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重组人透明质酸酶 PH20 在非临床模型中的安全性:毒理学、药理学概述及抗 PH20 抗体的影响。

The safety of recombinant human hyaluronidase PH20 in nonclinical models: An overview of toxicology, pharmacology, and impact of anti-PH20 antibodies.

机构信息

Halozyme Therapeutics, Inc., San Diego, CA, USA.

Formerly with Halozyme Therapeutics, Inc., San Diego, CA, USA.

出版信息

J Control Release. 2024 Oct;374:369-383. doi: 10.1016/j.jconrel.2024.07.062. Epub 2024 Aug 23.

Abstract

Hyaluronan (HA) is a glycosaminoglycan that forms a gel-like barrier in the subcutaneous (SC) space, limiting bulk fluid flow and the dispersion of SC-administered therapeutics. Recombinant human hyaluronidase PH20 (rHuPH20) facilitates the rapid delivery of co-administered therapeutics by depolymerizing HA in the SC space. Administration of rHuPH20 can induce the formation of anti-rHuPH20 antibodies, or anti-drug antibodies (ADAs), with the potential to bind endogenous PH20 hyaluronidase in the adult testes and epididymis. Using a variety of relevant animal models and multiple dose regimens of rHuPH20 across the full spectrum of animal development, we demonstrated that rHuPH20 administration resulted in the formation of ADAs. Although these ADAs can bind both the recombinant rHuPH20 enzyme and recombinant versions of animal model-specific hyaluronidases, they had no impact on fertility parameters (as measured by sperm concentration and motility, litter size, and litter viability) or fetal development. We present the result of our nonclinical studies in order of the developmental lifecycle, beginning with adults. Toxicology studies that extend beyond the standard package are also presented. These studies demonstrate the favorable safety profile of rHuPH20 and ADAs in nonclinical models. Additionally, we identified substantial safety margins for clinically relevant doses of rHuPH20.

摘要

透明质酸 (HA) 是一种糖胺聚糖,在皮下 (SC) 空间形成凝胶状屏障,限制了大量流体的流动和 SC 给药治疗药物的扩散。重组人透明质酸酶 PH20(rHuPH20) 通过在 SC 空间中解聚 HA,促进共给药治疗药物的快速递送。rHuPH20 的给药会诱导形成抗 rHuPH20 抗体,或抗药物抗体 (ADA),有可能与成年睾丸和附睾中的内源性 PH20 透明质酸酶结合。使用多种相关动物模型和 rHuPH20 的多种剂量方案,跨越了整个动物发育范围,我们证明了 rHuPH20 给药会导致 ADA 的形成。尽管这些 ADA 可以结合重组 rHuPH20 酶和动物模型特异性透明质酸酶的重组版本,但它们对生育参数(如精子浓度和活力、产仔数和产仔存活率)或胎儿发育没有影响。我们按发育生命周期的顺序介绍了非临床研究结果,首先介绍了成年人。还介绍了超出标准方案的毒理学研究。这些研究表明 rHuPH20 和 ADA 在非临床模型中的安全性良好。此外,我们确定了临床相关剂量的 rHuPH20 的大量安全裕度。

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