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lutropin

Recombinant human luteinising hormone (gonadotropin) · Infertility treatment

START
75 IU SC once daily (with FSH 75–225 IU SC)
TYPICAL MAX
Per follicular response (typically 75 IU SC daily)
STOP IF
OHSS signs (abdominal distension, dyspnoea, weight gain), pregnancy
WATCH
Follicular tracking, oestradiol levels, OHSS surveillance
CDSCO approvedATC G03GA07
Renal dose adjustmenteGFR mL/min/1.73m²
FULLStandard ART dosing90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
4hONSET10hPEAK14h1dDURATION
ONSET
4h · SC absorption
PEAK
10h · Cmax
14h ·
DURATION
1d · once-daily
EXCRETION
Proteolytic / renal clearance
route + CYP
INTERACTIONS
none in our sources
PREGNANCY
Contraindicated (stop on pregnancy confirmation).
FDA category + note

Mechanism

Recombinant human LH (lutropin alfa) binds LH/CG receptors on ovarian theca cells (and Leydig cells) — supports androgen / oestradiol biosynthesis and follicular maturation; co-administered with FSH for severe LH/FSH deficiency in ART.

Indications

Stimulation of follicular development with FSH in women with severe LH/FSH deficiency

Dosing

Adult
75 IU SC once daily with 75–225 IU SC FSH (e.g., follitropin); titrate per follicular response.
Pediatric
Not applicable.
Renal adjustment
Limited data; standard ART dosing.
Hepatic adjustment
Limited data; standard ART dosing.
Geriatric
Not applicable.
Max dose
Per ART protocol — typically 75 IU SC daily

Pharmacokinetics

Onset
Ovarian effect over days
Peak effect
~10 h (SC Cmax)
Duration
Effect days; ovarian follicle-maturation over the ART cycle
Half-life
~10–18 h
Bioavailability
~56% (SC)
Protein binding
Not applicable (glycoprotein hormone)
Metabolism
Proteolytic catabolism
Excretion
Renal/proteolytic clearance

Contraindications

  • Tumours of pituitary / hypothalamus / ovary / breast
  • Vaginal bleeding of unknown aetiology
  • Ovarian cysts (unrelated to PCOS)
  • Pregnancy
  • Hypersensitivity

Side effects

Common
Injection-site reactionsHeadacheAbdominal painOvarian cysts
Serious
  • Ovarian hyperstimulation syndrome (OHSS)
  • Multiple pregnancy (if conception)
  • Severe hypersensitivity (rare)

Pregnancy & lactation

Pregnancy

Contraindicated (stop on pregnancy confirmation).

Lactation

Not applicable (ovulation induction).

Drug interactions

Anticoagulants
Mild
Database

OHSS-related thrombosis risk

Anticipate VTE prophylaxis if OHSS develops

Source: Kimi deep-research + Cla

Aromatase Inhibitors
Mild
Database

Possible alternative / combination

Specialist combination decisions

Source: Kimi deep-research + Cla

Fsh
Mild
Database

Synergistic for follicular maturation (intended)

Per protocol

Source: Kimi deep-research + Cla

Gnrh Agonists
Mild
Database

Standard ART pre-treatment / co-treatment

Per ART protocol

Source: Kimi deep-research + Cla

Hcg
Mild
Database

Sequential — triggers ovulation

Stop lutropin at hCG trigger

Source: Kimi deep-research + Cla

Related guidelines

Ask House about lutropin

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

Sources: KD Tripathi 7e·Verified: 2026-05-20 · House clinical team·Cockpit curated: 2026-05-20