Utilization and Treatment Costs of Tumor Necrosis Factor Inhibitors After the Introduction of Biosimilar Infliximab in the United States
- PMID: 31943866
- DOI: 10.1002/art.41201
Utilization and Treatment Costs of Tumor Necrosis Factor Inhibitors After the Introduction of Biosimilar Infliximab in the United States
Comment in
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Failure to Launch: Biosimilar Sales Continue to Fall Flat in the United States.Arthritis Rheumatol. 2020 Jun;72(6):870-873. doi: 10.1002/art.41203. Epub 2020 Apr 23. Arthritis Rheumatol. 2020. PMID: 31922346 Free PMC article. No abstract available.
References
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- Sarpatwari A, Barenie R, Curfman G, Darrow JJ, Kesselheim AS. The US biosimilar market: stunted growth and possible reforms. Clin Pharmacol Ther 2019;105:92-100.
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- Glintborg B, Sorensen IJ, Loft AG, Lindegaard H, Linauskas A, Hendricks O, et al, on behalf of all departments of rheumatology in Denmark. A nationwide non-medical switch from originator infliximab to biosimilar CT-P13 in 802 patients with inflammatory arthritis: 1-year clinical outcomes from the DANBIO registry. Ann Rheum Dis 2017;76:1426-31.
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- Yazdany J, Dudley RA, Lin GA, Chen R, Tseng CW. Out-of-pocket costs for infliximab and its biosimilar for rheumatoid arthritis under Medicare Part D. JAMA 2018;320:931-3.
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