PO.ET02.07 · 实验与分子治疗

NEU-002的转化开发:工程化治疗性弹性蛋白酶通过腹腔内和静脉给药展现出全身性抗肿瘤活性

Translational development of NEU-002: Engineered therapeutic elastases demonstrate systemic anti-tumor activity via intraperitoneal and intravenous administration

编号 310 展板 28 时间 4/19 02:00–05:00 区域 Section 13 主讲 Peter Haberz
分会场 Innovative Therapeutic Modalities and Translational Platforms
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作者与单位 Authors & Affiliations

Maria Fumagalli, Chang Cui, Ravindra Gujar, Nicole Martinez, Peter Haberz, Court Turner, Lev Becker

Onchilles Pharma Inc, San Diego, CA

摘要 Abstract

中文摘要
NEU-002是一种可全身递送的工程化弹性蛋白酶,靶向ELANE通路,正在针对实体瘤进行开发。为推动NEU-002走向临床转化,通过理性序列工程生成了两个优化候选物N17474和N17482。这一优化策略聚焦于通过防止丝氨酸蛋白酶抑制剂的作用来保留弹性蛋白酶在血液中的活性,并使用一系列生化实验进行评估。此外,我们表明NEU-002项目化合物在静脉给药后于CT26结肠癌模型中维持了强劲的抗肿瘤疗效,证明在优化过程中保留了关键的功能特性。另外,我们探索了一种新的腹腔内给药途径以扩展NEU-002的递送选择,并在原位结肠癌小鼠模型中观察到肿瘤负荷的降低,支持了触及内脏腔室内肿瘤的可行性。总的来说,这些发现为NEU-002确立了坚实的转化基础,并且连同计划在非人灵长类动物中开展的药代动力学研究,将直接为最终开发候选物的选择提供依据,以推进其在实体瘤适应症中的临床评估。 本摘要在文本起草过程中使用了生成式人工智能辅助。
查看英文原文 English abstract
NEU-002 is a systemically deliverable engineered elastase targeting the ELANE pathway and is under development for solid tumors. To advance NEU-002 toward clinical translation, two optimized candidates, N17474 and N17482, were generated through rational sequence engineering. This optimization strategy focused on preserving elastase activity in blood by protection from serine protease inhibitors, as evaluated using a range of biochemical assays. Furthermore, we show that NEU-002 program compounds maintained robust anti-tumor efficacy in the CT26 colon cancer model following intravenous administration, demonstrating that essential functional properties were retained during optimization. In addition, we explored a new intraperitoneal route of administration to expand delivery options for NEU-002 and observed reductions in tumor burden in orthotopic colon cancer mouse models, supporting the feasibility of accessing tumors within visceral compartments. Collectively, these findings establish a strong translational foundation for NEU-002 and, together with planned pharmacokinetic studies in non-human primates, will directly inform the selection of the final development candidate for advancement toward clinical evaluation in solid tumor indications. Generative artificial intelligence was used to assist in drafting text for this abstract.
利益披露 Disclosure
M. Fumagalli, None.. C. Cui, None.. R. Gujar, None.. N. Martinez, None.. P. Haberz, None.. C. Turner, None.. L. Becker, None.

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