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pramlintide acetate (Symlin)

AstraZeneca · FDA-approved active Small molecule Under review

pramlintide acetate (Symlin) is a Amylin receptor agonist Small molecule drug developed by AstraZeneca. It is currently FDA-approved for Type 1 diabetes mellitus (adjunct to insulin therapy), Type 2 diabetes mellitus (adjunct to insulin therapy). Also known as: Symlin.

Pramlintide is a synthetic analog of amylin that slows gastric emptying, suppresses glucagon secretion, and promotes satiety to reduce postprandial glucose excursions in diabetes.

Pramlintide acetate, also known as Symlin, is a protein-based agonist that targets the amylin receptor AMY1, CALCR/RAMP1. It is used to treat various conditions, including diabetes mellitus, type 1 diabetes, type 2 diabetes, and obesity, as studied in clinical trials.

At a glance

Generic namepramlintide acetate (Symlin)
Also known asSymlin
SponsorAstraZeneca
Drug classAmylin receptor agonist
TargetAmylin receptor (calcitonin receptor-like receptor with receptor activity-modifying protein 3)
ModalitySmall molecule
Therapeutic areaDiabetes
PhaseFDA-approved

Mechanism of action

Pramlintide mimics the natural hormone amylin, which is co-secreted with insulin by pancreatic beta cells. It acts on amylin receptors to modulate three key postprandial processes: delaying stomach emptying to slow nutrient absorption, inhibiting glucagon release to prevent hepatic glucose production, and enhancing satiety signals to reduce food intake. These combined effects lower postmeal blood glucose spikes in patients with type 1 and type 2 diabetes.

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

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Frequently asked questions about pramlintide acetate (Symlin)

What is pramlintide acetate (Symlin)?

pramlintide acetate (Symlin) is a Amylin receptor agonist drug developed by AstraZeneca, indicated for Type 1 diabetes mellitus (adjunct to insulin therapy), Type 2 diabetes mellitus (adjunct to insulin therapy).

How does pramlintide acetate (Symlin) work?

Pramlintide is a synthetic analog of amylin that slows gastric emptying, suppresses glucagon secretion, and promotes satiety to reduce postprandial glucose excursions in diabetes.

What is pramlintide acetate (Symlin) used for?

pramlintide acetate (Symlin) is indicated for Type 1 diabetes mellitus (adjunct to insulin therapy), Type 2 diabetes mellitus (adjunct to insulin therapy).

Who makes pramlintide acetate (Symlin)?

pramlintide acetate (Symlin) is developed and marketed by AstraZeneca (see full AstraZeneca pipeline at /company/astrazeneca).

Is pramlintide acetate (Symlin) also known as anything else?

pramlintide acetate (Symlin) is also known as Symlin.

What drug class is pramlintide acetate (Symlin) in?

pramlintide acetate (Symlin) belongs to the Amylin receptor agonist class. See all Amylin receptor agonist drugs at /class/amylin-receptor-agonist.

What development phase is pramlintide acetate (Symlin) in?

pramlintide acetate (Symlin) is FDA-approved (marketed).

What are the side effects of pramlintide acetate (Symlin)?

Common side effects of pramlintide acetate (Symlin) include Nausea, Vomiting, Anorexia, Hypoglycemia, Headache, Abdominal pain.

What does pramlintide acetate (Symlin) target?

pramlintide acetate (Symlin) targets Amylin receptor (calcitonin receptor-like receptor with receptor activity-modifying protein 3) and is a Amylin receptor agonist.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing