Last reviewed · How we verify

Placebo-Repaglinide

Steno Diabetes Center Copenhagen · FDA-approved active Small molecule

Repaglinide is a meglitinide that stimulates insulin secretion from pancreatic beta cells by closing ATP-sensitive potassium channels.

Repaglinide is a meglitinide that stimulates insulin secretion from pancreatic beta cells by closing ATP-sensitive potassium channels. Used for Type 2 diabetes mellitus.

At a glance

Generic namePlacebo-Repaglinide
SponsorSteno Diabetes Center Copenhagen
Drug classMeglitinide (rapid-acting insulin secretagogue)
TargetATP-sensitive potassium channel / Sulfonylurea receptor
ModalitySmall molecule
Therapeutic areaDiabetes
PhaseFDA-approved

Mechanism of action

Repaglinide binds to sulfonylurea receptors on pancreatic beta cells, leading to closure of ATP-sensitive potassium channels and subsequent depolarization. This triggers calcium influx and insulin exocytosis, thereby lowering blood glucose levels. The drug has a rapid onset and short duration of action, making it suitable for mealtime glucose control.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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