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Comparator: glimepiride

Merck Sharp & Dohme LLC · FDA-approved active Small molecule

Glimepiride stimulates insulin secretion from pancreatic beta cells by binding to sulfonylurea receptors on the cell membrane.

Glimepiride stimulates insulin secretion from pancreatic beta cells by binding to sulfonylurea receptors on the cell membrane. Used for Type 2 diabetes mellitus.

At a glance

Generic nameComparator: glimepiride
Also known asAmaryl®
SponsorMerck Sharp & Dohme LLC
Drug classSulfonylurea
TargetSulfonylurea receptor (SUR1) / ATP-sensitive potassium channel
ModalitySmall molecule
Therapeutic areaDiabetes
PhaseFDA-approved

Mechanism of action

Glimepiride is a meglitinide-class sulfonylurea that closes ATP-sensitive potassium channels in pancreatic beta cells, leading to cell depolarization and calcium influx, which triggers insulin release. This mechanism helps lower blood glucose in patients with 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

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