PMID- 37604638 OWN - NLM STAT- MEDLINE DCOM- 20230823 LR - 20230912 IS - 2056-5933 (Electronic) IS - 2056-5933 (Linking) VI - 9 IP - 3 DP - 2023 Aug TI - Safety profile of baricitinib in patients with systemic lupus erythematosus: an integrated analysis. LID - 10.1136/rmdopen-2023-003302 [doi] LID - e003302 AB - OBJECTIVES: To assess the safety of the oral Janus kinase inhibitor baricitinib in adult patients with systemic lupus erythematosus (SLE) receiving stable background therapy. Topics of special interest included infections and cardiovascular and thromboembolic events. METHODS: This analysis included integrated safety data from three randomised, placebo-controlled studies (one phase 2 and two phase 3) and one long-term extension study. Data are reported in three data sets: placebo-controlled, extended exposure and all-baricitinib. Outcomes include treatment-emergent adverse events (AEs), AEs of special interest and abnormal laboratory changes. Proportions of patients with events and incidence rates (IRs) were calculated. RESULTS: A total of 1655 patients received baricitinib for up to 3.5 years (median duration 473 days). With baricitinib 4 mg, baricitinib 2 mg and placebo, respectively, 50.8%, 50.7% and 49.0% of patients reported at least one infection and 4.4%, 3.4% and 1.9% of patients had a serious infection. The most common treatment-emergent infections included urinary tract infection, COVID-19, upper respiratory tract infection and nasopharyngitis. Herpes zoster was more common with baricitinib 4 mg (4.7%) vs baricitinib 2 mg (2.7%) and placebo (2.8%). Among baricitinib-4 mg, 2 mg and placebo-treated patients, respectively, 4 (IR=0.9), 1 (IR=0.2) and 0 experienced at least one positively adjudicated major adverse cardiovascular event, and 0, 3 (IR=0.6) and 2 (IR=0.4) reported at least one positively adjudicated venous thromboembolism. CONCLUSIONS: The results of this integrated safety analysis in patients with SLE are not substantially different to the established safety profile of baricitinib. No increased venous thromboembolism was found. CI - (c) Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. FAU - Morand, Eric AU - Morand E AUID- ORCID: 0000-0002-9507-3338 AD - Centre for Inflammatory Disease, Monash University, Melbourne, VIC, Australia eric.morand@monash.edu. FAU - Smolen, Josef S AU - Smolen JS AD - Medical University of Vienna, Vienna, Austria. FAU - Petri, Michelle AU - Petri M AD - Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, USA. FAU - Tanaka, Yoshiya AU - Tanaka Y AUID- ORCID: 0000-0002-0807-7139 AD - University of Occupational and Environmental Health, Japan, Kitakyushu, Japan. FAU - Silk, Maria AU - Silk M AD - Eli Lilly and Company, Indianapolis, Indiana, USA. FAU - Dickson, Christina AU - Dickson C AD - Eli Lilly and Company, Indianapolis, Indiana, USA. FAU - Meszaros, Gabriella AU - Meszaros G AD - Eli Lilly and Company, Indianapolis, Indiana, USA. FAU - de la Torre, Inmaculada AU - de la Torre I AD - Eli Lilly and Company, Indianapolis, Indiana, USA. FAU - Issa, Maher AU - Issa M AD - Eli Lilly and Company, Indianapolis, Indiana, USA. FAU - Zhang, Hong AU - Zhang H AD - TechData Service, King of Prussia, Pennsylvania, USA. FAU - Dorner, Thomas AU - Dorner T AUID- ORCID: 0000-0002-6478-7725 AD - Department of Rheumatology and Clinical Immunology, Charite Universitatsmedizin Berlin, Berlin, Germany. AD - Deutsches Rheumaforschungszentrum, Berlin, Germany. LA - eng PT - Clinical Trial, Phase II PT - Clinical Trial, Phase III PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - England TA - RMD Open JT - RMD open JID - 101662038 RN - ISP4442I3Y (baricitinib) SB - IM MH - Adult MH - Humans MH - *COVID-19 MH - COVID-19 Drug Treatment MH - *Venous Thromboembolism MH - *Lupus Erythematosus, Systemic/complications/diagnosis/drug therapy PMC - PMC10445377 OTO - NOTNLM OT - autoimmunity OT - immune system diseases OT - lupus erythematosus, systemic OT - therapeutics COIS- Competing interests: EM has been on speaker bureaus for, has been a consultant for, and or received grant/research support from: AbbVie, Amgen, Asahi Kasei Pharma, AstraZeneca, Biogen, Bristol Myers Squibb, Capella Therapeutics, Eli Lilly and Company, EMD Serono, Galapagos, Genentech, Gilead, GlaxoSmithKline, Janssen, Novartis, Sanofi, Servier, UCB Pharma, and Wolf Bio. JSS received grants to his institution from Abbvie, AstraZeneca, Lilly and Novatis and provided expert advice for, or had symposia speaking engagements with, AbbVie, Amgen, AstraZeneca, Astro, Biogen, Bristol Myers Squibb, Celgene, Celltrion, Chugai, Gilead, Janssen, Lilly, Merck Sharp & Dohme, Novartis-Sandoz, Pfizer, R-Pharma, Roche, Samsung, Sanofi, and UCB. MP has been a consultant for and received grant/research support from: Eli Lilly and Company. TD has been on speaker bureaus for, has been a consultant for, and/or received grant/research support from: AbbVie, BMS, Eli Lilly and Company, Janssen, Novartis, Roche, Samsung, Sanofi, and UCB Pharma; YT has been on speaker bureaus for, has been a consultant for, and/or received grant/research support from: AbbVie, Amgen, Astellas, AstraZeneca, AYUMI Pharmaceutical, Boehringer Ingelheim, Bristol Myers Squibb, Chugai Pharmaceutical, Daiichi Sankyo, Eisai, Eli Lilly and Company, Gilead Sciences, GlaxoSmithKline, Mitsubishi Tanabe, Sanofi, Taisho, and YL Biologics. YT has been on speaker bureaus for, has been a consultant for, and/or received grant/research support from: AbbVie, Amgen, Astellas, AstraZeneca, AYUMI Pharmaceutical, Boehringer Ingelheim, Bristol Myers Squibb, Chugai Pharmaceutical, Daiichi Sankyo, Eisai, Eli Lilly and Company, Gilead Sciences, GlaxoSmithKline, Mitsubishi Tanabe, Sanofi, Taisho, and YL Biologics. MS, CD, GM, IdlT and MI are employees and shareholders of Eli Lilly and Company. EDAT- 2023/08/22 00:42 MHDA- 2023/08/23 06:42 PMCR- 2023/08/21 CRDT- 2023/08/21 21:03 PHST- 2023/05/09 00:00 [received] PHST- 2023/08/05 00:00 [accepted] PHST- 2023/08/23 06:42 [medline] PHST- 2023/08/22 00:42 [pubmed] PHST- 2023/08/21 21:03 [entrez] PHST- 2023/08/21 00:00 [pmc-release] AID - rmdopen-2023-003302 [pii] AID - 10.1136/rmdopen-2023-003302 [doi] PST - ppublish SO - RMD Open. 2023 Aug;9(3):e003302. doi: 10.1136/rmdopen-2023-003302.