• 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

进食对健康受试者利沃赛尼血药浓度的影响。

Effect of food intake on the pharmacokinetics of rivoceranib in healthy subjects.

机构信息

Elevar Therapeutics, Inc., Salt Lake City, UT, USA.

DUCK FLATS Pharma, Flemington, NJ, USA.

出版信息

Fundam Clin Pharmacol. 2022 Feb;36(1):171-181. doi: 10.1111/fcp.12707. Epub 2021 Jul 6.

DOI:10.1111/fcp.12707
PMID:34101892
Abstract

Rivoceranib is a selective inhibitor of VEGFR-2 being developed for the treatment of solid tumor. The objective of the study was to evaluate the effect of food on bioavailability as well as single- and multiple-dose pharmacokinetics (PKs) of 81 and 201 mg doses of rivoceranib. The study was conducted as a two-part study. In Part 1 (single ascending dose (SAD), open-label, crossover study design), 2 oral doses of rivoceranib (81 mg or 201 mg) were given to all healthy subjects with a minimum 3-day washout period between dosing. Part 2 was a multiple ascending dose (MAD), open-label, crossover design where subjects were divided based on 81 and 201 mg doses. Both doses were administered with and without food in a crossover manner for the SAD and MAD parts. 24 healthy subjects completed Part 1 and 20 subjects completed Part 2. For the 81 mg dose in the SAD and MAD parts of the study, their food effect was not observed. For the 201 mg dose in both parts, food appeared to increase bioavailability by 20%-30% in Part 1, and 30%-40% in Part 2. Median t value was delayed when rivoceranib was administered with food at each dose level in both parts of the study. Dose proportionality was confirmed only for the AUC  value from Part 1-fasted cohort but inconclusive for C  and AUC parameters under other dosing regimens. In conclusion, rivoceranib when taken with food delays t appears to increase bioavailability at 201 mg dose.

摘要

里沃卡尼伯是一种选择性血管内皮生长因子受体-2 抑制剂,用于治疗实体瘤。本研究的目的是评估食物对 81mg 和 201mg 剂量里沃卡尼伯生物利用度以及单剂量和多剂量药代动力学(PK)的影响。该研究分为两部分进行。在第一部分(单次递增剂量(SAD)、开放标签、交叉设计研究)中,所有健康受试者接受了 2 种口服剂量的里沃卡尼伯(81mg 或 201mg),两次给药之间至少有 3 天的洗脱期。第二部分是一个多递增剂量(MAD)、开放标签、交叉设计,根据 81mg 和 201mg 剂量将受试者进行分组。SAD 和 MAD 部分均以交叉方式给予两种剂量,有或无食物。24 名健康受试者完成了第一部分,20 名受试者完成了第二部分。在研究的 SAD 和 MAD 部分,81mg 剂量没有观察到食物的影响。对于 201mg 剂量,在两部分中,食物似乎使生物利用度增加了 20%-30%,在第二部分中增加了 30%-40%。在研究的两部分中,当里沃卡尼伯与食物一起给药时,每个剂量水平的中位 t 值均延迟。仅在第一部分-禁食队列的 AUC 值中证实了剂量比例性,但在其他给药方案下的 C 和 AUC 参数下结论不确定。总之,里沃卡尼伯与食物一起服用时,t 值延迟,似乎增加了 201mg 剂量的生物利用度。

相似文献

1
Effect of food intake on the pharmacokinetics of rivoceranib in healthy subjects.进食对健康受试者利沃赛尼血药浓度的影响。
Fundam Clin Pharmacol. 2022 Feb;36(1):171-181. doi: 10.1111/fcp.12707. Epub 2021 Jul 6.
2
Effects of Single and Multiple Ascending Doses of BI 1358894 in Healthy Male Volunteers on Safety, Tolerability and Pharmacokinetics: Two Phase I Partially Randomised Studies.单次及多次递增剂量的BI 1358894对健康男性志愿者安全性、耐受性及药代动力学的影响:两项I期部分随机研究
CNS Drugs. 2023 Dec;37(12):1081-1097. doi: 10.1007/s40263-023-01041-4. Epub 2023 Nov 29.
3
A randomized phase I study to evaluate the safety, tolerability, pharmacokinetics and food-effect of Iguratimod in healthy adult volunteers.一项评估艾拉莫德在健康成年志愿者中的安全性、耐受性、药代动力学及食物影响的随机I期研究。
Eur J Clin Pharmacol. 2018 Jan;74(1):69-77. doi: 10.1007/s00228-017-2342-z. Epub 2017 Oct 19.
4
Effects of Food Intake on the Relative Bioavailability of Amifampridine Phosphate Salt in Healthy Adults.食物摄入对健康成年人中磷酸阿米芬啶相对生物利用度的影响。
Clin Ther. 2015 Jul 1;37(7):1555-63. doi: 10.1016/j.clinthera.2015.05.498. Epub 2015 Jun 20.
5
Pharmacokinetics of a New Amphetamine Extended-release Oral Liquid Suspension Under Fasted and Fed Conditions in Healthy Adults: A Randomized, Open-label, Single-dose, 3-treatment Study.健康成年人禁食和进食条件下新型苯丙胺缓释口服液的药代动力学:一项随机、开放标签、单剂量、3 种治疗方案研究。
Clin Ther. 2017 Dec;39(12):2389-2398. doi: 10.1016/j.clinthera.2017.10.018. Epub 2017 Nov 23.
6
A Randomized, Crossover Study on the Effect of Food on the Pharmacokinetic Characteristics of Morphine ARER (MorphaBond™ ER), an Abuse-Deterrent Formulation of Extended-Release Morphine.一项关于食物对吗啡 ARER(MorphaBond™ ER)药代动力学特征影响的随机、交叉研究,吗啡 ARER 是一种延长释放吗啡的、具有防滥用配方的制剂。
Adv Ther. 2019 Sep;36(9):2394-2401. doi: 10.1007/s12325-019-01022-4. Epub 2019 Jul 5.
7
Differential pharmacokinetics of diclofenac potassium for oral solution vs immediate-release tablets from a randomized trial: effect of fed and fasting conditions.随机试验中口服溶液与普通片的双氯芬酸钾的药代动力学差异:进食与禁食状态的影响。
Headache. 2015 Feb;55(2):265-75. doi: 10.1111/head.12483. Epub 2014 Dec 24.
8
Safety, tolerability and pharmacokinetics of trimebutine 3-thiocarbamoylbenzenesulfonate (GIC-1001) in a randomized phase I integrated design study: single and multiple ascending doses and effect of food in healthy volunteers.3-硫代氨基甲酰基苯磺酸盐曲美布汀(GIC-1001)在一项随机I期整合设计研究中的安全性、耐受性和药代动力学:健康志愿者的单次和多次递增剂量以及食物的影响
Clin Ther. 2014 Nov 1;36(11):1650-64. doi: 10.1016/j.clinthera.2014.08.005. Epub 2014 Sep 15.
9
Absence of ethnic difference on single-dose pharmacokinetics of rivoceranib between healthy male Caucasian, Japanese, and Chinese subjects.健康白种人、日本人和中国人男性单次给药药代动力学无种族差异。
Fundam Clin Pharmacol. 2021 Apr;35(2):485-495. doi: 10.1111/fcp.12619. Epub 2020 Nov 9.
10
Single and Multiple Ascending-dose Studies of Oral Delafloxacin: Effects of Food, Sex, and Age.口服德拉氟沙星的单次和多次递增剂量研究:食物、性别和年龄的影响。
Clin Ther. 2016 Jan 1;38(1):39-52. doi: 10.1016/j.clinthera.2015.10.016. Epub 2015 Nov 12.

引用本文的文献

1
A Phase II Trial of Rivoceranib, an Oral Vascular Endothelial Growth Factor Receptor 2 Inhibitor, for Recurrent or Metastatic Adenoid Cystic Carcinoma.一项评估 Rivoceranib(一种口服血管内皮生长因子受体 2 抑制剂)治疗复发性或转移性腺样囊性癌的 II 期临床试验。
Clin Cancer Res. 2023 Nov 14;29(22):4555-4563. doi: 10.1158/1078-0432.CCR-23-1030.
2
Fast-Fed Variability: Insights into Drug Delivery, Molecular Manifestations, and Regulatory Aspects.快速给药变异性:药物递送、分子表现及监管方面的见解
Pharmaceutics. 2022 Aug 27;14(9):1807. doi: 10.3390/pharmaceutics14091807.