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Population pharmacokinetic and exposure–response analysis of apremilast in Japanese subjects with moderate to severe psoriasis
Apremilast is an orally available phosphodiesterase 4 inhibitor used for the treatment of moderate to severe psoriasis. The aims of this analysis were to develop a population pharmacokinetic (PPK) model of apremilast based on observed data from phase 1 studies combined with clinical trial data from...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290614/ https://www.ncbi.nlm.nih.gov/pubmed/34396569 http://dx.doi.org/10.1111/1346-8138.16068 |
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author | Okubo, Yukari Ohtsuki, Mamitaro Komine, Mayumi Imafuku, Shinichi Kassir, Nastya Petric, Rosemary Nemoto, Osamu |
author_facet | Okubo, Yukari Ohtsuki, Mamitaro Komine, Mayumi Imafuku, Shinichi Kassir, Nastya Petric, Rosemary Nemoto, Osamu |
author_sort | Okubo, Yukari |
collection | PubMed |
description | Apremilast is an orally available phosphodiesterase 4 inhibitor used for the treatment of moderate to severe psoriasis. The aims of this analysis were to develop a population pharmacokinetic (PPK) model of apremilast based on observed data from phase 1 studies combined with clinical trial data from subjects with moderate to severe psoriasis, and to develop exposure–response (E‐R) models to determine whether Japanese subjects with moderate to severe psoriasis achieve response to apremilast treatment similar to that observed in non‐Japanese, predominantly Caucasian subjects with moderate to severe psoriasis. The PPK model demonstrated that apremilast plasma concentrations and overall apparent clearance rate were comparable between the Japanese and Caucasian subgroups. The E‐R analyses of ≥75% or ≥50% improvement from baseline in Psoriasis Area and Severity Index score and achievement of static Physician Global Assessment score of 0 (clear) or 1 (almost clear) at week 16 indicated that apremilast treatment in Japanese subjects approached the maximal effect with response rates comparable to those in predominantly Caucasian subjects. Overall, the analyses confirm that the approved apremilast 30 mg b.i.d. dose is appropriate for Japanese subjects with moderate to severe psoriasis, with an efficacy profile similar to that previously observed in Caucasian subjects. |
format | Online Article Text |
id | pubmed-9290614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92906142022-07-20 Population pharmacokinetic and exposure–response analysis of apremilast in Japanese subjects with moderate to severe psoriasis Okubo, Yukari Ohtsuki, Mamitaro Komine, Mayumi Imafuku, Shinichi Kassir, Nastya Petric, Rosemary Nemoto, Osamu J Dermatol Original Articles Apremilast is an orally available phosphodiesterase 4 inhibitor used for the treatment of moderate to severe psoriasis. The aims of this analysis were to develop a population pharmacokinetic (PPK) model of apremilast based on observed data from phase 1 studies combined with clinical trial data from subjects with moderate to severe psoriasis, and to develop exposure–response (E‐R) models to determine whether Japanese subjects with moderate to severe psoriasis achieve response to apremilast treatment similar to that observed in non‐Japanese, predominantly Caucasian subjects with moderate to severe psoriasis. The PPK model demonstrated that apremilast plasma concentrations and overall apparent clearance rate were comparable between the Japanese and Caucasian subgroups. The E‐R analyses of ≥75% or ≥50% improvement from baseline in Psoriasis Area and Severity Index score and achievement of static Physician Global Assessment score of 0 (clear) or 1 (almost clear) at week 16 indicated that apremilast treatment in Japanese subjects approached the maximal effect with response rates comparable to those in predominantly Caucasian subjects. Overall, the analyses confirm that the approved apremilast 30 mg b.i.d. dose is appropriate for Japanese subjects with moderate to severe psoriasis, with an efficacy profile similar to that previously observed in Caucasian subjects. John Wiley and Sons Inc. 2021-08-15 2021-11 /pmc/articles/PMC9290614/ /pubmed/34396569 http://dx.doi.org/10.1111/1346-8138.16068 Text en © 2021 The Authors. The Journal of Dermatology published by John Wiley & Sons Australia, Ltd on behalf of Japanese Dermatological Association https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Okubo, Yukari Ohtsuki, Mamitaro Komine, Mayumi Imafuku, Shinichi Kassir, Nastya Petric, Rosemary Nemoto, Osamu Population pharmacokinetic and exposure–response analysis of apremilast in Japanese subjects with moderate to severe psoriasis |
title | Population pharmacokinetic and exposure–response analysis of apremilast in Japanese subjects with moderate to severe psoriasis |
title_full | Population pharmacokinetic and exposure–response analysis of apremilast in Japanese subjects with moderate to severe psoriasis |
title_fullStr | Population pharmacokinetic and exposure–response analysis of apremilast in Japanese subjects with moderate to severe psoriasis |
title_full_unstemmed | Population pharmacokinetic and exposure–response analysis of apremilast in Japanese subjects with moderate to severe psoriasis |
title_short | Population pharmacokinetic and exposure–response analysis of apremilast in Japanese subjects with moderate to severe psoriasis |
title_sort | population pharmacokinetic and exposure–response analysis of apremilast in japanese subjects with moderate to severe psoriasis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290614/ https://www.ncbi.nlm.nih.gov/pubmed/34396569 http://dx.doi.org/10.1111/1346-8138.16068 |
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