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SB4 in the Era of Biosimilars: Clinical Data and Real-World Experience.

作者信息

Law Shing T, Taylor Peter C

机构信息

Botnar Research Centre, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom.

出版信息

Mediterr J Rheumatol. 2019 May 31;30(Suppl 1):59-62. doi: 10.31138/mjr.30.1.59. eCollection 2019 Jun.

Abstract

A biosimilar is a biological medicinal product that is highly similar to an already authorized original biological medicinal product. The introduction of biosimilars may allow for a reduction in health care costs, due to discount pricing. Current clinical studies and real-world data suggest that the biosimilar SB4 is equivalent to etanercept with respect to efficacy and safety. Additional real-world safety data for SB4 via pharmacovigilance studies are needed to draw conclusions regarding the risks of rare adverse events such as serious infections and malignancy. Clinical trial design of biosimilars should be standardised to improve consistency, increase confidence and facilitate interpretation of data. Where there are health economic advantages of switching from originator to biosimilar, patients should be appropriately informed, and, ideally, in order to minimise nocebo responses and maximise benefit, switching should be undertaken by shared decision-making between the physician and patient on a case-by-case basis.

摘要

相似文献

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SB4 in the Era of Biosimilars: Clinical Data and Real-World Experience.
Mediterr J Rheumatol. 2019 May 31;30(Suppl 1):59-62. doi: 10.31138/mjr.30.1.59. eCollection 2019 Jun.

本文引用的文献

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Clinical trials of biosimilars should become more similar.生物类似药的临床试验应更具相似性。
Ann Rheum Dis. 2017 Jan;76(1):4-6. doi: 10.1136/annrheumdis-2015-208113. Epub 2016 Aug 25.
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The changing landscape of biosimilars in rheumatology.风湿病领域生物类似药不断变化的局面。
Ann Rheum Dis. 2016 Jun;75(6):974-82. doi: 10.1136/annrheumdis-2016-209166. Epub 2016 Mar 8.

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