Antibody Information
General Information of This Antibody
Antibody ID | ANI0LNFRO |
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Antibody Name | huAb3v2.6 |
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Antibody Type | Monoclonal antibody (mAb) |
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Antibody Subtype | Humanized IgG1-kappa |
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Antigen Name | CD276 antigen (CD276) |
Antigen Info |
Each Antibody-drug Conjugate Related to This Antibody
Full Information of The Activity Data of The ADC(s) Related to This Antibody
huAb3v2.6-XW [Investigative]
Discovered Using Cell Line-derived Xenograft Model
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) |
43.00%
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
Humanized anti-B7-H3 antibodies huAb13v1, huAb3v2.5 and huAb3v2.6 were selected to beconjugated with several Bcl-xL inhibitor payloads and were evaluated in xenograft models of small cell lung cancer (H146). The dose was 6 mg/kg/IP/QDx1.
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In Vivo Model | H146 CDX model | ||||
In Vitro Model | Small cell carcinoma | NCI-H146 cells | CVCL_1473 |
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
2.40 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-AAA [Investigative]
Discovered Using Cell Line-derived Xenograft Model
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) |
47.00%
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
Humanized anti-B7-H3 antibodies huAb13v1, huAb3v2.5 and huAb3v2.6 were selected to beconjugated with several Bcl-xL inhibitor payloads and were evaluated in xenograft models of small cell lung cancer (H146). The dose was 6 mg/kg/IP/QDx1.
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In Vivo Model | H146 CDX model | ||||
In Vitro Model | Small cell carcinoma | NCI-H146 cells | CVCL_1473 | ||
Experiment 2 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) |
50.00%
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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 3 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) |
60.00%
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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) |
63.00%
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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 5 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) |
92.00%
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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 6 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) |
99.00%
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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 7 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) |
99.00%
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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) |
1.24 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-TX [Investigative]
Discovered Using Cell Line-derived Xenograft Model
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) |
92.00%
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
Humanized anti-B7-H3 antibodies huAb13v1, huAb3v2.5 and huAb3v2.6 were selected to beconjugated with several Bcl-xL inhibitor payloads and were evaluated in xenograft models of small cell lung cancer (H146). The dose was 6 mg/kg/IP/QDx1.
|
||||
In Vivo Model | H146 CDX model | ||||
In Vitro Model | Small cell carcinoma | NCI-H146 cells | CVCL_1473 |
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
0.47 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-CZ [Investigative]
Discovered Using Cell Line-derived Xenograft Model
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) |
93.00%
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
Humanized anti-B7-H3 antibodies huAb13v1, huAb3v2.5 and huAb3v2.6 were selected to beconjugated with several Bcl-xL inhibitor payloads and were evaluated in xenograft models of small cell lung cancer (H146). The dose was 6 mg/kg/IP/QDx1.
|
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In Vivo Model | H146 CDX model | ||||
In Vitro Model | Small cell carcinoma | NCI-H146 cells | CVCL_1473 |
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) |
1.70 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the H847 cell line. IC50 values were determined by quantitating viable cells using a CellTiter-Glo luminescent assay.
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In Vitro Model | Lung small cell carcinoma | NCI-H847 cells | CVCL_1596 | ||
Experiment 2 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
0.40 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-TV [Investigative]
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
0.52 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-YG [Investigative]
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
0.68 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-SR [Investigative]
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
0.71 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-YY [Investigative]
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
0.72 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-WD [Investigative]
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
0.79 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-AAD [Investigative]
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
0.85 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-SE [Investigative]
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
1.01 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-ZT [Investigative]
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
1.11 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-ZZ [Investigative]
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
1.35 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-LB [Investigative]
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
2.07 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
huAb3v2.6-KZ [Investigative]
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Effective Concentration (EC50) |
5.52 nM
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Positive CD276 expression (CD276 +++/++) | ||
Method Description |
The anti-tumor activity of these ADCs was tested in cytotoxicity assaysusing the NCI-H1650 non-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 | Lung adenocarcinoma | NCI-H1650 cells | CVCL_1483 |
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