Literature DB >> 24447441

Certolizumab for rheumatoid arthritis.

T E Markatseli1, C Papagoras, A Nikoli, P V Voulgari, A A Drosos.   

Abstract

This is a review of the pharmacology of certolizumab pegol and its efficacy and safety in the treatment of patients with rheumatoid arthritis refractory to synthetic disease-modifying anti-rheumatic drugs (DMARDs). Certolizumab is a new anti-TNF-α biologic agent injected subcutaneously with an innovative molecular structure and unique pharmacodynamic and pharmacokinetic properties. Data from controlled clinical trials indicate that the drug is effective in reducing disease activity and disability. It also inhibits radiographic progression. Certolizumab administration has an acceptable safety profile. The clinical data available suggest that the nature of adverse events is generally comparable to that of other TNF-α blockers. Given its rapid onset of action certolizumab presents an attractive alternative therapeutic option for patients with moderate to severe RA refractory to DMARDs.

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Year:  2014        PMID: 24447441

Source DB:  PubMed          Journal:  Clin Exp Rheumatol        ISSN: 0392-856X            Impact factor:   4.473


  3 in total

Review 1.  Immunology proves a great success for treating systemic autoimmune diseases - a perspective on immunopharmacology: IUPHAR Review 23.

Authors:  Masaru Ishii
Journal:  Br J Pharmacol       Date:  2017-04-24       Impact factor: 8.739

2.  Matrix metalloproteinase-3 and the 7-joint ultrasound score in the assessment of disease activity and therapeutic efficacy in patients with moderate to severe rheumatoid arthritis.

Authors:  Ling Zhou; Geng Wang; Xin Liu; Jing Song; Ling Chen; Huji Xu
Journal:  Arthritis Res Ther       Date:  2017-11-15       Impact factor: 5.156

3.  The polymethoxy flavonoid sudachitin suppresses inflammatory bone destruction by directly inhibiting osteoclastogenesis due to reduced ROS production and MAPK activation in osteoclast precursors.

Authors:  Yoko Ohyama; Junta Ito; Victor J Kitano; Jun Shimada; Yoshiyuki Hakeda
Journal:  PLoS One       Date:  2018-01-17       Impact factor: 3.240

  3 in total

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