Abstract | BACKGROUND: METHODS: We reviewed the results of the phase II clinical trials for the anti-IL-23 agents tildrakizumab and guselkumab, in order to assess the efficacy and safety profile of each agent. RESULTS: By week 16, the proportion of patients achieving Physician Global Assessment ( PGA) score of clear (0) or minimal (1) and Psoriasis Area and Severity Index (PASI 75) was above 70% among the most efficacious dosage of each agent (P < 0.001 compared to placebo for all agents). The safety profiles of the agents were similar, with the most frequently reported adverse events of nasopharyngitis, upper respiratory infections, cough, and headache. CONCLUSION: The anti-IL-23 agents demonstrated a rapid clinical improvement and favorable short-term safety profile. The results of the phase II trials support IL-23 as an essential target in psoriasis treatment.
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Authors | Kourosh Beroukhim, Melissa J Danesh, Catherine Nguyen, Annemieke Austin, John Koo, Ethan Levin |
Journal | Journal of drugs in dermatology : JDD
(J Drugs Dermatol)
Vol. 14
Issue 10
Pg. 1093-6
(Oct 2015)
ISSN: 1545-9616 [Print] United States |
PMID | 26461819
(Publication Type: Comparative Study, Journal Article, Review)
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Chemical References |
- Antibodies, Monoclonal
- Antibodies, Monoclonal, Humanized
- Dermatologic Agents
- Interleukin-23
- guselkumab
- tildrakizumab
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Topics |
- Antibodies, Monoclonal
(adverse effects, pharmacology, therapeutic use)
- Antibodies, Monoclonal, Humanized
- Clinical Trials, Phase II as Topic
- Dermatologic Agents
(adverse effects, pharmacology, therapeutic use)
- Humans
- Interleukin-23
(antagonists & inhibitors)
- Psoriasis
(drug therapy)
- Severity of Illness Index
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