FRI0161 Sustained Efficacy and Comparable Safety and Immunogenicity after Transition To SB5 (An Adalimumab Biosimilar) vs Continuation of The Adalimumab Reference Product in Patients with Rheumatoid Arthritis: Result of Phase III Study-Reference-Cited by-同舟云学术

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FRI0161 Sustained Efficacy and Comparable Safety and Immunogenicity after Transition To SB5 (An Adalimumab Biosimilar) vs Continuation of The Adalimumab Reference Product in Patients with Rheumatoid Arthritis: Result of Phase III Study

Published:2016-06 Issue:Suppl 2 Volume:75 Page:487.2-487
ISSN:0003-4967
Container-title:Annals of the Rheumatic Diseases
language:en
Short-container-title:Ann Rheum Dis

Author:

Weinblatt M.,Baranauskaite A.,Niebrzydowski J.,Dokoupilova E.,Zielinska A.,Sitek-Ziolkowska K.,Jaworski J.,Racewicz A.,Pileckyte M.,Jedrychowicz-Rosiak K.,Zhdan V.,Cheong S.Y.,Ghil J.

Publisher

BMJ

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,Immunology and Allergy,Rheumatology

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Biogen and Samsung Bioepis Announce European Launch of IMRALDI™ (adalimumab), Solidifying Leadership in European Anti-TNF Market;Rheumatology;2018-11-30

2. Biologics for treating axial spondyloarthritis;Expert Opinion on Biological Therapy;2018-05-07

3. Biosimilars: considerations for clinical practice;Considerations in Medicine;2017-10-01

4. Switching Between Reference Biologics and Biosimilars for the Treatment of Rheumatology, Gastroenterology, and Dermatology Inflammatory Conditions: Considerations for the Clinician;Current Rheumatology Reports;2017-06

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