Real-world effectiveness and safety of bimekizumab for hidradenitis suppurativa: An ambispective observational study

Australas J Dermatol. 2024 Nov;65(7):e198-e202. doi: 10.1111/ajd.14339. Epub 2024 Jun 19.

Abstract

In this original research, we present the results in terms of effectiveness and safety of bimekizumab for hidradenitis suppurativa in real clinical practice. Results indicated significant improvement in all activity scores and patient-reported outcomes at week 16, including a notable decrease in mean IHS4 from 27.1 to 15.6 (p < 0.001), HS-PGA from 5.1 to 3.2 (p < 0.001), VAS pain from 8.3 to 4.7 (p < 0.001) and DLQI from 21.6 to 12.6 (p < 0.001). Bimekizumab, administered every 2 or 4 weeks, was well-tolerated with no discontinuations and no new safety concerns identified. These findings corroborate the drug's effectiveness and favourable safety profile observed in phase 3 clinical trials, supporting its use in real-world clinical practice for treating HS.

Keywords: bimekizumab; biologic therapy; effectiveness; hidradenitis suppurativa; safety.

Publication types

  • Observational Study

MeSH terms

  • Adult
  • Antibodies, Monoclonal, Humanized / adverse effects
  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Dermatologic Agents / adverse effects
  • Dermatologic Agents / therapeutic use
  • Female
  • Hidradenitis Suppurativa* / drug therapy
  • Humans
  • Male
  • Middle Aged
  • Patient Reported Outcome Measures
  • Severity of Illness Index
  • Treatment Outcome

Substances

  • bimekizumab
  • Antibodies, Monoclonal, Humanized
  • Dermatologic Agents