Treatment-emergent candida infections in patients with psoriasis, psoriatic arthritis, and axial spondyloarthritis treated with Ixekizumab: an integrated safety analysis of 25 clinical studies.

Axial spondyloarthritis Candida Infections Ixekizumab Psoriasis integrated long-term safety psoriatic arthritis

Journal

Expert opinion on drug safety
ISSN: 1744-764X
Titre abrégé: Expert Opin Drug Saf
Pays: England
ID NLM: 101163027

Informations de publication

Date de publication:
05 Sep 2024
Historique:
medline: 5 9 2024
pubmed: 5 9 2024
entrez: 5 9 2024
Statut: aheadofprint

Résumé

This safety analysis investigates treatment-emergent mucosal/cutaneous Candida infections in patients treated with ixekizumab (IXE), an anti-interleukin-17A monoclonal antibody, across the approved indications: psoriasis (PsO), psoriatic arthritis (PsA), and axial spondyloarthritis (axSpA). Safety data were pooled from 25 clinical studies. Incidence rates (IRs) are expressed as per 100 patient-years (PY), using the entire duration of exposure. Candida infections had an IR of 1.9 per 100 PY in patients with PsO ( This integrated safety analysis shows that the risk of developing Candida infections is low with IXE, and the severity is mild-to-moderate in most instances across the approved IXE indications. A comprehensive list of the clinical trials and their registration numbers is reported in Table S1 of the supplemental material. Ixekizumab(IXE) is a drug approved for the treatment of psoriasis, psoriatic arthritis,and axial spondyloarthritis. IXE belongs to the class of molecules that block aprotein called interleukin-17A. Since interleukin-17A is involved in the defenseagainst fungi, the clinical use of this class of drug has the potential to increasethe risk of developing fungal infections, such as Candida infections.Therefore, researcherscollected safety data from 25 clinical studies comprising 9225 adult patientstreated with IXE: 6892 with psoriasis, 1401 with psoriatic arthritis, and 932with axial spondyloarthritis. Researchers looked at the rate of new cases of Candidainfections, the so-called incidence rate, and found that 1.9 per 100patient-years experienced at least 1 Candida infection in the psoriasis group, 2.0per 100 patient-years in the psoriatic arthritis group, and 1.2 per 100patient-years in the axial spondyloarthritis group.Acrossindications, the majority of Candida infections (

Sections du résumé

BACKGROUND UNASSIGNED
This safety analysis investigates treatment-emergent mucosal/cutaneous Candida infections in patients treated with ixekizumab (IXE), an anti-interleukin-17A monoclonal antibody, across the approved indications: psoriasis (PsO), psoriatic arthritis (PsA), and axial spondyloarthritis (axSpA).
RESEARCH DESIGN AND METHODS UNASSIGNED
Safety data were pooled from 25 clinical studies. Incidence rates (IRs) are expressed as per 100 patient-years (PY), using the entire duration of exposure.
RESULTS UNASSIGNED
Candida infections had an IR of 1.9 per 100 PY in patients with PsO (
CONCLUSIONS UNASSIGNED
This integrated safety analysis shows that the risk of developing Candida infections is low with IXE, and the severity is mild-to-moderate in most instances across the approved IXE indications.
TRIAL REGISTRATION UNASSIGNED
A comprehensive list of the clinical trials and their registration numbers is reported in Table S1 of the supplemental material.
Ixekizumab(IXE) is a drug approved for the treatment of psoriasis, psoriatic arthritis,and axial spondyloarthritis. IXE belongs to the class of molecules that block aprotein called interleukin-17A. Since interleukin-17A is involved in the defenseagainst fungi, the clinical use of this class of drug has the potential to increasethe risk of developing fungal infections, such as Candida infections.Therefore, researcherscollected safety data from 25 clinical studies comprising 9225 adult patientstreated with IXE: 6892 with psoriasis, 1401 with psoriatic arthritis, and 932with axial spondyloarthritis. Researchers looked at the rate of new cases of Candidainfections, the so-called incidence rate, and found that 1.9 per 100patient-years experienced at least 1 Candida infection in the psoriasis group, 2.0per 100 patient-years in the psoriatic arthritis group, and 1.2 per 100patient-years in the axial spondyloarthritis group.Acrossindications, the majority of Candida infections (

Autres résumés

Type: plain-language-summary (eng)
Ixekizumab(IXE) is a drug approved for the treatment of psoriasis, psoriatic arthritis,and axial spondyloarthritis. IXE belongs to the class of molecules that block aprotein called interleukin-17A. Since interleukin-17A is involved in the defenseagainst fungi, the clinical use of this class of drug has the potential to increasethe risk of developing fungal infections, such as Candida infections.Therefore, researcherscollected safety data from 25 clinical studies comprising 9225 adult patientstreated with IXE: 6892 with psoriasis, 1401 with psoriatic arthritis, and 932with axial spondyloarthritis. Researchers looked at the rate of new cases of Candidainfections, the so-called incidence rate, and found that 1.9 per 100patient-years experienced at least 1 Candida infection in the psoriasis group, 2.0per 100 patient-years in the psoriatic arthritis group, and 1.2 per 100patient-years in the axial spondyloarthritis group.Acrossindications, the majority of Candida infections (

Identifiants

pubmed: 39234767
doi: 10.1080/14740338.2024.2399092
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Sergio Schwartzman (S)

Hospital for Special Surgery, New York, USA.

Luis Puig (L)

Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Arnon D Cohen (AD)

Clalit Health Services, Tel Aviv, Israel.

Saakshi Khattri (S)

Icahn School of Medicine at Mount Sinai, New York, USA.

Christian Jossart (C)

Eli Lilly and Company, Indianapolis, USA.

Carlos Diaz (C)

Eli Lilly and Company, Indianapolis, USA.

Alyssa Garrelts (A)

Eli Lilly and Company, Indianapolis, USA.

Marcus Ngantcha (M)

Eli Lilly and Company, Indianapolis, USA.

Nadezhda Eberhart (N)

Eli Lilly and Company, Indianapolis, USA.

Areti Eleftheriadi (A)

Eli Lilly and Company, Indianapolis, USA.

Nithi Tangsirisap (N)

Eli Lilly and Company, Indianapolis, USA.

Christopher Schuster (C)

Eli Lilly and Company, Indianapolis, USA.
Medical University of Vienna, Vienna, Austria.

Alice B Gottlieb (AB)

Icahn School of Medicine at Mount Sinai, New York, USA.

Classifications MeSH