Bispecific ADCs targeting dual tumor-associated antigens (TAAs) enhance cancer treatment by overcoming drug resistance, improving tumor specificity, boosting internalization for better tumor killing, and ensuring stronger, longer-lasting effects in heterogeneous tumors.
Briefly, BLD1102 is a new ADC platform developed by Biocytogen independently.
As part of Biocytogen's Project Integrum, combinations of TAA-targeting antibodies generated from RenLite® mice are subsequently assembled and evaluated in vivo for pharmacologic efficacy, and subjected to in vitro analyses. The company's large animal translational platform will further screen out products with better translational properties:
Target(s) | Immunization |
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CMC | Nonclinical | Phase I | Status |
EGFR x MET (DM005) |
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Partnered | ||||
TROP2 x EGFR (DM001) |
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Partnered | ||||
HER3 x MUC1 (DM002) |
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Partnered | ||||
HER2 x TROP2 (YH012) |
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Partnered | ||||
EGFR x MUC1(BSA01) |
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Partnered | ||||
EGFR x HER3 |
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Partnered | ||||
B7-H3 x PTK7 |
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Partnered | ||||
EGFR x PTK7 |
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SEZ6 x B7-H3 |
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DLL3 x B7-H3 |
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DLL3 x SEZ6 |
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B7-H3 x MUC1 |
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CDH6 x FOLR1 |
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TF(CD142) x NECTIN-4 |
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TF(CD142) x ITGB6 |
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CDH3 x ITGB6 |
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ITGB6 x B7-H3 |
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MUC1 x TROP2 |
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FOLR1 x MUC1 |
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MSLN x FOLR1 |
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MSLN x MUC1 |
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B7-H4 x FOLR1 |
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MET x B7-H3 |
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LGR5 x EGFR |
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