Drug safety evaluation of tildrakizumab for psoriasis: a review of the current knowledge.

Abstract

INTRODUCTION:

Psoriasis is a chronic inflammatory skin disease that may have an important negative impact on a patient's quality of life. Biological agents deeply changed the management of its moderate-to-severe forms. Interleukin-23 inhibitors represent the latest biologics class approved for the treatment of moderate-to-severe psoriasis. In particular, tildrakizumab, the latest available anti-interleukin-23 on the Italian market, is a humanized monoclonal antibody specifically targeting the p19 subunit of IL-23.

AREAS COVERED:

The objective of this review is to evaluate the safety profile of tildrakizumab in moderate-to-severe psoriasis patients. A literature review included articles until July 2022.

EXPERT OPINION:

Our analysis showed tildrakizumab as a generally safe option for the treatment of psoriasis, with most of the reported adverse events being classified as mild or moderate, and rarely requiring treatment discontinuation. Furthermore, in line with other interleukin-23 inhibitor, no concerns have been raised for tildrakizumab in regard to inflammatory bowel diseases, which represent a significant comorbidity to investigate before starting other biologics (IL-17 inhibitors). However, more real-life long-term data are needed to confirm trial results to further confirm tildrakizumab as a generally safe treatment option for psoriasis.

• Authors: Angelo Ruggiero, Elisa Camela, Luca Potestio, Gabriella Fabbrocini, Matteo Megna
• Journal: Expert opinion on drug safety (Expert Opin Drug Saf) Vol. 21 Issue 12 Pg. 1445-1451 (Dec 2022) ISSN: 1744-764X [Electronic] England
• PMID: 36527300 (Publication Type: Review, Journal Article)

Chemical References

• tildrakizumab
• Antibodies, Monoclonal

Topics

• Humans
• Antibodies, Monoclonal (adverse effects)
• Quality of Life
• Treatment Outcome
• Psoriasis
• Chronic Disease