General Information of This Antibody-drug Conjugate (ADC)
ADC ID
DRG0JQMLE
ADC Name
wO2023232144A1ADC-2
Synonyms
WO2023232144A1ADC-2
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Organization
GeneQuantum Healthcare (Suzhou) Co. Ltd.
Drug Status
Investigative
Drug-to-Antibody Ratio
3.8
Structure
Antibody Name
anti-HER2 antibody mAb-1
 Antibody Info 
Antigen Name
Receptor tyrosine-protein kinase erbB-2 (ERBB2)
 Antigen Info 
Payload Name
WO2023232144A1, ADC-2, Payload
 Payload Info 
Therapeutic Target
DNA topoisomerase I (TOP1)
 Target Info 
Linker Name
WO2023232144A1, ADC-2, linker
 Linker Info 
Combination Type
LP-6
ADC-specific functional property(2027 Update)
Circulating Stability
Click To Hide/Show 4 ADC-specific functional property Data
Incubation Time 0h Release 100% Reference
[1]
Incubation Medium The change rates of DAR
Description
When ADC-2 was incubated in healthy mixed human plasma for 0,24,48 and 96 h, the change rates of DAR were 100.00%, 106.7%, 104.2% and 106.5%, respectively. The shedding ratio of small molecular toxins was 0.006%, 0.179%, 0.373% and 1.07%, respectively.

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Incubation Time 24h Release 106.7% Reference
[1]
Incubation Medium The change rates of DAR
Description
When ADC-2 was incubated in healthy mixed human plasma for 0,24,48 and 96 h, the change rates of DAR were 100.00%, 106.7%, 104.2% and 106.5%, respectively. The shedding ratio of small molecular toxins was 0.006%, 0.179%, 0.373% and 1.07%, respectively.

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Incubation Time 48h Release 104.2% Reference
[1]
Incubation Medium The change rates of DAR
Description
When ADC-2 was incubated in healthy mixed human plasma for 0,24,48 and 96 h, the change rates of DAR were 100.00%, 106.7%, 104.2% and 106.5%, respectively. The shedding ratio of small molecular toxins was 0.006%, 0.179%, 0.373% and 1.07%, respectively.

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Incubation Time 96h Release 106.5% Reference
[1]
Incubation Medium The change rates of DAR
Description
When ADC-2 was incubated in healthy mixed human plasma for 0,24,48 and 96 h, the change rates of DAR were 100.00%, 106.7%, 104.2% and 106.5%, respectively. The shedding ratio of small molecular toxins was 0.006%, 0.179%, 0.373% and 1.07%, respectively.

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Bystander Killing Effect
Click To Hide/Show 1 ADC-specific functional property Data
Bystander Killing Effect Description Reference
no Undisclosed
[1]
General Information of The Activity Data Related to This ADC
Revealed Based on the Cell Line Data
Click To Hide/Show 2 Activity Data Related to This Level
Standard Type Value Units Cell Line Disease Model
Half Maximal inhibitory Concentration (lC50) 
0.1076
nM
CVCL_0033
Breast adenocarcinoma
Half Maximal inhibitory Concentration (lC50) 
0.4355
nM
CVCL_1259
Breast ductal carcinoma
Full List of Activity Data of This Antibody-drug Conjugate
Revealed Based on the Cell Line Data
Click To Hide/Show 2 Activity Data Related to This Level
Experiment 1 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal inhibitory Concentration (lC50) 0.1076 nM Positive ErbB2/HER2 expression (ErbB2/HER2+++/++)
Method Description
Cytotoxicity of ADC-2 to SK-BR-3 cells
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) 0.4355 nM Positive ErbB2/HER2 expression (ErbB2/HER2+++/++)
Method Description
Cytotoxicity of ADC to HCC1954 cells
In Vitro Model Breast ductal carcinoma HCC1954 cells CVCL_1259
References
Ref 1 Oligosaccharide linkers, linker-payloads comprising the linkers, and glycan chain-remodeled antibody-drug conjugates, preparation methods and uses thereof