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April 5, 2026Cancer Research1 citations

Abstract 6926: An AI-guided biparatopic DLL3-targeting ADC demonstrates enhanced preclinical efficacy

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CCChuan ChenYWYue WuCSChenpeng Su

Key Points

  • The aim is to develop an effective biparatopic ADC targeting DLL3 for small cell lung cancer and neuroendocrine neoplasms.
  • Engineered a biparatopic anti-DLL3 antibody using an AI-guided platform.
  • Conjugated the antibody with various linker-payload combinations.
  • Evaluated in vitro cytotoxicity in DLL3-expressing cell lines.
  • Assessed in vivo efficacy using CDX mice models.
  • Conducted safety assessments in transgenic mice and non-human primates.
  • The biparatopic antibody showed higher internalization efficiency than monoclonal counterparts.
  • Demonstrated potent cytotoxicity in multiple DLL3-expressing cell lines.
  • Achieved significant tumor suppression in CDX models.
  • Exhibited a favorable safety profile in transgenic mice and non-human primates.

Abstract

Abstract Purpose: This study aimed to develop a novel biparatopic antibody-drug conjugate (ADC) targeting delta-like ligand 3 (DLL3) for small cell lung cancer (SCLC) and other neuroendocrine neoplasms, addressing limitations of previous DLL3-targeted therapies. Methods: Leveraging our AI-guided antibody development platform, we engineered a biparatopic anti-DLL3 antibody with optimized binding and internalization properties. The antibody was conjugated with various linker-payload combinations. In vitro cytotoxicity of the ADCs were evaluated using DLL3-expressing cell lines and in vivo efficacy were assessed using CDX mice models. Safety was assessed in transgenic mice and non-human primates. Results: The biparatopic antibody demonstrated higher internalization efficiency compared to the monoclonal antibody counterparts. The ADC showed potent cytotoxicity across multiple DLL3-expressing cell lines and achieved significant tumor suppression in CDX models. Toxicological studies revealed a favorable safety profile in both transgenic mice and non-human primates. Conclusion: This biparatopic ADC represents a promising therapeutic candidate for DLL3-expressing tumors, demonstrating enhanced efficacy and favorable preclinical safety compared to previous approaches. Citation Format: Chuan Chen, Yue Wu, Chenpeng Su, Zhaohui Chen, Dandan Liu, Jiyuan Tian, Xiaoqian Chen, Yang He, Yongxin Shang, Rongmei Yan, Liang Tian, Jian Peng, Zhenping Zhu, . An AI-guided biparatopic DLL3-targeting ADC demonstrates enhanced preclinical efficacy abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6926.

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Cite This Study

Chen et al. (2026) studied this question.

synapsesocial.com/papers/69d1fceba79560c99a0a2a85https://doi.org/10.1158/1538-7445.am2026-6926
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Abstract 5406: A novel AI-engineered biparatopic DLL3/CD3 T cell engager demonstrates potent preclinical efficacy and a promising safety profile.2026
  2. 2Abstract 1708: Novel DLL3 x B7H3 bispecific ADC demonstrated superior efficacy in preclinical studies2026
  3. 3Abstract LB193: A novel DLL3-B7H3 bispecific dual-payload ADC, KHN928, demonstrates potent antitumor efficacy in small cell lung cancer2026
  4. 4Abstract 1717: SCR-A014, a novel bispecific ADC targeting B7H3 and DLL3 for SCLC therapy, exhibits potent anti-tumor efficacy2026
  5. 5DB-1314, a novel DLL3-targeting ADC with DNA topoisomerase I inhibitor, exhibits promising safety profile and therapeutic efficacy in preclinical small cell lung cancer models2024 · 23 citations