Title : Certolizumab pegol: a review of its use in patients with axial spondyloarthritis or psoriatic arthritis.

Pub. Date : 2014 Jun

PMID : 24919863






4 Functional Relationships(s)
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1 In the EU, subcutaneous certolizumab pegol is indicated for the treatment of adults with severe active axial spondyloarthritis (axSpA), comprising ankylosing spondylitis (AS) and non-radiographic axSpA (nr-axSpA), and for adults with active psoriatic arthritis (PsA). Certolizumab Pegol aminopeptidase puromycin sensitive Homo sapiens
2 In two ongoing, well-designed studies, data at 12 and 24 weeks showed that treatment with certolizumab pegol (200 mg every 2 weeks or 400 mg every 4 weeks) was effective in improving the clinical signs and symptoms of disease, health-related quality of life and productivity in patients with axSpA (the RAPID-axSpA study) or PsA (the RAPID-PsA study), with the improvements maintained during longer-term (48 weeks) treatment. Certolizumab Pegol aminopeptidase puromycin sensitive Homo sapiens
3 In two ongoing, well-designed studies, data at 12 and 24 weeks showed that treatment with certolizumab pegol (200 mg every 2 weeks or 400 mg every 4 weeks) was effective in improving the clinical signs and symptoms of disease, health-related quality of life and productivity in patients with axSpA (the RAPID-axSpA study) or PsA (the RAPID-PsA study), with the improvements maintained during longer-term (48 weeks) treatment. Certolizumab Pegol aminopeptidase puromycin sensitive Homo sapiens
4 In addition, 12 weeks" treatment with certolizumab pegol reduced inflammation in the sacroiliac joints and spine in patients with axSpA and 24 weeks" treatment with the agent slowed radiographic disease progression in patients with PsA. Certolizumab Pegol aminopeptidase puromycin sensitive Homo sapiens