Novaremed AG, Basel, Switzerland.
PK-Insights GmbH, Boeckten, Switzerland.
Clin Pharmacol Drug Dev. 2022 Sep;11(9):1012-1027. doi: 10.1002/cpdd.1103. Epub 2022 Jun 14.
Painful diabetic peripheral neuropathy is characterized by burning, stabbing, or electric shock-type pain, which severely impacts day-to-day functioning and quality of life. Here, we report the results of 3 phase I studies with NRD135S.E1 (referred to as NRD.E1), a new, orally available chemical entity, presently developed for the treatment of painful diabetic peripheral neuropathy. The first study was a first-in-human, randomized, placebo-controlled, single-ascending-dose study, where NRD.E1 was administered to healthy male subjects in single dosages ranging from 300 to 1200 mg. The second study was a randomized, placebo-controlled multiple-dose study, where healthy male subjects received 300 mg of NRD.E1 once daily for 5 consecutive days. The third study was an open-label food interaction study in healthy men and women following a crossover design, where NRD.E1 was administered under fed and fasted conditions at 40 mg. The studies revealed dose-dependent absorption, increased exposure to NRD.E1 when administered with food, and no relevant accumulation after once-daily administration. All 3 phase I studies consistently showed rapid absorption of orally administered NRD.E1 followed by fast elimination, mainly via metabolization (glucuronidation), and small secondary increases in plasma concentrations. NRD.E1 was well tolerated, with no subject discontinuation due to treatment-emergent adverse events in any study.
痛性糖尿病周围神经病变的特征是灼痛、刺痛或电击样疼痛,严重影响日常功能和生活质量。在这里,我们报告了 3 项 I 期临床试验的结果,这些试验是使用一种新的、口服可利用的化学实体 NRD135S.E1(简称 NRD.E1)进行的,目前正在开发用于治疗痛性糖尿病周围神经病变。第一项研究是一项首次人体、随机、安慰剂对照、单次递增剂量研究,在该研究中,健康男性受试者接受了 300 至 1200 毫克单剂量的 NRD.E1 治疗。第二项研究是一项随机、安慰剂对照的多次剂量研究,其中健康男性受试者每天接受 300 毫克 NRD.E1 连续 5 天。第三项研究是一项在健康男性和女性中进行的基于交叉设计的开放标签食物相互作用研究,以 40 毫克的剂量在进食和禁食条件下给予 NRD.E1。这些研究显示了剂量依赖性吸收,与食物同时给予时 NRD.E1 的暴露增加,并且每日一次给药后没有相关的蓄积。所有 3 项 I 期临床试验均一致显示,口服给予的 NRD.E1 吸收迅速,随后消除迅速,主要通过代谢(葡萄糖醛酸化),以及血浆浓度的小幅度二次增加。NRD.E1 耐受性良好,在任何研究中均无因治疗引起的不良事件而导致的受试者停药。