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The primary endpoint, NASH resolution without worsening fibrosis, was achieved in 39% of the liraglutide group, compared with 9% of the placebo group (relative risk [RR] = 4.3
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This strategy allowed insurers that didnt cover weight loss products to include the diabetes-indicated version on their drug formularies, while excluding the weight loss version
Epinephrine-induced insulin resistance in man
doi: 10.1210/en.2004-0015
comparison is placebo or antidiabetic
