• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一项在局部应用硬脂酰辅酶 A 去饱和酶 1 抑制剂的条件下进行的 1 期随机、安慰剂对照试验,包括封闭和非封闭条件。

A Phase 1 Randomized, Placebo-Controlled Trial With a Topical Inhibitor of Stearoyl-Coenzyme A Desaturase 1 Under Occluded and Nonoccluded Conditions.

机构信息

Virtual Proof of Concept Discovery Performance Unit, GlaxoSmithKline, King of Prussia, PA, USA.

Clinical Pharmacology Modeling and Simulation, GlaxoSmithKline, King of Prussia, PA, USA.

出版信息

Clin Pharmacol Drug Dev. 2019 Apr;8(3):270-280. doi: 10.1002/cpdd.644. Epub 2019 Jan 16.

DOI:10.1002/cpdd.644
PMID:30650256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6590436/
Abstract

Stearoyl-coenzyme A desaturase 1 (SCD-1) in sebaceous glands is a key enzyme in the synthesis of monounsaturated fatty acids essential for acne development. GSK1940029 gel, a novel SCD-1 inhibitor, is being developed as a potential treatment for acne. To assess the irritation potential, pharmacokinetics (PK), and safety of topical GSK1940029 to the skin of healthy adults, two interdependent studies were conducted in parallel. Study 1 (n = 54) investigated the irritation potential of GSK1940029 (0.3% and 1%, occluded application) to allow for its application to larger surface areas in study 2 (n = 39), which investigated the safety, tolerability, and PK of GSK1940029 after single and repeat doses as occluded and nonoccluded applications. GSK1940029 was not a primary or cumulative irritant after 2 and 21 days of dosing in study 1. In study 2, single and repeat applications of GSK1940029 (0.1% to 1%) doses were well tolerated with little or no influence on AUC and C under occluded or unoccluded conditions. Systemic exposure increased proportionally with surface area and was higher in occluded conditions. Design of these interdependent studies allowed for the assessment of the irritation potential for topical GSK1940029 in parallel with the investigation of PK and safety profiles.

摘要

皮脂腺中的硬脂酰辅酶 A 去饱和酶 1(SCD-1)是合成单不饱和脂肪酸的关键酶,单不饱和脂肪酸是痤疮发展所必需的。GSK1940029 凝胶是一种新型的 SCD-1 抑制剂,被开发为一种治疗痤疮的潜在药物。为了评估 GSK1940029 对健康成年人皮肤的潜在刺激性、药代动力学(PK)和安全性,进行了两项相互依存的研究。研究 1(n=54)研究了 GSK1940029(0.3%和 1%,封闭应用)的刺激性,以便在研究 2(n=39)中更大面积应用,该研究评估了 GSK1940029 单次和重复剂量作为封闭和非封闭应用的安全性、耐受性和 PK。在研究 1 中,GSK1940029 在 2 天和 21 天给药后既不是原发性也不是累积性刺激物。在研究 2 中,GSK1940029(0.1%至 1%)单次和重复应用在封闭和非封闭条件下均具有良好的耐受性,对 AUC 和 C 几乎没有或没有影响。在封闭和非封闭条件下,系统暴露与表面积成正比增加,且在封闭条件下更高。这些相互依存的研究设计允许在并行评估局部 GSK1940029 的刺激性潜力的同时,研究 PK 和安全性概况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6238/6590436/39d04ded280e/CPDD-8-270-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6238/6590436/b3372abd85d1/CPDD-8-270-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6238/6590436/84f78d19b60c/CPDD-8-270-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6238/6590436/7eec19207292/CPDD-8-270-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6238/6590436/8a1822ac67a2/CPDD-8-270-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6238/6590436/39d04ded280e/CPDD-8-270-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6238/6590436/b3372abd85d1/CPDD-8-270-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6238/6590436/84f78d19b60c/CPDD-8-270-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6238/6590436/7eec19207292/CPDD-8-270-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6238/6590436/8a1822ac67a2/CPDD-8-270-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6238/6590436/39d04ded280e/CPDD-8-270-g005.jpg

相似文献

1
A Phase 1 Randomized, Placebo-Controlled Trial With a Topical Inhibitor of Stearoyl-Coenzyme A Desaturase 1 Under Occluded and Nonoccluded Conditions.一项在局部应用硬脂酰辅酶 A 去饱和酶 1 抑制剂的条件下进行的 1 期随机、安慰剂对照试验,包括封闭和非封闭条件。
Clin Pharmacol Drug Dev. 2019 Apr;8(3):270-280. doi: 10.1002/cpdd.644. Epub 2019 Jan 16.
2
Pharmacological inhibition of stearoyl CoA desaturase in the skin induces atrophy of the sebaceous glands.皮肤中硬脂酰辅酶A去饱和酶的药理抑制会导致皮脂腺萎缩。
J Invest Dermatol. 2013 Aug;133(8):2091-4. doi: 10.1038/jid.2013.89. Epub 2013 Feb 27.
3
Randomized, Double-Blind, Split-Face Study to Compare the Irritation Potential of Two Topical Acne Formulations Over a 21-Day Treatment Period.一项随机、双盲、半脸对照研究,旨在比较两种外用痤疮制剂在21天治疗期内的潜在刺激性。
J Drugs Dermatol. 2016 Feb;15(2):178-82.
4
An overview of patented small molecule stearoyl coenzyme-A desaturase inhibitors (2009 - 2013).专利小分子硬脂酰辅酶A去饱和酶抑制剂概述(2009 - 2013年)
Expert Opin Ther Pat. 2014 Feb;24(2):155-75. doi: 10.1517/13543776.2014.851669. Epub 2013 Nov 20.
5
Pharmacokinetics of tazarotene cream 0.1% after a single dose and after repeat topical applications at clinical or exaggerated application rates in patients with acne vulgaris or photodamaged skin.0.1%他扎罗汀乳膏在寻常痤疮或光损伤皮肤患者中单次给药后以及以临床或超量应用频率重复局部给药后的药代动力学。
Clin Pharmacokinet. 2003;42(10):921-9. doi: 10.2165/00003088-200342100-00004.
6
Tretinoin gel microspheres 0.04% versus 0.1% in adolescents and adults with mild to moderate acne vulgaris: a 12-week, multicenter, randomized, double-blind, parallel-group, phase IV trial.0.04%与0.1%维甲酸凝胶微球治疗青少年和成人轻至中度寻常痤疮的12周多中心随机双盲平行组IV期试验
Clin Ther. 2007 Jun;29(6):1086-97. doi: 10.1016/j.clinthera.2007.06.021.
7
Two Randomized, Double-Blind, Split-Face Studies to Compare the Irritation Potential of Two Topical Acne Fixed Combinations Over a 21-Day Treatment Period.两项随机、双盲、半脸对照研究,旨在比较两种外用痤疮固定复方制剂在21天治疗期内的潜在刺激性。
J Drugs Dermatol. 2016 Jun 1;15(6):721-6.
8
Clinical Pharmacokinetics, Safety and Exploratory Efficacy Study of a Topical Bactericidal VB-1953: Analysis of Single and Multiple Doses in a Phase I Trial in Acne Vulgaris Subjects.一项用于治疗寻常痤疮的局部杀菌 VB-1953 的临床药代动力学、安全性和探索性疗效研究:I 期临床试验中单剂量和多剂量的分析。
Clin Drug Investig. 2020 Mar;40(3):259-268. doi: 10.1007/s40261-019-00883-5.
9
Safety and Pharmacokinetics of Once-Daily Dapsone Gel, 7.5% in Patients With Moderate Acne Vulgaris.每日一次使用7.5%氨苯砜凝胶治疗中度寻常痤疮患者的安全性和药代动力学
J Drugs Dermatol. 2016 Oct 1;15(10):1250-1259.
10
Regulation of stearoyl-coenzyme A desaturase and fatty acid delta-6 desaturase-2 expression by linoleic acid and arachidonic acid in human sebocytes leads to enhancement of proinflammatory activity but does not affect lipogenesis.亚油酸和花生四烯酸对人皮脂腺细胞中硬脂酰辅酶 A 去饱和酶和脂肪酸 delta-6 去饱和酶-2 表达的调节导致促炎活性增强,但不影响脂生成。
Br J Dermatol. 2011 Aug;165(2):269-76. doi: 10.1111/j.1365-2133.2011.10340.x. Epub 2011 Jun 30.

引用本文的文献

1
Highly Multiplexed Tissue Imaging in Precision Oncology and Translational Cancer Research.精准肿瘤学和转化癌症研究中的高多重组织成像。
Cancer Discov. 2024 Nov 1;14(11):2071-2088. doi: 10.1158/2159-8290.CD-23-1165.
2
Stearoyl-CoA desaturase 1 inhibition induces ER stress-mediated apoptosis in ovarian cancer cells.硬脂酰辅酶 A 去饱和酶 1 抑制诱导卵巢癌细胞内质网应激介导的细胞凋亡。
J Ovarian Res. 2024 Apr 2;17(1):73. doi: 10.1186/s13048-024-01389-1.
3
Targeting cancer metabolism in the era of precision oncology.精准肿瘤学时代的肿瘤代谢靶向治疗。

本文引用的文献

1
Recent progress in the discovery and development of stearoyl CoA desaturase inhibitors.硬脂酰辅酶A去饱和酶抑制剂发现与开发的最新进展
Chem Phys Lipids. 2016 May;197:3-12. doi: 10.1016/j.chemphyslip.2015.08.018. Epub 2015 Sep 3.
2
The use of isotretinoin in the treatment of acne vulgaris: clinical considerations and future directions.异维A酸在寻常痤疮治疗中的应用:临床考量与未来方向。
J Clin Aesthet Dermatol. 2014 Feb;7(2 Suppl):S3-S21.
3
Microclimate next to the skin: influence on percutaneous absorption of caffeine (ex-vivo study).
Nat Rev Drug Discov. 2022 Feb;21(2):141-162. doi: 10.1038/s41573-021-00339-6. Epub 2021 Dec 3.
皮肤附近的微气候:对咖啡因经皮吸收的影响(体外研究)
Skin Res Technol. 2014 Aug;20(3):293-8. doi: 10.1111/srt.12118. Epub 2013 Dec 12.
4
Are Food and Drug Administration prescription drug safety plans working? A case study of isotretinoin.美国食品药品监督管理局的处方药安全计划有效吗?异维甲酸案例研究。
Pharmacoepidemiol Drug Saf. 2013 Dec;22(12):1258-62. doi: 10.1002/pds.3514. Epub 2013 Sep 22.
5
The development and registration of topical pharmaceuticals.局部用药物制剂的开发和注册。
Int J Pharm. 2012 Oct 1;435(1):22-6. doi: 10.1016/j.ijpharm.2012.03.052. Epub 2012 Apr 3.
6
Pathogenesis of acne vulgaris: what's new, what's interesting and what may be clinically relevant.寻常痤疮的发病机制:新进展、有趣之处及临床相关要点
J Drugs Dermatol. 2011 Jun;10(6):582-5.
7
Can sebum reduction predict acne outcome?皮脂减少能否预测痤疮的结局?
Br J Dermatol. 2010 Oct;163(4):683-8. doi: 10.1111/j.1365-2133.2010.09878.x.
8
The key roles of elongases and desaturases in mammalian fatty acid metabolism: Insights from transgenic mice.长链烯酰基辅酶 A 合酶和去饱和酶在哺乳动物脂肪酸代谢中的关键作用:来自转基因小鼠的研究进展。
Prog Lipid Res. 2010 Apr;49(2):186-99. doi: 10.1016/j.plipres.2009.12.002. Epub 2009 Dec 16.
9
New insights into the management of acne: an update from the Global Alliance to Improve Outcomes in Acne group.痤疮管理的新见解:改善痤疮结局全球联盟小组的最新进展
J Am Acad Dermatol. 2009 May;60(5 Suppl):S1-50. doi: 10.1016/j.jaad.2009.01.019.