Novartis Pharma AG, Basel, Switzerland.
Novartis Pharmaceuticals, East Hanover, NJ, USA.
Ther Innov Regul Sci. 2024 Mar;58(2):286-302. doi: 10.1007/s43441-023-00599-x. Epub 2023 Dec 18.
The kidneys play a pivotal role in elimination of most drugs; therefore, a comprehensive understanding of renal physiology and pathology is important for those involved in drug development. High filtration capacity and metabolic activity make the kidneys vulnerable to drug-induced nephrotoxicity (DIN). Acute DIN may manifest on a background of renal impairment that has resulted from underlying disease, previously administered nephrotoxic medications, congenital renal abnormalities, or the natural aging process. The ability of the kidneys to compensate for DIN depends on the degree of pre-insult renal function. Therefore, it can be difficult to identify. The discovery and development of novel biomarkers that can diagnose kidney damage earlier and more accurately than current clinical measures and may be effective in detecting DIN. The goal of this manuscript is to provide a pragmatic and evidence-based supportive guidance for the early identification and management of DIN during the drug development process for clinical trial participants of all ages. The overall objective is to minimize the impact of DIN on kidney function and to collect renal safety data enabling risk analysis and mitigation.
肾脏在大多数药物的清除中起着关键作用;因此,对于参与药物开发的人员来说,全面了解肾脏的生理学和病理学非常重要。高滤过能力和代谢活性使肾脏容易受到药物引起的肾毒性(DIN)的影响。急性 DIN 可能在由潜在疾病、先前给予的肾毒性药物、先天性肾脏异常或自然衰老过程引起的肾功能损害的背景下表现出来。肾脏对 DIN 的代偿能力取决于肾损伤前的肾功能程度。因此,DIN 可能难以识别。发现和开发新的生物标志物,这些标志物可以比当前的临床检测更早、更准确地诊断肾脏损伤,并且可能有效检测 DIN,这是本文的目标。本手稿的目的是为药物开发过程中所有年龄段的临床试验参与者提供一种实用的、基于证据的 DIN 早期识别和管理的支持性指导。总体目标是尽量减少 DIN 对肾功能的影响,并收集肾脏安全性数据,以便进行风险分析和缓解。