PO.ET02.12 · 实验与分子治疗

YT-DP: A glyco-conjugation-based dual-payloads ADC platform

海报缩略图:YT-DP: A glyco-conjugation-based dual-payloads ADC platform
编号 3083 展板 11 时间 4/20 02:00–05:00 区域 Section 16 主讲 Yi Yang, PhD
分会场 Novel Therapeutics and Drug Targets 2
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作者与单位

Yi Yang, Zhentao Song, Rui Yu, Jiangping Hu, Zhouyang Qian, Xinyue He, Guoli Yang, Ji Chen, Juntao Yu

Glyco-therapy Biotechnology Co. Ltd., Hangzhou, China

摘要 Abstract

Dual-payloads antibody-drug conjugates (ADCs) represent a promising next-generation modality to enhance antitumor efficacy, achieve synergistic effects, and overcome tumor heterogeneity and therapeutic resistance. However, their development faces several key challenges, including: (i) identifying payload combinations that maintain efficacy within a shared safety window without single-agent dominance; (ii) achieving precise and efficient assembly of distinct payloads into antibodies with controlled drug-to-antibody ratios (DARs); and (iii) ensuring robust stability, in vivo efficacy, and favorable safety profiles. To address these challenges, we developed YT-DP, a glyco-conjugation-based dual-payloads ADC platform that enables the incorporation of two distinct mechanism-of-action (MOA) payloads into a single antibody molecule through a one-step glyco-conjugation strategy. This system allows flexible DAR configurations (e.g., DAR 2+2 or DAR 2+4). The YT-DP platform integrates our proprietary cleavable-linker-topoisomerase I inhibitor payload (CLTp) technology (YT-CLTp) with a microtubule inhibitor (MTI) via the YTConju glyco-conjugation system. The YT-CLTp series comprises tunable payload candidates with adjustable target and bystander killing activities, demonstrating superior anti-tumor potency compared with “GGFG-Dxd” in multiple CDX models when conjugated to antibodies. We generated trastuzumab-based dual-payloads ADCs (Tras-DPs) containing an MTI and distinct CLTps at different DARs (DAR 2+2 and DAR 2+4). Tras-DPs exhibited high homogeneity, excellent thermal and plasma stability, and potent synergistic antitumor activity with strong by-stander effects. Notably, Tras-DPs demonstrated markedly superior antitumor activity compared with DS-8201, as well as the corresponding single-payload ADCs or their combinations, in CDX models. In addition, the dual-payloads ADCs showed favorable pharmacokinetic (PK) properties and safety profiles in rat studies. In summary, the YT-DP platform provides a robust and versatile strategy for constructing homogeneous, stable, and synergistic dual-payloads ADCs with tunable DARs. Its broad compatibility with various antibody formats, including Fc-containing bispecific antibodies, underscores its potential to enable next-generation ADCs with an enhanced therapeutic index.
利益披露 Disclosure
Y. Yang, None.. Z. Song, None.. R. Yu, None.. J. Hu, None.. Z. Qian, None.. X. He, None.. G. Yang, None.. J. Chen, None.. J. Yu, None.

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