An IQ Industry Perspective on Informing Dosing Recommendations in Patients With Renal Impairment.

IF 6.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Clinical Pharmacology & Therapeutics Pub Date : 2025-02-01 Epub Date: 2024-10-22 DOI:10.1002/cpt.3463
Ashish Sharma, Islam R Younis, Jitendra Kanodia, Vaishali Sahasrabudhe
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引用次数: 0

Abstract

The IQ CPLG Organ Impairment WG conducted a survey to understand how various IQ member companies develop dosing recommendations for patients with renal impairment. Eighteen IQ member companies participated in the survey. The survey results were summarized by the working group in light of the regulatory renal impairment guidance documents as well as recent publications from the pharmaceutical industry and nephrology community. There were two important learnings from the survey: (i) pharmaceutical companies do not use a consistent methodology to assess renal function in their drug development programs. (ii) there has been significant improvement in predicting how kidney function affects drug pharmacokinetics (PK) and thus dose recommendations. Applying model-based methods such as population PK, physiologically-based PK (PBPK), and virtual controls has enabled earlier prediction of how kidney function influences PK, leading to the participation of more patients with impaired kidney function in Phase 2 and 3 trials.

从智商行业的角度看肾功能受损患者的用药建议。
IQ CPLG 器官损伤工作组进行了一项调查,以了解各 IQ 成员公司如何为肾功能损伤患者制定用药建议。18 家 IQ 成员公司参与了调查。工作组根据监管部门的肾功能损害指导文件以及制药行业和肾病学界最近的出版物对调查结果进行了总结。调查有两个重要发现:(i) 制药公司在药物开发项目中没有使用统一的方法来评估肾功能。(ii) 在预测肾功能如何影响药物药代动力学 (PK) 以及剂量建议方面已经取得了重大进展。应用基于模型的方法,如群体 PK、基于生理的 PK (PBPK) 和虚拟对照,可以更早地预测肾功能对 PK 的影响,从而让更多肾功能受损的患者参与 2 期和 3 期试验。
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来源期刊
CiteScore
12.70
自引率
7.50%
发文量
290
审稿时长
2 months
期刊介绍: Clinical Pharmacology & Therapeutics (CPT) is the authoritative cross-disciplinary journal in experimental and clinical medicine devoted to publishing advances in the nature, action, efficacy, and evaluation of therapeutics. CPT welcomes original Articles in the emerging areas of translational, predictive and personalized medicine; new therapeutic modalities including gene and cell therapies; pharmacogenomics, proteomics and metabolomics; bioinformation and applied systems biology complementing areas of pharmacokinetics and pharmacodynamics, human investigation and clinical trials, pharmacovigilence, pharmacoepidemiology, pharmacometrics, and population pharmacology.
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