Last reviewed · How we verify

Glimepiride or gliclazide

Merck Sharp & Dohme LLC · Phase 3 active Small molecule

Glimepiride and gliclazide stimulate insulin secretion from pancreatic beta cells by blocking ATP-sensitive potassium channels.

Glimepiride and gliclazide stimulate insulin secretion from pancreatic beta cells by blocking ATP-sensitive potassium channels. Used for Type 2 diabetes mellitus.

At a glance

Generic nameGlimepiride or gliclazide
SponsorMerck Sharp & Dohme LLC
Drug classSulfonylurea
TargetATP-sensitive potassium channel (KATP channel) / Sulfonylurea receptor
ModalitySmall molecule
Therapeutic areaDiabetes
PhasePhase 3

Mechanism of action

Both drugs are second-generation sulfonylureas that bind to sulfonylurea receptors on the ATP-sensitive potassium channels in pancreatic beta cells. This binding closes the channels, depolarizes the cell membrane, and triggers calcium influx, which stimulates the release of stored insulin. This mechanism lowers blood glucose in patients with type 2 diabetes by increasing endogenous insulin secretion.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: