Safety of Ixekizumab Treatment for up to 5 Years in Adult Patients with Moderate-to-Severe Psoriasis: Results from Greater Than 17,000 Patient-Years of Exposure.

Adverse events Etanercept IL-17 Integrated analysis Ixekizumab Psoriasis Safety

Journal

Dermatology and therapy
ISSN: 2193-8210
Titre abrégé: Dermatol Ther (Heidelb)
Pays: Switzerland
ID NLM: 101590450

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 08 08 2019
pubmed: 22 11 2019
medline: 22 11 2019
entrez: 22 11 2019
Statut: ppublish

Résumé

Long-term safety data are critical for evaluating therapies for psoriasis. Ixekizumab has demonstrated efficacy and is well tolerated for the treatment of moderate-to-severe plaque psoriasis. We examined the safety and tolerability of up to 5 years of ixekizumab therapy in patients with psoriasis. Integrated safety data were analyzed from 13 ixekizumab clinical studies. Rates of treatment-emergent adverse events (TEAEs), serious AEs (SAEs) and AEs of special interest were analyzed for the 12-week induction period in the combined pivotal studies, and for all pooled studies by year(s) of therapy and overall, reported as exposure-adjusted incidence rates (IRs) per 100 patient-years (p-y) and/or frequencies. Total ixekizumab exposure was 17,003.4 p-y (N = 5898); 2749 patients had ≥ 4 years of exposure. When compared across years of exposure, rates for AEs remained largely stable or declined, including TEAEs leading to discontinuation (3.8/100 p-y in year 1, declining to 2.0/100 p-y in year 5); SAEs (range 6.2-7.0/100 p-y); serious infections (range 1.3-1.7/100 p-y); nonmelanoma skin cancer (ranging from 0.5/100 p-y in year 1 to 0.2/100 p-y in years 4-5); other malignancies (range 0.4-0.6/100 p-y); inflammatory bowel disease including ulcerative colitis and Crohn's disease (IR 0.2/100 p-y); and major adverse cardiovascular events (MACE) (range 0.3-0.7/100 p-y). Candidiasis was reported in 327 patients (IR 1.9/100 p-y), with the majority identified as mucocutaneous. The rate of injection site reactions was 15.5/100 p-y during year 1 and 2.0-2.3/100 p-y by years 3-5. The decrease in rates of TEAEs and the stable rates of SAEs, other malignancies and MACE during up to 5 years of ixekizumab dosing are consistent with previous reports describing a favorable safety profile of ixekizumab following shorter durations of exposure. Eli Lilly and Company.

Identifiants

pubmed: 31749092
doi: 10.1007/s13555-019-00340-3
pii: 10.1007/s13555-019-00340-3
pmc: PMC6994584
doi:

Types de publication

Journal Article

Langues

eng

Pagination

133-150

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Auteurs

April Armstrong (A)

Department of Clinical Research, Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA. armstrongpublication@gmail.com.

Carle Paul (C)

Dermatology Department, Toulouse University Hospital (CHU), Paul Sabatier University, Toulouse, France.

Luis Puig (L)

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

Wolf Henning Boehncke (WH)

Division of Dermatology and Venereology, Geneva University Hospitals, Geneva, Switzerland.
Department of Pathology and Immunology, University of Geneva, Geneva, Switzerland.

Michael Freeman (M)

The Skin Centre, Benowa, QLD, Australia.

Hideshi Torii (H)

Division of Dermatology, Tokyo Yamate Medical Center, Tokyo, Japan.

Kim Papp (K)

K Papp Clinical Research and Probity Medical Research, Waterloo, ON, Canada.

Christopher E M Griffiths (CEM)

Dermatology Centre, Salford Royal Hospital, University of Manchester, NIHR Manchester Biomedical Research Centre, Manchester, UK.

Andrew Blauvelt (A)

Oregon Medical Research Center, Portland, OR, USA.

Kristian Reich (K)

Center for Translational Research in Inflammatory Skin Diseases, Institute for Health Services Research in Dermatology and Nursing, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Skinflammation® Center, Hamburg, Germany.

Melinda Gooderham (M)

Centre for Dermatology and Probity Medical Research, Peterborough, ON, Canada.

Tadashi Terui (T)

Department of Dermatology, Nihon University School of Medicine, Tokyo, Japan.

Lisa Renda (L)

Eli Lilly and Company, Indianapolis, IN, USA.

Noah Agada (N)

Eli Lilly and Company, Indianapolis, IN, USA.

Wen Xu (W)

Eli Lilly and Company, Indianapolis, IN, USA.

Gaia Gallo (G)

Eli Lilly and Company, Indianapolis, IN, USA.

Mark G Lebwohl (MG)

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

Classifications MeSH