Abstract 2395: DXC011, a novel dual-payload antibody-drug conjugate targeting folate receptor alpha.

Abstract Folate Receptor alpha (FRα) is highly expressed in epithelial ovarian cancer and selected solid tumors, making it an attractive target for antibody-drug conjugates (ADCs). Although an FRα-directed ADC Elahere has already achieved clinical approval, this microtubule inhibitor-based agent faces challenges, such as ocular toxicity, narrow therapeutic windows, and limited activity beyond ovarian cancer. To address these limitations, we developed DXC011, a next-generation FRα-targeting ADC engineered to enhance antitumor efficacy while improving tolerability. DXC011 comprises DXA011, a humanized IgG1 antibody specific for FRα, an optimized cleavable linker and a dual functional payload. This dual-payload strategy introduces complementary cytotoxic mechanisms and may help overcome resistance associated with single-mechanism ADCs. DXC011 demonstrated potent activity across multiple FRα-expressing in vitro and in vivo tumor models, encompassing ovarian cancer as well as additional solid tumor types. Beyond established ovarian cancer settings, DXC011 showed notable efficacy in gastrointestinal tumor models, supporting its potential for broader clinical application. Moreover, DXC011 displayed favorable tolerability in mouse, with an improved safety profile relative to microtubule inhibitor-based ADC while maintaining robust antitumor potency. Collectively, these findings indicate that DXC011 offers an improved therapeutic index and may enable expanded indication coverage. DXC011 represents a novel FRα-targeted dual-payload ADC that achieves potent and broad antitumor activity with enhanced tolerability, supporting its advancement toward clinical development. Citation Format: Zhicang Ye, Huihui Guo, Wei Zheng, Junpeng Wang, Yifang Xu, Hui Xia, Yuanyuan Huang, Junxiang Jia, Wei Liu, Xiang Chen, You Zhou, Qingliang Yang, Robert Y. Zhao. DXC011, a novel dual-payload antibody-drug conjugate targeting folate receptor alpha [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 2395.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-2395
Primary Topic
HER2/EGFR in Cancer Research
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article
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article

Abstract 2395: DXC011, a novel dual-payload antibody-drug conjugate targeting folate receptor alpha.

Qingliang Yang, You Lang Zhou, Zhicang Ye, Junpeng Wang et al.
Cancer Research
HER2/EGFR in Cancer Research
article

Abstract 2395: DXC011, a novel dual-payload antibody-drug conjugate targeting folate receptor alpha.

Qingliang Yang, You Lang Zhou, Zhicang Ye, Junpeng Wang, Hui Xia, Wei Liu, Wei Zheng, Yuanyuan Huang, Robert Y. Zhao, Yifang Xu, Xiang Chen, Junxiang Jia, Huihui Guo
article en

Abstract

Abstract Folate Receptor alpha (FRα) is highly expressed in epithelial ovarian cancer and selected solid tumors, making it an attractive target for antibody-drug conjugates (ADCs). Although an FRα-directed ADC Elahere has already achieved clinical approval, this microtubule inhibitor-based agent faces challenges, such as ocular toxicity, narrow therapeutic windows, and limited activity beyond ovarian cancer. To address these limitations, we developed DXC011, a next-generation FRα-targeting ADC engineered to enhance antitumor efficacy while improving tolerability. DXC011 comprises DXA011, a humanized IgG1 antibody specific for FRα, an optimized cleavable linker and a dual functional payload. This dual-payload strategy introduces complementary cytotoxic mechanisms and may help overcome resistance associated with single-mechanism ADCs. DXC011 demonstrated potent activity across multiple FRα-expressing in vitro and in vivo tumor models, encompassing ovarian cancer as well as additional solid tumor types. Beyond established ovarian cancer settings, DXC011 showed notable efficacy in gastrointestinal tumor models, supporting its potential for broader clinical application. Moreover, DXC011 displayed favorable tolerability in mouse, with an improved safety profile relative to microtubule inhibitor-based ADC while maintaining robust antitumor potency. Collectively, these findings indicate that DXC011 offers an improved therapeutic index and may enable expanded indication coverage. DXC011 represents a novel FRα-targeted dual-payload ADC that achieves potent and broad antitumor activity with enhanced tolerability, supporting its advancement toward clinical development. Citation Format: Zhicang Ye, Huihui Guo, Wei Zheng, Junpeng Wang, Yifang Xu, Hui Xia, Yuanyuan Huang, Junxiang Jia, Wei Liu, Xiang Chen, You Zhou, Qingliang Yang, Robert Y. Zhao. DXC011, a novel dual-payload antibody-drug conjugate targeting folate receptor alpha [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 2395.

Cancer ResearchVol. 86(7_Supplement)
Hangzhou DAC Biotech (China) (CN)
Good health and well-being
Openalex Percentile: Top 7%
HER2/EGFR in Cancer Research
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