Antibody-drug Conjugate Information
General Information of This Antibody-drug Conjugate (ADC)
ADC ID |
DRG0ELNEW
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ADC Name |
Bispecific nBT062-natalizumab-DM4
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Synonyms |
Bispecific nBT062 natalizumab DM4
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Drug Status |
Investigative
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Indication |
In total 2 Indication(s)
Breast cancer [ICD11:2C60-2C65]
Investigative
Multiple myeloma [ICD11:2A83]
Investigative
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Drug-to-Antibody Ratio |
3-4
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Antibody Name |
Bispecific nBT062-natalizumab
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Antibody Info | ||||
Antigen Name |
Syndecan-1 (SDC1); Integrin alpha-4 (ITGA4)
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Antigen Info | ||||
Payload Name |
Mertansine DM4
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Payload Info | ||||
Therapeutic Target |
Microtubule (MT)
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Target Info | ||||
Linker Name |
N-succinimidyl 4-(2-pyridyldithio) butanoate (SPDB)
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Linker Info | ||||
Conjugate Type |
Random conjugation through nucleophilic lysines.
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Combination Type |
Ravtansine
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General Information of The Activity Data Related to This ADC
Discovered Using Patient-derived Xenograft Model
Standard Type | Value | Units | Animal Model (No. of PDX) |
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Tumor Growth Inhibition value (TGI) |
≈ 51.6
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%
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Breast cancer PDX model (PDX: MAXF 1322)
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Revealed Based on the Cell Line Data
Standard Type | Value | Units | Cell Line | Disease Model |
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Half Maximal Inhibitory Concentration (IC50) |
0.46
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nM
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NCI-H929 cells
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Plasma cell myeloma
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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 Inhibition value (TGI) | ≈ 51.60% (Day 56) | Positive CD138 expression (CD138+++/++) | ||
Method Description |
Bispecific nBT062-natalizumab-DM4 (4 mg/kg/week for three injections in total) induces efficient tumor cell killing in models of MAXF1322 mammary carcinoma cells with CD138 expression with high expression.
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In Vivo Model | Breast cancer PDX model (PDX: MAXF 1322) |
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) | 0.46 nM | Positive CD138 expression (CD138+++/++) | ||
Method Description |
WT nBT062-DM4, stable nBT062-DM4, half nBT062-DM4 or bispecific nBT062-natalizumab-DM4 were added to the cells. Cells were incubated and after 5 days the viability was determined using the WST-1 cell proliferation assay.
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In Vitro Model | Plasma cell myeloma | NCI-H929 cells | CVCL_1600 |
References
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