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Nateglinide

STARLIX

Pronunciation: na-TAY-gli-nide

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

What it isMeglitinide that closes beta-cell KATP channels; mealtime control in type 2 diabetes.

Why this oneIts rapid, brief action targets postprandial glucose more tightly than a sulfonylurea.

What limits itHypoglycemia follows a dose without a meal, and glucose lowering is weaker than with a sulfonylurea.

Nateglinide molecular structure (skeletal formula)
Molecular structure: Nateglinide

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
Type 2 diabetes mellitusAdults120 mg TID before meals (60 mg TID if near glycemic goal at initiation)120 mg TID120 mg TID

Renal No adjustment recommended (mild to severe impairment)

Hepatic No adjustment in mild impairment; use with caution in moderate-severe (not studied)

Skip the scheduled dose if a meal is skipped

Instructions

Available strengths

Cautions

Adverse reactions

Pregnancy Data insufficient; use only if potential benefit justifies risk to fetus

Lactation Not recommended while breastfeeding (hypoglycemia risk in infant)

Cost

Nateglinide (STARLIX)
What pharmacies pay · NADAC 9/30/26
Strength#/mogeneric $/moCostPlus
60 mgtab90 TID$16.15offered
120 mgtab90 TID$20offered

Generic entry2009

NO BOXED WARNINGS

Principal riskHypoglycemia; weaker than a sulfonylurea

Classes and tags

Clinical profile

Therapeutic safety burden2 / 4
Overdose danger2 / 4
Weight-gain liability1 / 4
Sedation liability0 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk0 / 4

Legacy pregnancy categoryMultiple / indication-, trimester- or formulation-dependent

Defining liabilityAgent-specific hypoglycemia, ketoacidosis, volume, renal or gastrointestinal toxicity.

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