Novel Patient-Friendly Orodispersible Formulation of Ivermectin is Associated With Enhanced Palatability, Controlled Absorption, and Less Variability: High Potential for Pediatric Use

Kim Dao MD, Michael Buettcher MD, Klervi Golhen PharmD, MSc, Jonas Kost MSc, Andreas Schittny PhD, Urs Duthaler PhD, Andrew Atkinson PhD, David Haefliger MD, Monia Guidi PhD, Carine Bardinet MSc, Haithem Chtioui MD, Abdelwahab Boulekbache MD, Thierry Buclin MD, Jörg Huwyler PhD, Marc Pfister MD, Laura E. Rothuizen MD
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Abstract

Ivermectin has been used since the 1980s as an anthelmintic and antiectoparasite agent worldwide. Currently, the only available oral formulation is tablets designed for adult patients. A patient-friendly orodispersible tablet formulation designed for pediatric use (CHILD-IVITAB) has been developed and is entering early phase clinical trials. To inform the pediatric program of CHILD-IVITAB, 16 healthy adults were enrolled in a phase I, single-center, open-label, randomized, 2-period, crossover, single-dose trial which aimed to compare palatability, tolerability, and bioavailability and pharmacokinetics of CHILD-IVITAB and their variability against the marketed ivermectin tablets (STROMECTOL) at a single dose of 12 mg in a fasting state. Palatability with CHILD-IVITAB was considerably enhanced as compared to STROMECTOL. Both ivermectin formulations were well tolerated and safe. Relative bioavailability of CHILD-IVITAB compared to STROMECTOL was estimated as the ratios of geometric means for Cmax, AUC 0-∞, and AUC0-last, which were 1.52 [90% CI: 1.13-2.04], 1.27 [0.99-1.62], and 1.29 [1.00-1.66], respectively. Maximum drug concentrations occurred earlier with the CHILD-IVITAB formulation, with a median Tmax at 3.0 h [range 2.0-4.0 h] versus 4.0 h [range 2.0-5.0 h] with STROMECTOL (P = .004). With CHILD-IVITAB, variability in exposure was cut in half (coefficient of variation: 37% vs 70%) compared to STROMECTOL. Consistent with a more controlled absorption process, CHILD-IVITAB was associated with reduced variability in drug exposure as compared to STROMECTOL. Together with a favorable palatability and tolerability profile, these findings motivate for further clinical studies to evaluate benefits of such a patient-friendly ODT formulation in pediatric patients with a parasitic disease, including infants and young children <15 kg.

Abstract Image

伊维菌素的新型患者友好型可分散制剂具有更强的适口性、可控吸收性和更小的变异性:在儿科应用中潜力巨大。
伊维菌素自 20 世纪 80 年代以来一直作为一种驱虫药和抗线虫药在世界各地使用。目前,唯一可用的口服制剂是为成人患者设计的片剂。一种专为儿科设计、方便患者使用的口服分散片剂型(CHILD-IVITAB)已经开发出来,并进入早期临床试验阶段。为了给 CHILD-IVITAB 的儿科项目提供信息,16 名健康成人参加了一项 I 期、单中心、开放标签、随机、2 期、交叉、单剂量试验,目的是比较 CHILD-IVITAB 的适口性、耐受性、生物利用度和药代动力学,以及它们与市场上销售的伊维菌素片剂(STROMECTOL)在空腹状态下单次剂量为 12 毫克时的差异。与 STROMECTOL 相比,CHILD-IVITAB 的适口性大大提高。两种伊维菌素制剂都具有良好的耐受性和安全性。与 STROMECTOL 相比,CHILD-IVITAB 的相对生物利用度按 Cmax、AUC 0-∞ 和 AUC0-last 的几何平均比估算,分别为 1.52 [90% CI:1.13-2.04]、1.27 [0.99-1.62] 和 1.29 [1.00-1.66]。CHILD-IVITAB制剂的最大药物浓度出现较早,中位Tmax为3.0小时[范围2.0-4.0小时],而STROMECTOL为4.0小时[范围2.0-5.0小时](P = .004)。与 STROMECTOL 相比,CHILD-IVITAB 的暴露变异性降低了一半(变异系数:37% 对 70%)。与更可控的吸收过程相一致,CHILD-IVITAB 与 STROMECTOL 相比,降低了药物暴露的变异性。再加上良好的适口性和耐受性,这些发现推动了进一步的临床研究,以评估这种方便患者的 ODT 制剂在儿童寄生虫病患者(包括婴幼儿)中的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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