Advancing Subcutaneous Delivery: Evaluation of Near-Body Auto-Injector Systems for High-Volume Biologic Administration with Human Hyaluronidase: Poster Presented at PDA Week 2026.

Q3 Medicine
Kallie Johnson, Ryan Wangsnes, Baylor Frantz, Robert J Connor, Tara Nekoroski, Kevin D Swanson, David W Kang
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引用次数: 0

Abstract

Subcutaneous (SC) delivery of biologics is evolving to accommodate the greater volumes and doses required for efficacy. Conventional handheld auto-injectors are constrained by volume and speed limitations, prompting the development of high-volume auto-injectors (HVAIs) and wearable on-body injectors (OBI). A Near-Body Injector (NBI) system offers a novel approach by combining the benefits of high-volume delivery with hands-free operation, without the need for adhesive attachment associated with OBI's by using a standard winged infusion set and a mechanical priming mechanism incorporated into the device. This study evaluated the feasibility of a NBI system in a porcine model, delivering SC immunoglobulin alone and in combination with recombinant human hyaluronidase PH20 (rHuPH20), an enzyme known to enhance SC dispersion and absorption.Results demonstrated that the NBI system was easily primed and effectively delivered 10 mL SC. Co-formulation with rHuPH20 significantly improved injection performance, reducing delivery time by ∼13%, eliminating back-leakage, and decreasing swelling volume and induration at the injection site. These findings support the clinical potential of NBI systems for hands-free high-volume, high-dose biologic administration, offering an alternative to conventional SC delivery methods.

推进皮下给药:评估人体透明质酸酶大剂量生物给药的近体自动注射系统:在PDA周2026上发表的海报。
生物制剂的皮下递送正在不断发展,以适应更大的体积和疗效所需的剂量。传统的手持式自动注射器受到体积和速度的限制,促使了大容量自动注射器(HVAIs)和可穿戴式身体注射器(OBI)的发展。近体注射器(NBI)系统提供了一种新颖的方法,它结合了大容量输送和免提操作的优点,而不需要与OBI相关的粘合剂连接,使用标准的翼形输液器和机械启动机制。本研究在猪模型中评估了NBI系统的可行性,该系统单独递送SC免疫球蛋白,并与重组人透明质酸酶PH20 (rHuPH20)联合递送,这种酶可以增强SC的分散和吸收。结果表明,NBI系统易于启动并有效递送10 mL SC。与rHuPH20共同配制可显著改善注射性能,将递送时间缩短约13%,消除反漏,减少注射部位的肿胀体积和硬结。这些发现支持了NBI系统在免提大容量、高剂量生物给药方面的临床潜力,为传统的SC给药方法提供了一种替代方案。
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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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
34
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