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Certolizumab pegol.

Publication ,  Journal Article
Goel, N; Stephens, S
Published in: MAbs
2010

Certolizumab pegol (Cimzia(®)) is currently the only PEGylated anti-TNFα biologic approved for the treatment of rheumatoid arthritis and Crohn disease. The product, developed by UCB, is a humanized antigen-binding fragment (Fab') of a monoclonal antibody that has been conjugated to polyethylene glycol. Certolizumab pegol was approved as a treatment for rheumatoid arthritis in the EU, US and Canada in 2009, and as a treatment for Crohn disease in Switzerland in 2007 and the US in 2008. Certolizumab pegol is entering into an increasingly competitive marketplace, especially in rheumatoid arthritis, but clinical data demonstrate benefits across a range of clinical, radiographic and patient reported outcomes.

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Published In

MAbs

DOI

EISSN

1942-0870

Publication Date

2010

Volume

2

Issue

2

Start / End Page

137 / 147

Location

United States

Related Subject Headings

  • United States
  • Tumor Necrosis Factor-alpha
  • Polyethylene Glycols
  • Marketing
  • Immunotherapy
  • Immunology
  • Immunoglobulin Fab Fragments
  • Humans
  • European Union
  • Drug Approval
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Goel, N., & Stephens, S. (2010). Certolizumab pegol. MAbs, 2(2), 137–147. https://doi.org/10.4161/mabs.2.2.11271
Goel, Niti, and Sue Stephens. “Certolizumab pegol.MAbs 2, no. 2 (2010): 137–47. https://doi.org/10.4161/mabs.2.2.11271.
Goel N, Stephens S. Certolizumab pegol. MAbs. 2010;2(2):137–47.
Goel, Niti, and Sue Stephens. “Certolizumab pegol.MAbs, vol. 2, no. 2, 2010, pp. 137–47. Pubmed, doi:10.4161/mabs.2.2.11271.
Goel N, Stephens S. Certolizumab pegol. MAbs. 2010;2(2):137–147.

Published In

MAbs

DOI

EISSN

1942-0870

Publication Date

2010

Volume

2

Issue

2

Start / End Page

137 / 147

Location

United States

Related Subject Headings

  • United States
  • Tumor Necrosis Factor-alpha
  • Polyethylene Glycols
  • Marketing
  • Immunotherapy
  • Immunology
  • Immunoglobulin Fab Fragments
  • Humans
  • European Union
  • Drug Approval