Research

Hormonal

Daily subcutaneous administration of the dual GLP-1/glucagon receptor agonist MEDI0382 produces superior weight loss and fat mass reduction in diet-induced obese mice and cynomolgus monkeys compared to the GLP-1 analogue liraglutide, driven by glucagon receptor-mediated increases in energy expenditure.

For individuals seeking significant weight loss and metabolic improvement, dual GLP-1/glucagon receptor agonists like MEDI0382 offer superior fat loss compared to GLP-1-only treatments. This is achieved through daily subcutaneous injections that leverage both satiety signals (GLP-1) and increased energy expenditure (glucagon). While effective in animal models, human clinical application requires medical supervision due to the hormonal nature of the intervention.

GoodSupportsHIGH confidence
MEDI0382 produced superior weight loss and comparable glucose lowering to the GLP-1 peptide analogue liraglutide when administered daily at comparable doses in DIO mice. The additional fat mass reduction elicited by MEDI0382 probably results from a glucagon receptor-mediated increase in energy expenditure, whereas food intake suppression results from activation of the GLP-1 receptor.
Susan Henderson et al. · Diabetes Obesity and Metabolism · 2016

Why this rating

High-quality preclinical data in both rodents and non-human primates, though not human clinical trials.

Source

Robust anti‐obesity and metabolic effects of a dual <scp>GLP</scp> ‐1/glucagon receptor peptide agonist in rodents and non‐human primates

Susan Henderson et al. · Diabetes Obesity and Metabolism · 2016

DOI 10.1111/dom.12735

mechanism_onlyCited 235×
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DOI resolved against Crossref · corpus check 2026-06-10

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