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April 5, 2026Cancer Research0 citations

Abstract 2634: HEC-922:A CDH17-4-1BB bispecific antibody targeting CDH17 positive tumors shows potent anti-tumor activity.

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JDJunji DongSLShushan LinZLZhou Linjun

Key Points

  • The aim is to evaluate the efficacy and safety of HEC-922, a bispecific antibody targeting CDH17 and 4-1BB, in treating CDH17-positive tumors.
  • Development of a bispecific antibody targeting CDH17 and 4-1BB.
  • Assessment of anti-tumor activity in xenograft models of CDH17 positive tumors.
  • Measurement of immune cell function and T cell exhaustion.
  • Evaluation of safety and toxicity profiles.
  • HEC-922 elicited potent tumor growth inhibition in CDH17 positive xenograft models.
  • It activated T cells specifically in the presence of CDH17 positive tumor cells.
  • The antibody demonstrated reduced systemic immune toxicity compared to other 4-1BB agonists.
  • Initial toxicity studies showed favorable safety profiles.

Abstract

Abstract HEC-922 is a novel bispecific agonistic antibody targeting Cadherin-17(CDH17) and the immune agonistic receptor 4-1BB for the treatment of CDH17-positive tumors, particularly gastrointestinal tumors. CDH17 is a tumor associated antigen highly expressed in various tumors, including colorectal cancer, gastric cancer, and neuroendocrine tumors. Activating monoclonal antibodies against 4-1BB have shown clinical efficacy but was limited by systemic toxicity. The design of HEC-922 enables CDH17-dependent agonism of 4-1BB in the presence of CDH17 positive tumor cells, enabling tumor specific T cell activation while minimizing systemic immune toxicity. A high affinity nanobody against CDH17 and a nanobody against 4-1BB were identified for the construction of HEC- 922 containing an ADCC-silenced Fc. HEC-922 shows potent co-binding to both CDH17 and 4-1BB targets and is cross-reactive to the Rhesus macaque. In an assay using 4-1BB high expression 293 cells with NFkB-luciferase reporter, HEC-922 mediated 4-1BB activation in the presence of CDH17 positive cells but not CDH17 negative cells. HEC-922 demonstrated effective tumor growth inhibition in xenograft models of CDH17 positive tumor lines, restored the function of immune cells, reduced the proportion of exhausted T cells, and achieved a sustained and potent anti-tumor effect. Initial drug feasibility and toxicity studies results of HEC-922 were favorable. Overall result demonstrated that HEC- 922 is a promising candidate for CDH17 positive cancer immunotherapy.HEC-921, another bispecific antibody developed on the same 4-1BB platform with Ly6G6D as the targeted tumor antigen, has completed Dose Range Finding (DRF) study in cynomolgus monkeys, with a no-observed-adverse-effect level (NOAEL) of 100 mg/kg, validating the safety of the 4-1BB platform. Citation Format: Junji Dong, Shushan Lin, Zhou Linjun, Jiang Qiuyue, Chen Cangsha, He Shuiqing, Xiang Li, Ju Peng, Xiaohui Li, Cai Zhao, Ming Li, Xiaoping Li, Stewart Leung, . HEC-922:A CDH17-4-1BB bispecific antibody targeting CDH17 positive tumors shows potent anti-tumor activity 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 2634.

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Cite This Study

Dong et al. (2026) studied this question.

synapsesocial.com/papers/69d1fd62a79560c99a0a35ddhttps://doi.org/10.1158/1538-7445.am2026-2634
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