Pramlintide
Also known as: Symlin, Pramlintida, Acetato de Pramlintida
Molecular Identifiers
Molecular Formula
C171H267N51O53S2
CAS Number
151126-32-8
PubChem CID
70691388Molecular Weight
3949.4 Da
Overview
Synthetic analog of human amylin, with a molecular weight of approximately 3,949.4 Da. Amylin is a hormone co-secreted with insulin by pancreatic beta cells. Pramlintide has proline substitutions at positions 25, 28, and 29, providing superior solubility and stability compared to the native peptide. Approved as an adjunct to insulin in the treatment of type 1 and type 2 diabetes.
Approved by the FDA as Symlin (2005) as adjunctive therapy to insulin for patients with type 1 and type 2 diabetes who do not achieve adequate glycemic control with insulin alone.
Clinical interest in pramlintide centers on postprandial hyperglycemia control in type 1 and type 2 diabetic patients who do not reach glycemic targets on insulin alone. It acts through a mechanism complementary to insulin — delaying gastric emptying, suppressing inappropriate postprandial glucagon, and increasing satiety — leading to reduced glycemic excursion and modest weight loss as an added benefit.
It was FDA-approved in 2005 as Symlin, indicated as adjunctive therapy to prandial insulin. It is prescribed exclusively in an endocrinology setting, in a pre-filled pen, with mandatory escalation (T1D: 15→30→45→60 mcg; T2D: 60→120 mcg) and compulsory 50% reduction of prandial insulin dose at initiation to avoid severe hypoglycemia. It is not mixed with insulin in the same syringe.
Endogenous amylin, from which pramlintide is derived, was identified in pancreatic islet amyloid deposits in type 2 diabetics in the 1980s, which led to the development of a soluble analog with proline substitutions at positions 25, 28, and 29 to overcome the aggregation tendency of the native peptide.
Within the amylin family, it is the short-acting, prandial analog — a counterpoint to cagrilintide (a long-acting amylin with weekly dosing). While pramlintide acts specifically on postprandial glycemic excursion control as an adjunct to insulin, cagrilintide is positioned as a chronic weight management tool, generally combined with semaglutide (CagriSema).
KCNTATCATQRLANFLVHSSNNFGPILPPTNVGSNTY Lys-Cys-Asn-Thr-Ala-Thr-Cys-Ala-Thr-Gln-Arg-Leu-Ala-Asn-Phe-Leu-Val-His-Ser-Ser-Asn-Asn-Phe-Gly-Pro-Ile-Leu-Pro-Pro-Thr-Asn-Val-Gly-Ser-Asn-Thr-Tyr Half-life
~48 minutes
Administration Route
Subcutaneous
Category
Metabolic & Fat Loss
Mechanism of Action
- Amylin receptor agonism (AMY1, AMY2, AMY3)
- Delayed postprandial gastric emptying
- Suppression of inappropriate postprandial glucagon secretion
- Promotion of satiety via signaling in the area postrema and nucleus of the solitary tract
- Reduction of postprandial glycemic excursion
- Body weight modulation through decreased caloric intake
Dosage Protocol
Data compiled from the literature. This does not constitute medical advice.
| Parameter | Value |
|---|---|
| Dose | 15-120 mcg per injection (subcutaneous) |
| Frequency | Before main meals (2-3 times daily) |
| Timing | Immediately before meals with 250+ calories |
| Duration | Continuous use (with gradual escalation) |
Reported Side Effects
Adverse effects described in the literature. Severity and frequency vary between individuals.
- Nausea
- Hypoglycemia
- Anorexia
- Vomiting
- Headache
- Abdominal pain
Product Properties
| Purity | >99% |
| Appearance | White lyophilized powder |
| Solubility | Soluble in water and bacteriostatic water |
| Source | Solid-phase peptide synthesis (SPPS) |
| Storage | Lyophilized: -20°C for up to 2 years, 2-8°C for up to 6 months. Reconstituted: 2-8°C for up to 30 days. Protect from light and moisture. Avoid repeated freeze-thaw cycles. |
Presentations & Preparation
Vials of Pramlintide found in the research market:
Reconstitution
- Diluent: Available as a ready-to-use pen solution
- Volume: Pre-filled pen of 1.5 ml (1000 mcg/ml)
- Use pre-filled pen — no reconstitution required
- Inject subcutaneously in the abdomen or thigh, rotating sites
- Start with a low dose (15 mcg T1D or 60 mcg T2D) and escalate gradually
- Reduce prandial insulin dose by 50% when initiating pramlintide
Storage
- Lyophilized: Not applicable — ready-to-use solution
- Reconstituted: Refrigerated 2-8°C (unopened); room temperature up to 30 days (in use)
- Do not freeze
- Protect from direct light
- Discard pen after 30 days of use even if not empty
Scientific Studies
Published studies on Pramlintide.
Progressive reduction in body weight after treatment with the amylin analog pramlintide in obese subjects: a phase 2, randomized, placebo-controlled, dose-escalation study
Aronne L, Fujioka K, Aroda V, Chen K, Halseth A, Kesty NC, et al.
Pramlintide as an Adjunct to Insulin Therapy Improves Long-Term Glycemic and Weight Control in Patients With Type 2 Diabetes
Hollander PA, Levy P, Fineman MS, Maggs DG, Shen LZ, Strobel SA, et al.
Related Peptides
5-Amino-1MQ
50 mg per capsule · 1-2 times daily
Adipotide
0.03 mg/kg body weight (Phase 1 trial starting dose) · Once daily
AICAR
0.1 mg/kg/min by intravenous infusion (CABG trial dose) · Single continuous infusion
AOD 9604
300-600 mcg per injection · Once daily
Cagrilintide
1.2-4.5 mg per week (subcutaneous) · Once weekly
Dulaglutide
0.75-4.5 mg per week (subcutaneous) · Once weekly