FDA Drug Label
SAXENDA (liraglutide) injection — Prescribing Information
Novo, 2014
Victoza / Saxenda
Liraglutide (Victoza for T2D, Saxenda for obesity) is Novo Nordisk's FDA-approved once-daily injectable GLP-1 receptor agonist. SCALE obesity trial demonstrated 5–8% body weight reduction and significant HbA1c reduction. While largely superseded by once-weekly semaglutide and tirzepatide for weight loss, Liraglutide remains a cornerstone type 2 diabetes treatment and has a robust cardiovascular outcomes trial (LEADER) demonstrating cardiovascular risk reduction.
Trend index
Overview
Liraglutide (Victoza for T2D, Saxenda for obesity) is Novo Nordisk's FDA-approved once-daily injectable GLP-1 receptor agonist. SCALE obesity trial demonstrated 5–8% body weight reduction and significant HbA1c reduction. While largely superseded by once-weekly semaglutide and tirzepatide for weight loss, Liraglutide remains a cornerstone type 2 diabetes treatment and has a robust cardiovascular outcomes trial (LEADER) demonstrating cardiovascular risk reduction.
Community
Positive 100% · Neutral 0% · Negative 0%
Median: 2000+ mcg · Most common: 2000+ mcg
Research
FDA Drug Label
Novo, 2014
FDA Drug Label
Novo, 2010
PubMed
Marso et al., 2016
PubMed
Pi-Sunyer et al., 2015
Help
This page summarizes 6 anonymized self-reports from PeptIQ users who track Liraglutide, including commonly reported effects and co-tracked peptides. These are observational patterns, not clinical outcomes.
4 sources are linked on this page, including PubMed articles, clinical trial registries, and FDA labels where applicable. Citations describe published research — not recommendations.
This wiki does not assess safety or recommend use. Liraglutide is listed as FDA Approved. Consult a licensed clinician for personal medical decisions.
Research, primarily in animal models, suggests Liraglutide 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.
SourceLiraglutide 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 Liraglutide as a Category 2 bulk drug substance, which explicitly prohibits licensed compounding pharmacies from using it in compounded medications.
SourceThe safety and effectiveness of Liraglutide 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.
SourceWhile there are over 200 published studies on Liraglutide, 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