Antibody-drug Conjugate Information
General Information of This Antibody-drug Conjugate (ADC)
| ADC ID |
DRG0UBQII
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| ADC Name |
WO2023047090A1-SN-38 reagent (13) ADC
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| Synonyms |
SN-38 reagent (13) ADC
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| Organization |
SPIREA LIMITED
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| Drug Status |
Investigative
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| Drug-to-Antibody Ratio |
20.3
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| Structure |
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| Antibody Name |
Trastuzumab
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Antibody Info | ||||
| Antigen Name |
Receptor tyrosine-protein kinase erbB-2 (ERBB2)
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Antigen Info | ||||
| Payload Name |
Undisclosed
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| Therapeutic Target |
Stimulator of interferon genes protein (STING1)
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Target Info | ||||
| Linker Name |
Undisclosed
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| Conjugate Type |
Random conjugation through reduced inter-chain cysteines.
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| Combination Type |
SN-38 reagent
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ADC-specific functional property(2027 Update)
Bystander Killing Effect
| Bystander Killing Effect | Description | Reference |
|---|---|---|
| no | Undisclosed |
[1]
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Circulating Stability
| Incubation Time | 96hours | Release | 50-55% | Reference |
[1]
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| Incubation Medium | mouse plasma | ||||
| Description |
ADCs were spiked into mouse plasma and incubated at 37°C over a 96h period. To evaluate thechanges in DAR profile throughout plasma incubation, ADCs were analysed by HIC-UV (214nm)after isolation from plasma using affinity capture.
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General Information of The Activity Data Related to This ADC
Full List of Activity Data of This Antibody-drug Conjugate
Revealed Based on the Cell Line Data
| Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) | 0.04 nM | High HER2 expression (HER2 +++) | ||
| Method Description |
1250cells/well for SK-BR-3 (100 uL) of cells were seeded onto 384-well plates and incubated for 24 hours before adding the ADC. After 9 hours, the limited exposure treated plates were removed from the incubator and media containing compound was removed. Cells were washed 2x with growth medium and 40 uL growth medium was then added to each well. Plates were incubated at 37 °C/5% CO, for a further 96 hours. 40uL of CellTiter-Glo reagent was added to each well to be tested (the ratio of CellTiter-Glo reagent to medium was 1:1).the plate was then placed at room temperature for 30 minutes, and then reading was carried out on an EnSpire reader for cell counting.
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| In Vitro Model | Breast adenocarcinoma | SK-BR-3 cells | CVCL_0033 | ||
| Experiment 2 Reporting the Activity Date of This ADC | [1] | ||||
| Efficacy Data | Half Maximal inhibitory Concentration (lC50) | 0.18 nM | High HER2 expression (HER2 +++) | ||
| Method Description |
1250cells/well for SK-BR-3 (100 uL) of cells were seeded onto 384-well plates and incubated for 24 hours before adding the ADC. After 9 hours, the limited exposure treated plates were removed from the incubator and media containing compound was removed. 40uL of CellTiter-Glo reagent was added to each well to be tested (the ratio of CellTiter-Glo reagent to medium was 1:1).the plate was then placed at room temperature for 30 minutes, and then reading was carried out on an EnSpire reader for cell counting.
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| In Vitro Model | Breast adenocarcinoma | SK-BR-3 cells | CVCL_0033 | ||
