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9 months. Siprosan cytodrox cardiovascular events occurred in 61 of 1,591 patients 3. 8 in the oral semaglutide group and in 76 of 1,592 4. 8 in the control group hazard ratio, 0. 79; 95 CI.0. 57 to 1. 11; P 0. 001 for noninferiority. The results for the components of the primary outcome measure were as follows death from cardiovascular causes, 15 of 1,591 patients 0. 9 in the oral semaglutide group and 30 of Cytodrox 1. 9 in the placebo group ratio risk ratio, 0. 49; 95 CI, 0. 27 to 0. 92; nonfatal myocardial infarction, 37 of 1,591 2.

3 and 31 of 1,592 1. 9, respectively hazard ratio, 1. 18; 95 CI, 0. 73 to 1. 90; and nonfatal stroke, 12 of 1,591 0.