition of premature LH surges in women undergoing controlled ovarian stimulation. This use targets a specific step in assisted reproduction protocols, preventing early ovulation before egg retrieval.

What the Evidence Shows

More than 140 trials involving cetrorelix are registered on ClinicalTrials.gov. One phase 3 trial examined cetrorelix pamoate regimens in patients with symptomatic benign prostatic hypertrophy, though it was terminated. A phase 2 trial is currently recruiting to compare dydrogesterone with GnRH antagonist therapy, including cetrorelix, in poor responders undergoing double ovarian stimulation. A separate recruiting study is evaluating serum FSH monitoring during ovarian stimulation.

Reported Side Effects

FAERS data reflect adverse event reports, not confirmed incidence or causation. The most frequently reported reaction is ovarian hyperstimulation syndrome (133 reports), reflecting cetrorelix's role in fertility treatment. Other reproductive events include drug ineffective (42), premature ovulation (40), and spontaneous abortion (38). Gastrointestinal and abdominal complaints also appear, including ascites (28), abdominal distension (27), abdominal pain (26), and nausea (24).

FAQ

What is cetrorelix used for?
Cetrorelix acetate is approved to inhibit premature LH surges in women undergoing controlled ovarian stimulation. It is used as part of assisted reproduction protocols to help time egg retrieval correctly.
Is cetrorelix the same as cetrorelix acetate?
Cetrorelix acetate is the approved brand formulation of the peptide cetrorelix. It is administered by injection for its approved fertility-related indication.
What are the most common side effects reported with cetrorelix?
The most frequently reported reactions involve ovarian hyperstimulation syndrome, along with premature ovulation and spontaneous abortion. Gastrointestinal complaints such as abdominal distension, abdominal pain, and nausea are also reported. These figures come from adverse event reports and do not establish that cetrorelix caused the reaction.
Does cetrorelix carry a boxed warning?
No, the cetrorelix acetate label does not carry a boxed warning.
Is cetrorelix still being studied in clinical trials?
Yes, more than 140 trials involving cetrorelix are registered. Current recruiting studies include research on ovarian stimulation protocols and FSH monitoring.
This page is an editorial information resource. It does not sell, prescribe, or recommend any medication. Content is editorial information, not medical advice. Talk to your doctor before any treatment decision.

Sources: DailyMed label ClinicalTrials.gov FDA FAERS PubChem

Updated 2026-08-03