Leiter, Lawrence ACariou, BertrandMüller-Wieland, DirkColhoun, Helen MDel Prato, StefanoTinahones, Francisco JRay, Kausik KBujas-Bobanovic, MajaDomenger, CatherineMandel, JonasSamuel, RitaHenry, Robert R2023-01-252023-01-252017-10-10http://hdl.handle.net/10668/11579To investigate the efficacy and safety of alirocumab in participants with type 2 (T2D) or type 1 diabetes (T1D) treated with insulin who have elevated LDL cholesterol levels despite maximally tolerated statin therapy. Participants at high cardiovascular risk with T2D (n = 441) or T1D (n = 76) and LDL cholesterol levels ≥1.8 mmol/L (≥70 mg/dL) were randomized 2:1 to alirocumab:placebo administered subcutaneously every 2 weeks, for 24 weeks' double-blind treatment. Alirocumab-treated participants received 75 mg every 2 weeks, with blinded dose increase to 150 mg every 2 weeks at week 12 if week 8 LDL cholesterol levels were ≥1.8 mmol/L. Primary endpoints were percentage change in calculated LDL cholesterol from baseline to week 24, and safety assessments. Alirocumab reduced LDL cholesterol from baseline to week 24 by a mean ± standard error of 49.0% ± 2.7% and 47.8% ± 6.5% vs placebo (both P Alirocumab produced significant LDL cholesterol reductions in participants with insulin-treated diabetes regardless of diabetes type, and was generally well tolerated. Concomitant administration of alirocumab and insulin did not raise any safety concerns (NCT02585778).enAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/cardiovascular diseaseclinical triallipid-lowering therapytype 1 diabetestype 2 diabetesAgedAged, 80 and overAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAnticholesteremic AgentsCardiovascular DiseasesDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2Diabetic AngiopathiesDiabetic CardiomyopathiesDouble-Blind MethodDrug Administration ScheduleDrug ResistanceFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsHypercholesterolemiaHypoglycemic AgentsInjections, SubcutaneousInsulinMaleMiddle AgedRiskresearch article28905478open access10.1111/dom.131141463-1326PMC5698740https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/dom.13114https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698740/pdf