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Investor Presentaiton

CSL112 Apolipoprotein A-I (human) - AEGIS-II Objective: to evaluate the efficacy and safety of CSL112 on reducing the risk of cardiovascular (CV) death, myocardial infarction (MI), or stroke Treatment period (4 weekly infusions) 6 g CSL112 (n=9,112) Follow-up period (1 year) 18,219 MI patients from 49 Countries Infusion: Placebo (n=9,107) 1 2 3 2 3 4 5 6 7 8 9 10 11 8 15 22 29 60 90 180 270 365 Visit: 1 Study day: Within 5 days of arriving for evaluation and treatment of MI Randomization Driven by Our Promise 11 All infusions given within 30 days of the first infusion Primary Endpoint at 90 days Time to first occurrence of any component of the composite endpoint of CV death, MI, or stroke from time of randomization through 90 days CSL
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