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Gliclazide (Comparison drug)

University of Glasgow · FDA-approved active Small molecule

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

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

At a glance

Generic nameGliclazide (Comparison drug)
SponsorUniversity of Glasgow
Drug classSulfonylurea
TargetATP-sensitive potassium channel (KATP channel)
ModalitySmall molecule
Therapeutic areaDiabetes
PhaseFDA-approved

Mechanism of action

Gliclazide is a meglitinide-class sulfonylurea that binds to ATP-sensitive potassium channels on pancreatic beta cells, causing cell depolarization and opening of voltage-gated calcium channels. This influx of calcium triggers the release of stored insulin into the bloodstream, thereby lowering blood glucose levels in patients with type 2 diabetes.

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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