AI Article Synopsis

  • The study evaluated the effectiveness and safety of bimekizumab for treating psoriasis through a systematic review of randomized controlled trials (RCTs)!
  • A total of six studies with 1252 participants showed that bimekizumab significantly improved psoriasis symptoms (like PASI scores) compared to a placebo group, with various levels of improvement reported!
  • Results indicated that bimekizumab has a good safety profile, as there were no significant differences in adverse events between the bimekizumab and placebo groups!

Article Abstract

Aim: This study aimed to evaluate the efficacy and safety of bimekizumab for psoriasis.

Methods: The PubMed, Web of Science, Cochrane Library, and Embase databases were systematically searched until November 20, 2022, to identify randomized controlled trials (RCTs) reporting the efficacy and safety of bimekizumab. The identified studies were screened according to inclusion and exclusion criteria, and a meta-analysis was performed on the selected studies using the Stata (version 17.0) software to investigate the efficacy and safety of bimekizumab.

Results: Six studies involving 1252 participants were considered. Compared with the control group which received placebo, the bimekizumab group had a larger number of patients with improvement in Psoriasis Area and Severity Index (PASI) of at least 75% (PASI75) (RR: 20.54, 95%CI: 12.41-33.99;  = .000), at least 90% (PASI90) (RR:16.99, 95%CI: 7.09-40.68;  = .000) and 100%(PASI100) (RR:14.57; 95%CI: 5.26-40.35;  = .000) and a larger number with improvement in Investigator Global Assessment (IGA) response (RR:22.57; 95%CI: 12.74-39.98;  = .000). There was no obvious difference between the bimekizumab and placebo groups in treatment of emergent adverse events (TEAEs) (RR:1.17; 95%CI: 0.93-1.47; > .05) and serious TEAEs (RR: 0.67; 95%CI: 0.28-1.61; > .05).

Conclusions: Bimekizumab shows promising efficacy for the treatment of psoriasis with favorable safety records.

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Source
http://dx.doi.org/10.1080/09546634.2023.2199106DOI Listing

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