Dubowitz Neuromuscular Centre, University College London Institute of Child Health, London, UK.
Summit Therapeutics, Abingdon, UK.
Clin Pharmacol Drug Dev. 2019 Oct;8(7):922-933. doi: 10.1002/cpdd.642. Epub 2019 Jan 16.
Ezutromid (SMT C1100) is a small-molecule utrophin modulator that was developed to treat Duchenne muscular dystrophy (DMD). Previous clinical trials of this agent revealed lower exposure in DMD patients compared with healthy volunteers, which may reflect differences in diet. This study evaluated the pharmacokinetics of ezutromid in patients with DMD who followed a balanced diet. This was a multicenter, double-blind, placebo-controlled, ascending single and multiple oral dose study. Twelve pediatric patients were randomly allocated to 1 of 3 treatment sequences within which were 3 treatment periods of 2 weeks each. Each patient received, in a dose-escalating fashion, 1250 mg and 2500 mg twice daily (BID) of ezutromid administered orally as a microfluidized suspension (F3) with placebo in the other treatment period. Throughout the study, patients followed a balanced diet including recommended proportions of major food groups and administration of drug accompanied with 100 mL of full-fat milk. This approach improved the absorption of ezutromid, resulting in higher systemic exposure, with considerable variability in exposure between patients at each dose level. Single and multiple oral doses of 1250 mg and 2500 mg BID were considered safe and well tolerated. No severe or serious adverse events and no study discontinuations due to adverse events were reported. This study provides assurance that, with the formulation tested (F3) and instructions regarding food (balanced diet and whole-fat milk), 2500 mg BID of ezutromid achieves plasma concentrations that, based on preclinical studies, should be able to modulate utrophin expression in future clinical trials.
依曲替酯(SMT C1100)是一种小分子肌养蛋白调节剂,旨在治疗杜氏肌营养不良症(DMD)。该药物的先前临床试验显示,与健康志愿者相比,DMD 患者的暴露量较低,这可能反映了饮食差异。本研究评估了遵循均衡饮食的 DMD 患者依曲替酯的药代动力学。这是一项多中心、双盲、安慰剂对照、递增单剂量和多剂量口服研究。12 名儿科患者随机分为 3 个治疗序列中的 1 个,每个序列中有 3 个 2 周的治疗期。每个患者以剂量递增的方式接受依曲替酯 1250 mg 和 2500 mg 每日两次(BID),口服微流化混悬液(F3),另一个治疗期给予安慰剂。在整个研究过程中,患者遵循均衡饮食,包括主要食物组的推荐比例,并在服用药物时饮用 100 毫升全脂牛奶。这种方法提高了依曲替酯的吸收,导致系统暴露增加,在每个剂量水平下,患者之间的暴露差异很大。单次和多次口服 1250 mg 和 2500 mg BID 剂量被认为是安全且耐受良好的。未报告严重或严重不良事件,也未因不良事件而停止研究。这项研究提供了保证,使用所测试的制剂(F3)和有关食物(均衡饮食和全脂牛奶)的说明,依曲替酯 2500 mg BID 可达到基于临床前研究,应该能够在未来的临床试验中调节肌养蛋白表达的血浆浓度。