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DOI: 10.1007/s00125-010-2028-x [Google Scholar] Jia Y, Zheng Z, Guan M, Zhang Q, Li Y, Wang L, et al
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The SURPASS-CVOT trial, where dulaglutide at the dose of 1.5 mg/week or at the highest tolerated dose, is the comparator, has a distinctive design from the other trials: the primary endpoint is the time to the first manifestation of any major adverse CV event (MACE), defined as myocardial infarction, stroke or CV death
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