Last reviewed · How we verify

Comparator: glipizide

Merck Sharp & Dohme LLC · Phase 3 active Small molecule

Glipizide stimulates insulin secretion from pancreatic beta cells by blocking ATP-sensitive potassium channels.

Glipizide stimulates insulin secretion from pancreatic beta cells by blocking ATP-sensitive potassium channels. Used for Type 2 diabetes mellitus.

At a glance

Generic nameComparator: glipizide
Also known asGlipizide
SponsorMerck Sharp & Dohme LLC
Drug classMeglitinide (rapid-acting insulin secretagogue)
TargetATP-sensitive potassium channel (KATP channel) / Sulfonylurea receptor
ModalitySmall molecule
Therapeutic areaDiabetes
PhasePhase 3

Mechanism of action

Glipizide is a meglitinide-class insulin secretagogue that binds to sulfonylurea receptors on the ATP-sensitive potassium channels in pancreatic beta cells. This binding closes the potassium channels, leading to cell depolarization and opening of voltage-gated calcium channels, which triggers insulin release. It is used to lower blood glucose in type 2 diabetes by increasing endogenous insulin secretion.

Approved indications

Common side effects

Key clinical trials

Primary sources

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