Efficacy and safety data based on historical or pre-existing conditions at baseline for patients with active rheumatoid arthritis who were treated with baricitinib

Bernard Combe, Alejandro Balsa, Piercarlo Sarzi-Puttini, Hans-Peter Tony, Inmaculada de la Torre, Veronica Rogai, Frederick Durand, Sarah Witt, Jinglin Zhong, Maxime Dougados, Bernard Combe, Alejandro Balsa, Piercarlo Sarzi-Puttini, Hans-Peter Tony, Inmaculada de la Torre, Veronica Rogai, Frederick Durand, Sarah Witt, Jinglin Zhong, Maxime Dougados

No abstract available

Keywords: DMARDs (synthetic); rheumatoid arthritis; treatment.

Conflict of interest statement

Competing interests: BC reports grants and personal fees from Merck and Pfizer, and personal fees from AbbVie, BMS, Janssen, Eli Lilly, Roche Chugai, Sanofi and UCB, outside the submitted work. AB reports grants and personal fees from Eli Lilly, during the conduct of the study, and grants from Pfizer, AbbVie, MSD and BMS, grants and personal fees from Novartis and Nordic, and personal fees from UCB, Celltrion, Kern Pharma, Sanofi and Sandoz, outside the submitted work. H-PT reports personal fees from AbbVie, Chugai, Janssen Cilag, Eli Lilly, Novartis, Roche, Sandoz Hexal and Sanofi Aventis, outside the submitted work. MD reports grants and personal fees from Eli Lilly, Pfizer, AbbVie and UCB, during the conduct of the study. VR is a minor shareholder of Eli Lilly and Company. PSP, JZ, IdlT, FD and SW report no conflicts of interest.

References

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    1. Keystone EC, Taylor PC, Drescher E, et al. . Safety and efficacy of baricitinib at 24 weeks in patients with rheumatoid arthritis who have had an inadequate response to methotrexate. Ann Rheum Dis 2015;74:333–40. 10.1136/annrheumdis-2014-206478
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    1. INCB028050 compared to background therapy in patients with active rheumatoid arthritis (RA) with inadequate response to disease modifying anti-rheumatic drugs, 2009. Available: [Accessed 18 Mar 2018].
    1. Dougados M, van der Heijde D, Chen Y-C, et al. . Baricitinib in patients with inadequate response or intolerance to conventional synthetic DMARDs: results from the RA-BUILD study. Ann Rheum Dis 2017;76:88–95. 10.1136/annrheumdis-2016-210094
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Source: PubMed

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