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Fingolimod

GILENYA

Pronunciation: fin-GOL-i-mod (je-LEN-ya)

Fingolimod ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Fingolimod ballicule
Fingolimod GILENYA mascot mnemonic cartoon
Visual mnemonic: Fingolimod mascot
“Jill’s Fingerly mods”
QT prolongation

What it isSphingosine-1-phosphate receptor modulator trapping lymphocytes in nodes; relapsing multiple sclerosis.

Why this oneThe first oral disease-modifying therapy in MS, once daily.

What limits itFirst-dose bradycardia requires six hours of observation. Macular edema, lymphopenia, and severe rebound disease on stopping.

Fingolimod molecular structure (skeletal formula)
Molecular structure: Fingolimod

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
Relapsing forms of multiple sclerosisAdults0.5 mg QD0.5 mg QD0.5 mg QD
Relapsing forms of multiple sclerosisPeds ≥10y, >40 kg0.5 mg QD0.5 mg QD0.5 mg QD
Relapsing forms of multiple sclerosisPeds ≥10y, ≤40 kg0.25 mg QD0.25 mg QD0.25 mg QD

Renal Undefined

Hepatic No adjustment for mild-moderate impairment; closely monitor severe impairment

Instructions

Available strengths

Contraindications

Cautions

Adverse reactions

Pregnancy May cause fetal harm; registry data suggest increased major birth defects. Stop 2 months before conception; use effective contraception during and for 2 months after.

Lactation No human data; present in rat milk. Weigh developmental/health benefits of breastfeeding against maternal need.

Cost

Fingolimod (GILENYA)
What pharmacies pay · NADAC 9/30/26
Strength#/mogeneric $/moCostPlus
0.25 mgcap30 qdnot offered
0.5 mgcap30 qd$47.37offered

Generic entry2019

NO BOXED WARNINGS

Principal riskFirst-dose bradycardia; severe rebound on stopping

Classes and tags

Clinical profile

Therapeutic safety burden3 / 4
Overdose danger2 / 4
Weight-gain liability0 / 4
Sedation liability0 / 4
QT / Torsades2 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk2 / 4

Legacy pregnancy categoryNot assigned — PLLR-era drug

Defining liabilitySerious infection, cytopenias, hepatic injury and malignancy risk require laboratory and clinical monitoring.

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