Abstract 1681: RenLite® transgenic mice provide a high-quality platform for accelerating the development of fully human bispecific antibodies or ADCs worldwide

Abstract Global development of bispecific antibodies (BsAbs) and bispecific antibody-drug conjugates (BsADCs) is undergoing explosive growth. However, key pain points persist—heavy-light chain mismatch, inadequate target synergy, poor toxicity control, and complex manufacturing. While novel technologies have been developed to address these issues, drug development still faces hurdles in target combination selection, lengthy antibody discovery cycles, and low clinical translation success rates. Biocytogen RenLite® mice generate fully human antibody candidates with a common light chain, enabling subsequent assembly of BsAbs with minimized chain mismatch and excellent developability—conferring advantages for downstream CMC development. Additionally, the common light chain facilitates screening of different BsAb formats, payload conjugation, and function evaluation—supporting the discovery of diverse BsAb or BsAb-ADC modalities. To date, leveraging RenLite® and its novel BsADC platform, Biocytogen has generated multiple preclinical BsAb-ADC candidates. For example, DM001 (anti-TROP2×EGFR), with good developability, demonstrates potent tumor-suppressive activity in seven various patient-derived xenograft (PDX) models; DM005 (anti-EGFR×MET), with high purity and good conjugation property, exhibits outstanding specificity and anti-tumor efficacy in lung cancer PDX models. These BsADC candidates hold great clinical development potential. Leveraging its RenLite® platform and preliminary screening, Biocytogen has built an antibody library covering over 200 tumor-associated antigens (TAAs). This lets researchers easily conduct rapid screening, flexible pairing, and target synergy validation using in vitro/in vivo efficacy platforms, speeding up BsAb/ BsADC development and boosting clinical translation success of anticancer therapies. Citation Format: Jade Hsu, Wenjiao Zhang, Jun Du, Zhuolin Li, Yifu Zhang, Yanfei Han, Chengzhang Shang, Yi Yang, . RenLite® transgenic mice provide a high-quality platform for accelerating the development of fully human bispecific antibodies or ADCs worldwide [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 1681.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-1681
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
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article

Abstract 1681: RenLite® transgenic mice provide a high-quality platform for accelerating the development of fully human bispecific antibodies or ADCs worldwide

Zhuolin Li, Yanfei Han, Yifu Zhang, Jade Hsu et al.
Cancer Research
Monoclonal and Polyclonal Antibodies Research
article

Abstract 1681: RenLite® transgenic mice provide a high-quality platform for accelerating the development of fully human bispecific antibodies or ADCs worldwide

Zhuolin Li, Yanfei Han, Yifu Zhang, Jade Hsu, Chengzhang Shang, Yi Yang, Jun Du, Wenjiao Zhang
article en

Abstract

Abstract Global development of bispecific antibodies (BsAbs) and bispecific antibody-drug conjugates (BsADCs) is undergoing explosive growth. However, key pain points persist—heavy-light chain mismatch, inadequate target synergy, poor toxicity control, and complex manufacturing. While novel technologies have been developed to address these issues, drug development still faces hurdles in target combination selection, lengthy antibody discovery cycles, and low clinical translation success rates. Biocytogen RenLite® mice generate fully human antibody candidates with a common light chain, enabling subsequent assembly of BsAbs with minimized chain mismatch and excellent developability—conferring advantages for downstream CMC development. Additionally, the common light chain facilitates screening of different BsAb formats, payload conjugation, and function evaluation—supporting the discovery of diverse BsAb or BsAb-ADC modalities. To date, leveraging RenLite® and its novel BsADC platform, Biocytogen has generated multiple preclinical BsAb-ADC candidates. For example, DM001 (anti-TROP2×EGFR), with good developability, demonstrates potent tumor-suppressive activity in seven various patient-derived xenograft (PDX) models; DM005 (anti-EGFR×MET), with high purity and good conjugation property, exhibits outstanding specificity and anti-tumor efficacy in lung cancer PDX models. These BsADC candidates hold great clinical development potential. Leveraging its RenLite® platform and preliminary screening, Biocytogen has built an antibody library covering over 200 tumor-associated antigens (TAAs). This lets researchers easily conduct rapid screening, flexible pairing, and target synergy validation using in vitro/in vivo efficacy platforms, speeding up BsAb/ BsADC development and boosting clinical translation success of anticancer therapies. Citation Format: Jade Hsu, Wenjiao Zhang, Jun Du, Zhuolin Li, Yifu Zhang, Yanfei Han, Chengzhang Shang, Yi Yang, . RenLite® transgenic mice provide a high-quality platform for accelerating the development of fully human bispecific antibodies or ADCs worldwide [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 1681.

Cancer ResearchVol. 86(7_Supplement)
Beijing Biocytogen (China) (CN)
No poverty
Openalex Percentile: Top 5%
Monoclonal and Polyclonal Antibodies Research
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