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The drug is a mammalian oxyntomodulin analogue , activating both GLP-1 and glucagon receptors , thereby promoting insulin secretion, enhancing fat metabolism, and increasing energy expenditure

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In a recent interview, Patricia Grigson, one of the lead investigators, said: The GLP-1 drugs reduced craving beginning with the lowest dose of liraglutide, even when patients were reporting high levels of stress

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