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ABSTRACT: Purpose
Patients with polyvascular disease (PVD) are at very high cardiovascular risk and require intensive lipid-lowering therapy. This analysis describes the lipid-lowering efficacy and safety of inclisiran versus placebo in patients with and without PVD.Methods
In this post hoc analysis of the ORION-9, ORION-10, and ORION-11 trials, patients were randomized 1:1 to receive 284 mg inclisiran (300 mg inclisiran sodium) or placebo on day 1, day 90, and 6-monthly thereafter. Percentage change in low-density lipoprotein cholesterol (LDL-C) from baseline to day 510 and corresponding time-adjusted change from day 90 and up to day 540 were evaluated per patients' PVD status. Safety was assessed over 540 days.Results
Of 3454 patients, 470 (13.6%) had PVD, and 2984 (86.4%)
SUBMITTER: Koenig W
PROVIDER: S-EPMC11101568 | biostudies-literature | 2024 Jun
REPOSITORIES: biostudies-literature