Antibody-drug Conjugate Information
General Information of This Antibody-drug Conjugate (ADC)
ADC ID |
DRG0DXDHU
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ADC Name |
huAb13v1-WD E2
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Synonyms |
huAb13v1 WD E2; huAb13v1WD E2
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Organization |
AbbVie, Inc.
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Drug Status |
Investigative
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Indication |
In total 1 Indication(s)
Small cell lung cancer [ICD11:2C25]
Investigative
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Drug-to-Antibody Ratio |
2
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Structure | ||||||
Antibody Name |
huAb13v1
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Antibody Info | ||||
Antigen Name |
CD276 antigen (CD276)
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Antigen Info | ||||
Payload Name |
Undisclosed
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Linker Name |
huAb13v1-WD E2 linker
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Combination Type |
AbbVie's WD
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General Information of The Activity Data Related to This ADC
Discovered Using Cell Line-derived Xenograft Model
Revealed Based on the Cell Line Data
Standard Type | Value | Units | Cell Line | Disease Model |
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Half Maximal Effective Concentration (EC50) |
2
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nM
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NCI-H146 cells
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Small cell carcinoma
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Full List of Activity Data of This Antibody-drug Conjugate
Discovered Using Cell Line-derived Xenograft Model
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | 46.00% | Positive CD276 expression (CD276 +++/++) | ||
Method Description |
Humanized anti-B7-H3 antibodies huAb13v1 was selected to beconjugated with several Bcl-xL inhibitor payloads and were evaluated in xenograft models of small cell lung cancer (H1650). The dose was 1 mg/kg/IP/QDx1.
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In Vivo Model | H1650 CDX model | ||||
In Vitro Model | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 | ||
Experiment 2 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | 48.00% | Positive CD276 expression (CD276 +++/++) | ||
Method Description |
Humanized anti-B7-H3 antibodies huAb13v1 was selected to beconjugated with several Bcl-xL inhibitor payloads and were evaluated in xenograft models of small cell lung cancer (H1650). The dose was 3 mg/kg/IP/QDx1.
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In Vivo Model | H1650 CDX model | ||||
In Vitro Model | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 | ||
Experiment 3 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | 56.00% | Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of huAb13vl as CZ or TX conjugates as purified DAR2 (E2)conjugates were characterized in enograft models of non-small cell lung cancer of human origin. The dose was ADC 3 mg/kg (Q14Dx3/IP).
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In Vivo Model | NCI-H1650 CDX model | ||||
In Vitro Model | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 | ||
Experiment 4 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | 60.00% | Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of huAb13vl as CZ or TX conjugates as purified DAR2 (E2)conjugates were characterized in enograft models of non-small cell lung cancer of human origin. The dose was ADC 1 mg/kg (Q14Dx3/IP).
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In Vivo Model | NCI-H1650 CDX model | ||||
In Vitro Model | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 | ||
Experiment 5 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | 62.00% | Positive CD276 expression (CD276 +++/++) | ||
Method Description |
Humanized anti-B7-H3 antibodies huAb13v1 was selected to beconjugated with several Bcl-xL inhibitor payloads and were evaluated in xenograft models of small cell lung cancer (H1650). The dose was 10 mg/kg/IP/QDx1.
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In Vivo Model | H1650 CDX model | ||||
In Vitro Model | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 | ||
Experiment 6 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | 67.00% | Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of huAb13vl as CZ or TX conjugates as purified DAR2 (E2)conjugates were characterized in enograft models of non-small cell lung cancer of human origin. The dose was ADC 10 mg/kg (Q14Dx3/IP).
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In Vivo Model | NCI-H1650 CDX model | ||||
In Vitro Model | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 | ||
Experiment 7 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | 88.00% | Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of huAb13vl as CZ or TX conjugates as purified DAR2 (E2)conjugates were characterized in enograft models of non-small cell lung cancer of human origin. The dose was ADC 1 mg/kg (Q4Dx6/IP) plus Docetaxel 7.5 mg/kg (Q14Dx3/IV).
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In Vivo Model | NCI-H1650 CDX model | ||||
In Vitro Model | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 | ||
Experiment 8 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | 98.00% | Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of huAb13vl as CZ or TX conjugates as purified DAR2 (E2)conjugates were characterized in enograft models of non-small cell lung cancer of human origin. The dose was ADC 10 mg/kg (Q4Dx6/IP) plus Docetaxel 7.5 mg/kg (Q14Dx3/IV).
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In Vivo Model | NCI-H1650 CDX model | ||||
In Vitro Model | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 | ||
Experiment 9 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | 99.00% | Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of huAb13vl as CZ or TX conjugates as purified DAR2 (E2)conjugates were characterized in enograft models of non-small cell lung cancer of human origin. The dose was ADC 3 mg/kg (Q4Dx6/IP) plus Docetaxel 7.5 mg/kg (Q14Dx3/IV).
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In Vivo Model | NCI-H1650 CDX model | ||||
In Vitro Model | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) | 2.00 nM | Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the H146 small cell lung cancer cell line. IC50 values were determined by quantitating viable cells using a CellTiter-Glo luminescent assay.
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In Vitro Model | Small cell carcinoma | NCI-H146 cells | CVCL_1473 |
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