Antibody-drug Conjugate Information
General Information of This Antibody-drug Conjugate (ADC)
| ADC ID |
DRG0TSYYJ
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| ADC Name |
WO2024193682A1 32G1-8H10-CPT2
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| Synonyms |
32G1-8H10-CPT2
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| Organization |
XADCERA BIOPHARMACEUTICAL (SUZHOU) CO., LTD.
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| Drug Status |
Investigative
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| Antibody Name |
undisclosed
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| Antigen Name |
Trophoblast glycoprotein (TPBG)
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Antigen Info | ||||
| Payload Name |
CPT2
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Payload Info | ||||
| Therapeutic Target |
DNA topoisomerase I (TOP1)
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Target Info | ||||
| Linker Name |
Undisclosed
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General Information of The Activity Data Related to This ADC
Discovered Using Patient-derived Xenograft Model
Full List of Activity Data of This Antibody-drug Conjugate
Discovered Using Patient-derived Xenograft Model
| Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
| Efficacy Data | Tumor Growth lnhibition value (TGl) |
63.10%
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| Method Description |
B-NDG mice were engrafted in the right flank with gastric cancer patient-derived tumortissue fragments (2 mm x 2 mm x 2 mm). The immunofluorescence staining results showed that TPBG-positive cells and MET-positive cells in the gastric tumor fragments were 10.1 1% and 1.19%, respectively, When the tumors in the mice reached a volume of about 200-300 mm3, the mice were randomly placed into different groups based on the tumor volume. The mice werethen injected with 6mg/kg ADC's by i.v, QW, administration. Determined tumor volume after the experiment, measured at day 35.
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| In Vivo Model | Patient-derived Xenograft B-NDG mice Model | ||||
| Experiment 2 Reporting the Activity Date of This ADC | [1] | ||||
| Efficacy Data | Tumor Growth lnhibition value (TGl) |
80.40%
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| Method Description |
B-NDG mice were engrafted in the right flank with pancreatic cancer patient-derivedtumor tissue fragments (2 mm x 2 mm x 2 mm). The immunofluorescence staining results showed that TPGB-positive cells and MET-positive cells in the pancreatic tumor fragments were 31.01% and 76.96%, respectively. When the tumors in the mice reached a volume of about 200-300mm3, the mice were randomly placed into different groups based on the tumor volume. Themice were then injected with 6mg/kg ADC's by i.v, QW, administration. Determined tumor volume after the experiment, measured at day 25.
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| In Vivo Model | Patient-derived Xenograft B-NDG mice Model | ||||
| Experiment 3 Reporting the Activity Date of This ADC | [1] | ||||
| Efficacy Data | Tumor Growth lnhibition value (TGl) |
90.90%
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| Method Description |
B-NDG mice were engrafted in the right flank with pancreatic cancer patient-derivedtumor tissue fragments (2 mm x 2 mm x 2 mm). The immunofluorescence staining results showed that TPGB-positive cells and MET-positive cells in the pancreatic tumor fragments were 19.54% and 8.31%, respectively. When the tumors in the mice reached a volume of about 200-300 mm3, the mice were randomly placed into different groups based on the tumor volume. Themice were then injected with 3mg/kg ADC's by i.v, BIW, administration. Determined tumor volume after the experiment, measured at day 32.
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| In Vivo Model | Patient-derived Xenograft B-NDG mice Model | ||||
| Experiment 4 Reporting the Activity Date of This ADC | [1] | ||||
| Efficacy Data | Tumor Growth lnhibition value (TGl) |
91.50%
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| Method Description |
B-NDG mice were engrafted in the right flank with pancreatic cancer patient-derivedtumor tissue fragments (2 mm x 2 mm x 2 mm). The immunofluorescence staining results showed that TPGB-positive cells and MET-positive cells in the pancreatic tumor fragments were 58.86% and 24.08%, respectively. When the tumors in the mice reached a volume of about 150-200 mm3, the mice were randomly placed into different groups based on the tumor volume. Themice were then injected with 6mg/kg ADC's by i.v, QW, administration. Determined tumor volume after the experiment, measured at day 25.
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| In Vivo Model | Patient-derived Xenograft B-NDG mice Model | ||||
