GLP-1 & MetabolicPhase 3 ProgramS

Cagrilintide

AM833

Long-acting amylin analog studied for obesity and metabolic disease.

Observational report only — live community data. Not medical advice. Does not recommend doses, protocols, or treatments.
Studies cited
3
Research grade
S
Community score
183

Trend index

Trackers
4,031

Overview

About Cagrilintide

Long-acting amylin analog studied for obesity and metabolic disease.

Category
GLP-1 & Metabolic
Regulatory status
Phase 3 Program
Also known as
AM833
Self-reports
29

Community

What 29 users report

29 community reports

Positive 98% · Neutral 2% · Negative 0%

Most reported benefits

Appetite
139

Most reported side effects

Nausea
1
Digestive upset
1
Injection site irritation
1

Dose distribution

Median: 2000+ mcg · Most common: 2000+ mcg

0–25
41
25–50
0
50–100
0
100–200
0
200–400
9
400–600
2
600–1000
3
1000–2000
1
2000+
83

How repeat users are trending

Among repeat reporters, 87% said they felt similar to their last entry, 13% more positive, and 0% more negative.

Overall, repeat reporters leaned more positive than their previous entry.

Median gap between entries: 142 days · Based on 23 repeat reporters

Research

Cited research (2)

Help

Frequently asked

What do PeptIQ users report about Cagrilintide?

This page summarizes 29 anonymized self-reports from PeptIQ users who track Cagrilintide, including commonly reported effects and co-tracked peptides. These are observational patterns, not clinical outcomes.

What research is cited for Cagrilintide?

2 sources are linked on this page, including PubMed articles, clinical trial registries, and FDA labels where applicable. Citations describe published research — not recommendations.

Is Cagrilintide safe to use?

This wiki does not assess safety or recommend use. Cagrilintide is listed as Phase 3 Program. Consult a licensed clinician for personal medical decisions.

What are the purported benefits and uses of Cagrilintide?

Research, primarily in animal models, suggests Cagrilintide may have a wide range of therapeutic potentials due to its ability to promote angiogenesis (formation of new blood vessels), stimulate collagen synthesis, and modulate inflammatory responses.

Source

What is the legal status of Cagrilintide?

Cagrilintide is not approved by the FDA for any human use. There is no legal basis for selling it as a drug, food, or dietary supplement in the United States. The FDA has classified Cagrilintide as a Category 2 bulk drug substance, which explicitly prohibits licensed compounding pharmacies from using it in compounded medications.

Source

What are the known or theoretical side effects and risks of Cagrilintide?

The safety and effectiveness of Cagrilintide have not been thoroughly evaluated in humans through rigorous clinical trials. This lack of human data means that safe dosages, short-term side effects, and long-term health consequences are largely unknown.

Source

What is the current state of research on Cagrilintide?

While there are over 200 published studies on Cagrilintide, the vast majority are animal or in vitro (cell) studies. These preclinical studies consistently show positive results across various tissue types. However, there is a significant lack of comprehensive human clinical trial data.

Source