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Peptide Profile

Pramlintide

Symlin · AC0137

Pramlintide is a synthetic analogue of the pancreatic hormone amylin, approved by the FDA as an adjunct to insulin therapy in adults with type 1 or type 2 diabetes, and investigated for weight management due to amylin's central…

MetabolicFDA ApprovedPrescription
Used forfat loss
Half-life
~48 minutes
Routes
subcutaneous

Educational research information — not medical advice. Review primary sources and consult a qualified professional before any decision.

Educational research tools — not medical advice.

Overview

What Pramlintide is

About Pramlintide

Synthetic amylin analogue; activates amylin receptors in hypothalamus; slows gastric emptying, suppresses glucagon, enhances satiety

Pramlintide is a synthetic analogue of the pancreatic hormone amylin, approved by the FDA as an adjunct to insulin therapy in adults with type 1 or type 2 diabetes, and investigated for weight management due to amylin's central role in meal-related satiety signaling. Amylin is co-secreted with insulin from pancreatic beta-cells and slows gastric emptying, suppresses post-meal glucagon release, and activates satiety circuits in the area postrema and nucleus tractus solitarius of the brainstem. Randomized controlled trials demonstrate that subcutaneous pramlintide administration before meals significantly reduces 24-hour caloric intake, meal sizes, and body weight in obese subjects, with effects independent of glycemic control. Pramlintide is an FDA-approved prescription medication (Symlin); its weight management application is off-label in non-diabetic patients, and use requires monitoring for hypoglycemia, particularly when co-administered with insulin. Pramlintide vs cagrilintide: the amylin analogue generation gap Pramlintide (Symlin) is a first-generation amylin analogue with a short half-life requiring injection before each meal. Per FDA labeling, the maintenance dose is 30–60 mcg per meal for type 1 diabetes and 120 mcg per meal for type 2 diabetes. Cagrilintide, currently in Phase 3 development, is a long-acting amylin analogue designed for once-weekly subcutaneous administration, combining with semaglutide in the CagriSema combination. Cagrilintide's weekly dosing removes this barrier and enables combination with a weekly GLP-1 agonist in a single injection protocol. Pramlintide for weight management: In adults without diabetes, pramlintide produces modest mean weight reductions of 3–5% over 6-month studies — less than GLP-1 agonists but with a complementary mechanism. Some researchers have combined pramlintide with a GLP-1 agonist (pramlintide + GLP-1) as an early-generation dual amylin/incretin approach, reporting additive weight reductions. CagriSema (cagrilintide + semaglutide) in Phase 3 represents the pharmacologically optimised version of this dual approach, with superior efficacy and weekly dosing. Pramlintide's practical role in new weight management programs has therefore narrowed significantly as cagrilintide and GLP-1/amylin combinations approach approval.

Pramlintide Benefits & Research Areas

appetite suppressionpostprandial glucose controlweight lossgastric emptying delay

Research Signals

Population research notes

30s40s50+

These signals reflect research interest areas, not treatment indications.

Pharmacokinetics

Pramlintide half-life calculator

Compound & timing

Half-lifefrom PeptideBase data
Source: "~48 minutes" · Pramlintide (PeptideBase)
to show amount remaining
48 min
0%25%50%75%100%050100150200250time since dose (min)
Plasma decay curve for Pramlintide: 50% remaining at 48 min after the dose.
plasma level
50%remaining in plasmaat 48 min after the dose
Half-life
48 min
~97% cleared after
4 h

Model: single-dose, first-order (single-compartment) estimate. Real clearance is multi-compartment and varies by individual and route.

The Research

What the evidence says about Pramlintide

Research Evidence

based on 3 studies · 2 RCTs · most recent 2026

Regulatory Status

Availability Status
Prescription
FDA Status
FDA Approved
Effective Date
March 16, 2005

FDA-approved amylin analog. Brand: Symlin (NDA 021332, Mar 2005). Adjunct to insulin therapy in T1D and T2D. Prescription only. Subcutaneous injection.

Regulatory status reflects publicly available information and may change. This is not legal or medical advice.

Research Sources

3 sources cited · 2 strong · 1 weak

2 RCTs · 1 In vitro

  • Pramlintide combined with metreleptin in obesity: sustained reductions in weight, metabolic markers, and leptin requirements

    Obesity · 2009

    Research in a 24-week combination trial found that pramlintide plus metreleptin produced a mean body weight reduction of 12.7% compared with 8.4% for pramlintide alone and 8.2% for metreleptin alone in obese adults, suggesting synergistic satiety effects from dual amylin and leptin receptor engagement.

    RCTn=177StrongPMID 19521351
  • Pramlintide reduced 24-h caloric intake and increased satiety in obese subjects: a randomized, double-blind, dose-response study

    American Journal of Physiology: Endocrinology and Metabolism · 2007

    Research in an 8-week dose-response trial found that subcutaneous pramlintide reduced 24-hour caloric intake by 680 to 990 kcal and produced mean body weight reduction of 2.1% compared with a 0.1% gain in placebo-treated obese adults, supporting its role as a satiety-promoting agent.

    RCTn=88StrongPMID 17505051
  • In vitro metabolic profiling of weight-loss-inducing amylin receptor agonists in the context of preventive doping research.

    J Pharm Biomed Anal · 2026

    In vitroWeakPMID 41702251

Pramlintide Side Effects & Safety Considerations

Research-use compound with limited human data. Evidence strength varies — see the Evidence section.

Reported (unverified — pending clinical review)

hypoglycemia unawarenessgastroparesis

No established clinical contraindications

Common monitoring markers in research protocols

Under clinical review

Being verified by our medical team before we display monitoring guidance for this peptide.

Consult a qualified healthcare professional before making any health decisions. This information is educational only and does not constitute medical advice.

Frequently Asked Questions — Pramlintide

Pramlintide is a synthetic analogue of the pancreatic hormone amylin, approved by the FDA as an adjunct to insulin therapy in adults with type 1 or type 2 diabetes, and investigated for weight management due to amylin's central role in meal-related satiety signaling. Amylin is co-secreted with insulin from pancreatic beta-cells and slows gastric emptying, suppresses post-meal glucagon release, and activates satiety circuits in the area postrema and nucleus tractus solitarius of the brainstem.

appetite suppression, postprandial glucose control, weight loss, gastric emptying delay.

Research on Pramlintide primarily documents effects related to appetite suppression and postprandial glucose control and weight loss and gastric emptying delay. These are areas covered in preclinical and clinical literature — individual response varies and effects depend on context of use.

Reported contraindications and considerations for Pramlintide include hypoglycemia unawareness, gastroparesis. This is educational information only — consult a qualified healthcare professional before use.

For Pramlintide, its FDA status is FDA-approved, and it is available by prescription. Regulatory status reflects publicly available information and may change. This is not legal or medical advice.

Research in a 24-week combination trial found that pramlintide plus metreleptin produced a mean body weight reduction of 12.7% compared with 8.4% for pramlintide alone and 8.2% for metreleptin alone in obese adults, suggesting synergistic satiety effects from dual amylin and leptin receptor engagement.

Access

How to get Pramlintide

Where to buy Pramlintide

Coverage expanding

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