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Elinzanetant

LYNKUET

Pronunciation: e-lin-ZA-ne-tant (lin-kyoo-ET)

Elinzanetant ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Elinzanetant ballicule

What it isDual NK1 and NK3 receptor antagonist; menopausal vasomotor symptoms.

Why this oneBlocking both neurokinin pathways targets hot flashes and associated sleep disruption without hormones.

What limits itCheck liver tests; transaminase elevation can end treatment, while somnolence and dizziness make driving unsafe.

Elinzanetant molecular structure (skeletal formula)
Molecular structure: Elinzanetant

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
Moderate to severe vasomotor symptoms due to menopauseAdults120 mg QHS120 mg QHS120 mg QHS

Renal End-stage renal disease (with or without hemodialysis): not recommended

Hepatic Moderate to severe hepatic impairment: not recommended; do not start if ALT/AST ≥2×ULN or total bilirubin ≥2×ULN

Instructions

Available strengths

Contraindications

Cautions

Adverse reactions

Pregnancy Contraindicated; may cause pregnancy loss or stillbirth.

Lactation No human data; elinzanetant present in animal milk.

Cost

Elinzanetant (LYNKUET)
What pharmacies pay · NADAC 9/30/26
Strength#/mogeneric $/mobrand $/moCostPlus
60 mgcap30 qd—$299.12not offered

Generic entry2039 est.

NO BOXED WARNINGS

Principal riskTransaminase rise

Classes and tags

Clinical profile

Therapeutic safety burden1 / 4
Overdose danger1 / 4
Weight-gain liability0 / 4
Sedation liability1 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk4 / 4

Legacy pregnancy categoryNot assigned — PLLR-era drug

Defining liabilityGenerally tolerated at therapeutic doses; clinically important risks are agent-specific and increase with interactions or organ impairment.

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