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ARA-290 was engineered to retain those protective benefits while eliminating the blood cell stimulation that makes traditional EPO risky for non-anemic patients

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We used KaplanMeier analysis with Cox proportional-hazards regression for the time-to-event analysis to determine hazard ratios and 95% confidence intervals for major adverse cardiovascular events

Baseline labs should be drawn before starting therapy, with follow-up testing at 8-12 weeks to assess response and guide dose adjustments

Samples were stored at 80 C for up to 2 weeks