Peptide Encyclopaedia
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] Symlin (pramlintide) prescribing information
Symlin (pramlintide) prescribing information
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