Approved

Cetrorelix: Uses, Mechanism, and Side Effects

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

Women undergoing fertility treatment often want to know how the medications in their protocol keep a cycle on track. Cetrorelix is one of the drugs used specifically to prevent an early hormonal surge that could disrupt egg retrieval timing.

Key takeaways

  • Cetrorelix is approved to inhibit premature LH surges during controlled ovarian stimulation.
  • It is marketed as cetrorelix acetate for injection.
  • The drug does not carry a boxed warning.
  • More than 140 registered trials have studied cetrorelix, largely in IVF settings.
  • The most reported adverse event in safety data is ovarian hyperstimulation syndrome.

What Cetrorelix Is

Cetrorelix belongs to a class of injectable peptides used in assisted reproduction. Its molecular structure (PubChem CID 25074887) reflects a synthetic decapeptide designed to interact with reproductive hormone signaling during fertility cycles.

What Cetrorelix Is Approved For

Cetrorelix acetate for injection is approved for the inhibition of premature LH surges in women undergoing controlled ovarian stimulation. This use supports fertility protocols by helping control the timing of ovulation during treatment cycles. No boxed warning is associated with this label.

What the Evidence Shows

Cetrorelix has been studied in 142 registered clinical trials. One completed phase 2/3 trial examined endometrial injury and IVF outcome parameters in patients with failed IVF cycles. Other trials have compared cetrorelix-based antagonist protocols against alternative ovarian stimulation approaches, including a terminated study and one with unknown status evaluating outcomes in polycystic ovary syndrome patients undergoing IVF or ICSI.

Reported Side Effects

Reported safety data reflect counts of adverse event reports, not confirmed incidence or causation. The most frequently reported event is ovarian hyperstimulation syndrome (135 reports), a known risk in ovarian stimulation cycles. Other commonly reported events include drug ineffectiveness, premature ovulation, and spontaneous abortion, along with gastrointestinal and abdominal complaints such as ascites, abdominal distension, abdominal pain, and nausea.

FAQ

What is cetrorelix used for?
Cetrorelix is approved to prevent premature LH surges in women undergoing controlled ovarian stimulation as part of fertility treatment. It helps keep the timing of ovulation aligned with the treatment protocol.
Does cetrorelix have a boxed warning?
No, cetrorelix's label does not carry a boxed warning.
What are the most commonly reported side effects of cetrorelix?
The most frequently reported event is ovarian hyperstimulation syndrome, followed by reports of drug ineffectiveness, premature ovulation, and spontaneous abortion. Gastrointestinal complaints like abdominal distension, abdominal pain, and nausea are also reported. These are counts of adverse event reports, not confirmed rates of occurrence.
How much clinical research exists on cetrorelix?
Cetrorelix has been studied in more than 140 registered clinical trials, many focused on IVF and ovarian stimulation protocols. Sample trials include studies comparing antagonist protocols to other stimulation approaches in IVF and ICSI patients.
What brand name is cetrorelix sold under?
Cetrorelix is marketed as cetrorelix acetate for injection.
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: FDA label (DailyMed) ClinicalTrials.gov FDA FAERS PubChem

Updated 2026-09-19