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Results of the First-in-Human Clinical Trial for MB-102, a Novel Fluorescent Tracer Agent for Real-Time Measurement of Glomerular Filtration Rate

机译:实时测量肾小球滤过率的新型荧光示踪剂MB-102的首次人类临床试验结果

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摘要

The fluorescent tracer agent 2,5-bis[N-(1-carboxy-2-hydroxy)]carbamoyl-3,6-diaminopyrazine, designated MB-102, has been developed with properties and attributes necessary for use as a direct measure of glomerular filtration rate (GFR). Comparison to known standard exogenous GFR agents in animal models has demonstrated an excellent correlation. A clinical trial to demonstrate this same correlation in humans is in progress. This clinical trial is the first in a series of trials necessary to obtain regulatory clearance from the FDA. We report herein the comparison of plasma pharmacokinetics between MB-102 and the known standard exogenous GFR agent Iohexol in healthy subjects with normal renal function. Post simultaneous administration of both agents, blood samples over a period of 12 hours were collected from each subject to assess pharmacokinetic parameters including GFR. Urine samples were collected over this same period to assess percent injected dose recovered in the urine. Results indicate MB-102 is a GFR agent in humans from the comparison to the standard agent.
机译:已经开发出荧光示踪剂2,5-双[N-(1-羧基-2-羟基)]氨基甲酰基-3,6-二氨基吡嗪,指定为MB-102,其性质和属性可直接用于测定肾小球滤过率(GFR)。与动物模型中已知的标准外源GFR药剂的比较显示出极好的相关性。正在进行一项临床试验,以证明人类具有相同的相关性。该临床试验是从FDA获得监管批准所必需的一系列试验中的第一个。我们在此报告在肾功能正常的健康受试者中MB-102与已知标准外源性GFR剂Iohexol之间血浆药代动力学的比较。在同时施用两种药剂之后,从每个受试者收集12小时内的血样以评估包括GFR的药代动力学参数。在同一时期收集尿液样品,以评估尿液中回收的注射剂量百分比。结果表明,与标准药物相比,MB-102是人体内的GFR药物。

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