利用探索性药代动力学和药效学分析,预测健康志愿者和慢性乙型肝炎患者接受收费样受体7激动剂鲁佐唑莫德治疗后出现流感样症状的概率。

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Qiudi Jiang, Yuchen Zhang, Dan Duan, Sylvie Retout, Ruchi Upmanyu, Katerina Glavini, Miriam Triyatni, Yonghong Zhu, Joseph F. Grippo, Yuyan Jin
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引用次数: 0

摘要

Ruzotolimod(Toll 样受体 7 (TLR7) 激动剂,RG7854)是一种激活 TLR 7 的口服小分子免疫调节剂,目前正在 CHB 患者中进行评估。与其他 TLR7 激动剂一样,在 Ruzotolimod 的 I 期研究中,一些参与者出现了与研究药物相关的流感样症状不良事件。我们对两项 I 期研究的参与者进行了药代动力学(PK)/药效学(PD)与流感样症状之间关系的探索性分析,这些参与者包括健康志愿者和接受单次或多次递增剂量口服鲁佐替莫德的 NUC 抑制型 CHB 患者。线性回归和逻辑回归用于探讨剂量、流感样症状、PK 和 PD 之间的潜在关系。采用广义线性回归预测在不同的 RO7011785(双原药鲁索托莫德的活性代谢产物)PK 暴露下出现各种强度流感样症状的概率。该分析表明,单次或多次服用 Ruzotolimod ⩾100 毫克时,免疫 PD(IFN-α、新蝶呤、IP-10 和 ISG15、OAS-1、MX1 和 TLR7 的转录表达)反应随 RO7011785 PK 暴露量的增加而增加,而 RO7011785 PK 暴露量随 Ruzotolimod 剂量从 3 毫克到 170 毫克的增加而呈线性增加。分析还显示,流感样症状发生的概率随着PD反应(IFN-α和IP-10)的增加而增加。减少鲁佐唑莫德的剂量可以有效降低PD反应的程度,从而降低对PD激活高度敏感和对流感样症状不耐受的参与者在所有强度下出现与研究药物相关的流感样症状的概率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Using exploratory pharmacokinetic and pharmacodynamic analyses to predict the probability of flu-like symptoms in healthy volunteers and patients with chronic hepatitis B treated with the toll-like receptor 7 agonist ruzotolimod

Using exploratory pharmacokinetic and pharmacodynamic analyses to predict the probability of flu-like symptoms in healthy volunteers and patients with chronic hepatitis B treated with the toll-like receptor 7 agonist ruzotolimod

Ruzotolimod (Toll-like receptor 7 (TLR7) agonist, RG7854) is an oral, small molecule immuno-modulator activating the TLR 7 and is being evaluated in patients with CHB. As with other TLR7 agonists, the study drug-related adverse events of flu-like symptoms have been reported in some participants during phase I studies with ruzotolimod. An exploratory analysis of the relationship between pharmacokinetic (PK)/pharmacodynamic (PD) and flu-like symptoms was performed in participants from two phase I studies including both healthy volunteers and NUC-suppressed CHB patients who received either single or multiple ascending doses of orally administered ruzotolimod. Linear and logistic regression were used to explore potential relationships between dose, flu-like symptoms, PK, and PD. Generalized linear regression was performed to predict the probability of flu-like symptoms of all intensities at different RO7011785 (the active metabolite of the double prodrug ruzotolimod) PK exposure. This analysis showed that single or multiple doses of ruzotolimod at ⩾100 mg, the immune PD (IFN-α, neopterin, IP-10, and the transcriptional expression of ISG15, OAS-1, MX1, and TLR7) responses increase with the RO7011785 PK exposure, which increases linearly with the doses from 3 mg to 170 mg of ruzotolimod. The analysis also showed that the probability of flu-like symptoms occurrence increases with PD responses (IFN-α and IP-10). Dose reduction of ruzotolimod can be an effective way to reduce the magnitude of PD response, thus reducing the probability of study drug-related flu-like symptoms occurrence at all intensity in the participants who are highly sensitive to PD activation and intolerant to flu-like symptoms.

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来源期刊
Cts-Clinical and Translational Science
Cts-Clinical and Translational Science 医学-医学:研究与实验
CiteScore
6.70
自引率
2.60%
发文量
234
审稿时长
6-12 weeks
期刊介绍: Clinical and Translational Science (CTS), an official journal of the American Society for Clinical Pharmacology and Therapeutics, highlights original translational medicine research that helps bridge laboratory discoveries with the diagnosis and treatment of human disease. Translational medicine is a multi-faceted discipline with a focus on translational therapeutics. In a broad sense, translational medicine bridges across the discovery, development, regulation, and utilization spectrum. Research may appear as Full Articles, Brief Reports, Commentaries, Phase Forwards (clinical trials), Reviews, or Tutorials. CTS also includes invited didactic content that covers the connections between clinical pharmacology and translational medicine. Best-in-class methodologies and best practices are also welcomed as Tutorials. These additional features provide context for research articles and facilitate understanding for a wide array of individuals interested in clinical and translational science. CTS welcomes high quality, scientifically sound, original manuscripts focused on clinical pharmacology and translational science, including animal, in vitro, in silico, and clinical studies supporting the breadth of drug discovery, development, regulation and clinical use of both traditional drugs and innovative modalities.
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