Abstract Introduction: The epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor 3 (HER3) are frequently co-expressed in a variety of solid tumors and play crucial roles in driving tumor growth, therapeutic resistance, and metastasis. To overcome the limitations of single-target approaches, we developed a novel bispecific antibody-drug conjugate simultaneously targeting EGFR and HER3. Methods: HDM2024 was engineered using single-valency design, consists of a clinically validated HER3 antibody paired with an EGFR-targeting VHH antibody. The antibody was conjugated with exatecan via a cleavable linker, drug-antibody ratio (DAR) is 4. The efficacy and safety of HDM2024 were tested in xenograft and patient derived xenograft (PDX) models and monkeys, respectively. Results: HDM2024 was designed with balanced affinity towards EGFR and HER3 antigen. In vitro, HDM2024 demonstrated high-affinity binding to both EGFR and HER3 expressing tumor cells, efficient internalization, and potent cytotoxicity across a panel of cancer cell lines with varying expression levels of EGFR and HER3. In vivo, HDM2024 exhibited robust antitumor efficacy in multiple xenograft and patient-derived xenograft (PDX) models, achieving complete or durable tumor regressions at well-tolerated doses. In GLP toxicity study, HDM2024 showed favorable safety with the highest non-severely toxic dose (HNSTD) reaching up to 40mg/kg administered every 2weeks (Q2W) for three cycles. Conclusion: Collectively, these results support HDM2024 as a promising therapeutic candidate for solid cancer treatment. A differentiated ADC drug design endows HDM2024 with enhanced pharmacological efficacy and safety advantages, giving it the potential to become a best-in-class drug candidate. HDM2024 is expected to start the clinical trial in Mar 2026. Citation Format: Qingyu Shu, Yan Xia, Zhaofeng Qin, Shengxing Zhao, Yang Chen, Rongrong He, Hao Pan, Hongwen Li, Dongzhou Jeffrey Liu, . HDM2024: A novel EGFR and HER3 bispecific antibody-drug conjugate exhibits superior antitumor activity and favorable toxicological profile 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 6945.
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Shu et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69d1fe07a79560c99a0a47ee — DOI: https://doi.org/10.1158/1538-7445.am2026-6945
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
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