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Symlin (pramlintide)

Baylor College of Medicine · FDA-approved active Small molecule

Pramlintide is an amylin analog that slows gastric emptying, reduces postprandial glucagon secretion, and increases satiety to improve blood glucose control in diabetes.

Pramlintide is an amylin analog that slows gastric emptying, reduces postprandial glucagon secretion, and increases satiety to improve blood glucose control in diabetes. Used for Type 1 diabetes mellitus (adjunct to insulin therapy), Type 2 diabetes mellitus (adjunct to insulin therapy).

At a glance

Generic nameSymlin (pramlintide)
SponsorBaylor College of Medicine
Drug classAmylin analog
TargetAmylin receptor
ModalitySmall molecule
Therapeutic areaDiabetes
PhaseFDA-approved

Mechanism of action

Pramlintide mimics amylin, a hormone co-secreted with insulin that regulates postprandial glucose excursions. It acts on amylin receptors to delay gastric emptying, suppress glucagon secretion during the postprandial period, and promote satiety. These combined effects reduce postmeal blood glucose spikes in patients with type 1 and 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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