Drug lookup
Drug reference

Ganirelix

Gonadotropin-releasing hormone (GnRH) antagonist (decapeptide) · Gonadotrophin-affecting drug for infertility and controlled ovarian stimulation

Also known as ANTAGON

START
0.25 mg SC once daily from day 5–6 of FSH stim; continue to hCG trigger
TYPICAL MAX
0.25 mg SC once daily
STOP IF
Anaphylaxis or established pregnancy
WATCH
Pregnancy confirmation; LH/oestradiol; OHSS monitoring
CDSCO approvedSchedule HATC H01CC01
Renal dose adjustmenteGFR mL/min/1.73m²
CAUTIONStandard dosing30AVOIDAvoid — limited data90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
1hONSET1.5hPEAK16h1dDURATION
ONSET
1h · SC absorption
PEAK
1.5h · Tmax
16h ·
DURATION
1d · once-daily
EXCRETION
Faecal and renal — metabolites
route + CYP
INTERACTIONS
1 major
SEVERE in our sources
PREGNANCY
Contraindicated — fetal harm if dosing continues after conception.
FDA category + note
Top interactionssee all 5
  • Gnrh AgonistsSevereDatabaseKimi deep-research + Cla

Mechanism

Synthetic decapeptide that competitively blocks pituitary GnRH receptors, suppressing LH and FSH release immediately — used to prevent premature LH surge during controlled ovarian hyperstimulation in ART.

Indications

Inhibition of premature LH surge in women undergoing controlled ovarian hyperstimulation (in-vitro fertilisation)

Dosing

Adult
0.25 mg SC once daily starting on day 5 or 6 of FSH stimulation; continue until day of hCG trigger.
Pediatric
Not applicable.
Renal adjustment
Avoid in severe impairment (limited data).
Hepatic adjustment
No adjustment.
Geriatric
Not applicable (reproductive-age use).
Max dose
0.25 mg SC once daily

Pharmacokinetics

Onset
LH suppression within hours
Peak effect
~1–2 h (SC Tmax)
Duration
~24 h (once-daily)
Half-life
~16 h
Bioavailability
~91% (SC)
Protein binding
~82%
Metabolism
Peptidase hydrolysis
Excretion
Faecal and renal (metabolites)

Contraindications

  • Pregnancy
  • Hypersensitivity to ganirelix or GnRH analogues
  • Severe renal impairment

Side effects

Common
Injection-site reactionsHeadacheNauseaPelvic / abdominal pain
Serious
  • Severe hypersensitivity (rare, anaphylaxis)
  • Ovarian hyperstimulation syndrome (background ART risk)
  • Fetal harm if used in established pregnancy

Pregnancy & lactation

Pregnancy

Contraindicated — fetal harm if dosing continues after conception.

Lactation

Avoid (limited data).

Drug interactions

Gnrh Agonists
Severe
Database

Pharmacologic antagonism

Do not co-administer in same cycle

Source: Kimi deep-research + Cla

Combined Hormonal Contraceptives
Mild
Database

Counteracts GnRH inhibition (intended pre-treatment in some protocols)

Specialist protocol

Source: Kimi deep-research + Cla

Fsh
Mild
Database

Complementary in ART (intended)

Standard ART protocol

Source: Kimi deep-research + Cla

Hcg
Mild
Database

Sequential in ART (intended)

Stop ganirelix at hCG trigger

Source: Kimi deep-research + Cla

Other Peptide Hormones
Mild
Database

No significant interaction

No action required

Source: Kimi deep-research + Cla

5 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.

Related guidelines

Ask House about Ganirelix

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e, Katzung, BNF·Verified: 2026-05-20 · House clinical team·Cockpit curated: 2026-05-20