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Cellular Sequence

Peptide Encyclopaedia

Approved medicineApproved medicine

Pramlintide

Also known as Symlin.

Approved-medicine listing only. This is not available from the Cellular Sequence shop. Licensed products require a prescriber and an ARTG-registered presentation.

At-a-glance profile

Classification
Amylin analogue
Approval status
Approved medicine
Research status
Labelled indications are defined in product information.
Molecular formula
Insufficient reliable evidence identified.
Molecular weight
Insufficient reliable evidence identified.
Sequence
Synthetic analogue of human amylin (islet amyloid polypeptide).
Primary biological target
Amylin receptors (calcitonin-receptor complexes)
Half-life
Insufficient reliable evidence identified.
Routes investigated
Subcutaneous
Human evidence level
A — Approved clinical use / strong human evidence

What is it?

An approved adjunct peptide injection for selected insulin-treated diabetes, as labelled.

Mechanism of action

Established (labelled / textbook receptor pharmacology)

Amylin-receptor agonism slows gastric emptying, suppresses post-prandial glucagon and promotes satiety.

Reduces post-prandial glucose excursions when used as labelled with insulin — hypoglycaemia risk requires insulin down-titration per PI.

What is it being studied for?

  • Type 1 diabetes adjunct
  • Insulin-treated type 2 diabetes

Investigational findings are not proven clinical benefits unless an authority has labelled that indication.

Evidence level

Overall human evidence grade: A · Approved clinical use / strong human evidence

Human research

Labelled clinical programme for Symlin.

Preclinical research

Animal, cell and in-vitro findings are listed separately from human effects.

Amylin physiology is established.

Doses reported in published research

This section does not provide personalised medical dosing. Values are those reported in papers or protocols. Animal mg/kg doses are not converted to human doses.

Doses reported in human studies

Insufficient reliable evidence identified.

Preclinical / animal study dosing

Insufficient reliable evidence identified.

Pharmacokinetics

Reliable human pharmacokinetic data were not identified for this encyclopaedia entry, or are limited to product information for approved presentations.

Safety

Nausea; severe hypoglycaemia when insulin is not reduced as labelled.

Unknowns. Absence of a published harm signal is not evidence of safety.

Contraindications. Gastroparesis, hypoglycaemia unawareness — see PI.

Regulatory status

FDA-approved (Symlin). Confirm other agencies.

Verify ARTG; not sold here.

Citations

  1. [1] Symlin (pramlintide) prescribing information

    Symlin (pramlintide) prescribing information

    Open source

For educational and research reference only. This page summarises published scientific literature and does not constitute medical advice, prescribing information or a recommendation to use an investigational compound. Research doses shown describe doses reported in published studies and are not personalised dosing instructions.

Last reviewed 2026-09-13. Research areas: Metabolic · Compare peptides