Certolizumab Pegol: A Review in Moderate to Severe Plaque Psoriasis
Version 2 2020-08-04, 03:51Version 2 2020-08-04, 03:51
Version 1 2020-03-29, 21:08Version 1 2020-03-29, 21:08
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posted on 2020-08-04, 03:51 authored by Arnold Lee, Lesley J Scott<div>Compliance with Ethical Standards</div><div><br></div><div><i>Funding:</i> The preparation of this review was not supported by any external funding.</div><div><br></div><div><i>Conflicts of interest:</i> Arnold Lee and Lesley Scott are salaried employees of Adis International Ltd/Springer Nature, are responsible for the article content and declare no relevant conflicts of interest.</div><div><br></div><div><p>Additional information about this Adis Drug Review can be
found <a href="https://www.springer.com/gp/adis/products-services/adis-journals-newsletters/adis-drug-reviews">here</a></p><br></div><div>Abstract</div><div><p>Certolizumab
pegol (Cimzia<sup>®</sup>) is a PEGylated, Fab'-only, recombinant humanized antibody
against TNF-α. Subcutaneous
certolizumab pegol is indicated for the treatment of various immune-mediated
inflammatory diseases (IMIDs), including moderate to severe plaque psoriasis. In
pivotal phase III trials in adults with moderate to severe plaque psoriasis, significantly
more patients receiving certolizumab pegol 200 mg or 400 mg once every 2 weeks than
placebo recipients achieved a ≥ 75% reduction in PASI score (PASI75 responder) and
a PGA score of clear/mostly clear with a ≥ 2 point improvement from baseline
(PGA0/1 responder) at week 12 (CIMPACT) or 16 (CIMPASI-1 and -2). In CIMPACT, certolizumab
pegol 400 mg once every 2 weeks was superior to etanercept (highest recommended
dosage) at 12 weeks, with certolizumab pegol 200 mg once every 2 weeks demonstrating
non-inferiority, but not superiority, to etanercept. The clinical benefits of
certolizumab pegol were maintained during the maintenance phase (to week 48)
and the open-label extension phase of these trials. Certolizumab pegol is
unique among the biologics, with the absence of an Fc fragment conferring
pharmacokinetic advantages; most notably, its minimal transfer across the placenta
or into breast milk. Certolizumab pegol was generally well tolerated and no new
safety signals were identified in these phase III trials, which complements its
established safety profile in other IMIDs. Certolizumab pegol is a useful
option for the treatment of moderate to severe plaque psoriasis and provides an
important treatment option for pregnant or breastfeeding patients, for whom
there are limited options available.</p>© Springer Nature Switzerland AG 2020<br></div>
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