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After 40 weeks, the blood sugar levels of people receiving the drug had dropped by between 1.7% and 1.9% compared with 0.8% for people receiving a placebo
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G49, a dual glucagon/glucagon-like peptide-1 receptor agonist, triggers an inter-organ crosstalk between adipose tissue, pancreas and liver, leading to brown fat activation with the final outcomes of increased energy expenditure and body weight loss.
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