2026-04-17T05:20:42Zhttps://recercat.cat/oai/request

oai:recercat.cat:2072/4413512024-10-31T05:14:40Zcom_2072_98col_2072_378192

00925njm 22002777a 4500 dc Armstrong, April W author Paul, Carle author Puig Sanz, Lluís author Boehncke, Wolf-Henning author Freeman, Michael author Torii, Hideshi author Papp, Kim author Griffiths, Christopher E. M. author Blauvelt, Andrew author Reich, Kristian author Gooderham, Melinda author Terui, Tadashi author Renda, Lisa author Agada, Noah author Xu, Wen author Gallo, Gaia author Lebwohl, Mark G. author Universitat Autònoma de Barcelona author 2019 Altres ajuts: The studies described herein and the Rapid Service Fee were funded by Eli Lilly and Company. Long-term safety data are critical for evaluating therapies for psoriasis. Ixekizumab has demonstrated efficacy and is well tolerated for the treatment of moderate-to-severe plaque psoriasis. We examined the safety and tolerability of up to 5 years of ixekizumab therapy in patients with psoriasis. Integrated safety data were analyzed from 13 ixekizumab clinical studies. Rates of treatment-emergent adverse events (TEAEs), serious AEs (SAEs) and AEs of special interest were analyzed for the 12-week induction period in the combined pivotal studies, and for all pooled studies by year(s) of therapy and overall, reported as exposure-adjusted incidence rates (IRs) per 100 patient-years (p-y) and/or frequencies. Total ixekizumab exposure was 17,003.4 p-y (N = 5898); 2749 patients had ≥ 4 years of exposure. When compared across years of exposure, rates for AEs remained largely stable or declined, including TEAEs leading to discontinuation (3.8/100 p-y in year 1, declining to 2.0/100 p-y in year 5); SAEs (range 6.2-7.0/100 p-y); serious infections (range 1.3-1.7/100 p-y); nonmelanoma skin cancer (ranging from 0.5/100 p-y in year 1 to 0.2/100 p-y in years 4-5); other malignancies (range 0.4-0.6/100 p-y); inflammatory bowel disease including ulcerative colitis and Crohn's disease (IR 0.2/100 p-y); and major adverse cardiovascular events (MACE) (range 0.3-0.7/100 p-y). Candidiasis was reported in 327 patients (IR 1.9/100 p-y), with the majority identified as mucocutaneous. The rate of injection site reactions was 15.5/100 p-y during year 1 and 2.0-2.3/100 p-y by years 3-5. The decrease in rates of TEAEs and the stable rates of SAEs, other malignancies and MACE during up to 5 years of ixekizumab dosing are consistent with previous reports describing a favorable safety profile of ixekizumab following shorter durations of exposure. Eli Lilly and Company. Adverse events Etanercept IL-17 Integrated analysis Ixekizumab Safety Psoriasis Safety of Ixekizumab Treatment for up to 5 Years in Adult Patients with Moderate-to-Severe Psoriasis : Results from Greater Than 17,000 Patient-Years of Exposure