Population Pharmacokinetic-Pharmacodynamic (popPK/PD) Relationship of Orismilast, A Potent and Selective PDE4B/D Inhibitor, in Atopic Dermatitis.

IF 3.5 3区 医学 Q1 DERMATOLOGY
Dermatology and Therapy Pub Date : 2025-04-01 Epub Date: 2025-03-05 DOI:10.1007/s13555-025-01371-9
Richard B Warren, Anne Weiss, Jakob Felding, Morten O A Sommer
{"title":"Population Pharmacokinetic-Pharmacodynamic (popPK/PD) Relationship of Orismilast, A Potent and Selective PDE4B/D Inhibitor, in Atopic Dermatitis.","authors":"Richard B Warren, Anne Weiss, Jakob Felding, Morten O A Sommer","doi":"10.1007/s13555-025-01371-9","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Orismilast is a novel oral selective inhibitor of phosphodiesterase 4B and 4D subtypes (PDE4B/D) in clinical development for treatment of atopic dermatitis (AD) and other inflammatory skin conditions. Herein, we describe a pharmacokinetic/pharmacodynamic (PK/PD) analysis comparing predicted exposure data of orismilast and apremilast in AD patients and place these data in the context of their IL-13 secretion data generated in a human whole-blood assay.</p><p><strong>Methods: </strong>A PK/PD assessment of orismilast and apremilast in AD was performed. In a human whole blood assay, the levels needed to inhibit IL-13 production were measured for orismilast and apremilast head-to-head. These data were then contextualized with simulated exposure of clinically relevant doses of the two drugs.</p><p><strong>Results: </strong>The analysis shows that orismilast has potential to significantly inhibit IL-13 production at all three clinical doses trialed in AD (20 mg bid, 30 mg bid, and 40 mg bid) as the drug has a predicted C<sub>average</sub> plasma concentration exceeding the IL-13 IC<sub>90</sub> value of the human whole-blood assay and a predicted C<sub>min</sub> above the IL-13 IC<sub>50</sub> value. Apremilast, in contrast, is predicted to reach C<sub>average</sub> plasma concentrations below the IL-13 IC<sub>50</sub> value for both doses (30 mg bid and 40 mg bid) and only exceeding the IL-13 IC<sub>50</sub> value at peak concentrations for the highest dose.</p><p><strong>Conclusion: </strong>The outcome of the analysis supports the observed clinical effect of orismilast in patients with AD and could explain the lack of efficacy of apremilast in the same indication.</p>","PeriodicalId":11186,"journal":{"name":"Dermatology and Therapy","volume":" ","pages":"831-839"},"PeriodicalIF":3.5000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11971100/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dermatology and Therapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s13555-025-01371-9","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/5 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"DERMATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Orismilast is a novel oral selective inhibitor of phosphodiesterase 4B and 4D subtypes (PDE4B/D) in clinical development for treatment of atopic dermatitis (AD) and other inflammatory skin conditions. Herein, we describe a pharmacokinetic/pharmacodynamic (PK/PD) analysis comparing predicted exposure data of orismilast and apremilast in AD patients and place these data in the context of their IL-13 secretion data generated in a human whole-blood assay.

Methods: A PK/PD assessment of orismilast and apremilast in AD was performed. In a human whole blood assay, the levels needed to inhibit IL-13 production were measured for orismilast and apremilast head-to-head. These data were then contextualized with simulated exposure of clinically relevant doses of the two drugs.

Results: The analysis shows that orismilast has potential to significantly inhibit IL-13 production at all three clinical doses trialed in AD (20 mg bid, 30 mg bid, and 40 mg bid) as the drug has a predicted Caverage plasma concentration exceeding the IL-13 IC90 value of the human whole-blood assay and a predicted Cmin above the IL-13 IC50 value. Apremilast, in contrast, is predicted to reach Caverage plasma concentrations below the IL-13 IC50 value for both doses (30 mg bid and 40 mg bid) and only exceeding the IL-13 IC50 value at peak concentrations for the highest dose.

Conclusion: The outcome of the analysis supports the observed clinical effect of orismilast in patients with AD and could explain the lack of efficacy of apremilast in the same indication.

Orismilast是一种有效的选择性PDE4B/D抑制剂,在特应性皮炎中的群体药代动力学-药效学(popPK/PD)关系。
Orismilast是一种新型口服选择性磷酸二酯酶4B和4D亚型(PDE4B/D)抑制剂,临床开发用于治疗特应性皮炎(AD)和其他炎症性皮肤疾病。在此,我们描述了一种药代动力学/药效学(PK/PD)分析,比较了奥瑞米司特和阿普雷米司特在AD患者中的预测暴露数据,并将这些数据与人类全血测定中产生的IL-13分泌数据结合起来。方法:对奥司米司特和阿普雷米司特在AD患者的PK/PD进行评价。在人全血试验中,测定了orismilast和apremilast头对头抑制IL-13产生所需的水平。然后将这些数据与两种药物临床相关剂量的模拟暴露联系起来。结果:分析显示orismilast在AD临床试验的所有三种剂量(20mg bid, 30mg bid和40mg bid)下具有显著抑制IL-13产生的潜力,因为该药物的预测平均血浆浓度超过人全血测定的IL-13 IC90值,预测Cmin高于IL-13 IC50值。相比之下,阿普雷米司特的平均血浆浓度在两种剂量(30mg bid和40mg bid)下均低于IL-13 IC50值,只有在最高剂量时达到峰值浓度时才超过IL-13 IC50值。结论:本分析结果支持奥瑞米司特治疗AD患者的临床疗效观察,可以解释阿普米司特在同一适应症中疗效不足的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Dermatology and Therapy
Dermatology and Therapy Medicine-Dermatology
CiteScore
6.00
自引率
8.80%
发文量
187
审稿时长
6 weeks
期刊介绍: Dermatology and Therapy is an international, open access, peer-reviewed, rapid publication journal (peer review in 2 weeks, published 3–4 weeks from acceptance). The journal is dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of dermatological therapies. Studies relating to diagnosis, pharmacoeconomics, public health and epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to all clinical aspects of dermatology, such as skin pharmacology; skin development and aging; prevention, diagnosis, and management of skin disorders and melanomas; research into dermal structures and pathology; and all areas of aesthetic dermatology, including skin maintenance, dermatological surgery, and lasers. The journal is of interest to a broad audience of pharmaceutical and healthcare professionals and publishes original research, reviews, case reports/case series, trial protocols, and short communications. Dermatology and Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an International and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of quality research, which may be considered of insufficient interest by other journals. The journal appeals to a global audience and receives submissions from all over the world.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信