Antibody Information
General Information of This Antibody
Antibody ID | ANI0YJTON |
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Antibody Name | DP001 |
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Antibody Type | Monoclonal antibody (mAb) |
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Antibody Subtype | Humanized IgG1-kappa |
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Antigen Name | Receptor tyrosine-protein kinase erbB-2 (ERBB2) |
Antigen Info |
The Activity Data of This Antibody
Antibody Activity Information 1 | [1] | |||||
Half Maximal Effective Concentration (EC50)
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4.1
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ng/mL
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Antibody Function | Confirm the effect of the drug conjugation with the anti HER2 mAb and ADC on binding activity to cell line. | |||||
Antibody Antigen Binding Assay | The DP303cs affinity for HER2 was determined by ELISA, cell-based assay, and BLI analysis. | |||||
Antibody Activity Information 2 | [1] | |||||
Half Maximal Effective Concentration (EC50)
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124.6
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ng/mL
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SK-BR-3 cells | CVCL_0033 | ||
Antibody Function | Confirm the effect of the drug conjugation with the anti HER2 mAb and ADC on binding activity to cell line. | |||||
Antibody Antigen Binding Assay | The DP303cs affinity for HER2 was determined by ELISA, cell-based assay, and BLI analysis. |
Each Antibody-drug Conjugate Related to This Antibody
Full Information of The Activity Data of The ADC(s) Related to This Antibody
DP-303c [Phase 3]
Identified from the Human Clinical Data
Experiment 1 Reporting the Activity Date of This ADC | [2] | ||||
Related Clinical Trial | |||||
NCT Number | NCT05334810 | Clinical Status | Phase 2 | ||
Clinical Description |
A multi-center, open-lable, single-arm phase 2 study to evaluate the efficacy and safety of DP303c in patients with HER2-positive unresectable locally advanced, relapsed, or metastatic breast cancer.
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Experiment 2 Reporting the Activity Date of This ADC | [3] | ||||
Related Clinical Trial | |||||
NCT Number | NCT04828616 | Clinical Status | Phase 2 | ||
Clinical Description |
An open-label, multicentre, phase 2 study of DP303c injection in patients with HER2-expressing advanced ovarian cancer.
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Experiment 3 Reporting the Activity Date of This ADC | [4] | ||||
Related Clinical Trial | |||||
NCT Number | NCT04826107 | Clinical Status | Phase 2 | ||
Clinical Description |
An open-label, multicentre, phase 2 study of DP303c injection in patients with unresectable locally advanced, recurrent or metastatic gastric cancer with HER2 expression.
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Experiment 4 Reporting the Activity Date of This ADC | [5] | ||||
Related Clinical Trial | |||||
NCT Number | NCT04146610 | Clinical Status | Phase 1 | ||
Clinical Description |
A phase 1a, multicenter, open and dose-increasing study of DP303c to evaluate the safety , pharmacokinetics, immunogenicity and antitumor activity of subjects with HER2-positive advanced solid tumors.
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Discovered Using Cell Line-derived Xenograft Model
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 7.60% (Day 32) | Moderate HER2 expression (HER2++) | ||
Method Description |
DP001 (10 mg/kg).
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In Vivo Model | JIMT -1 cell line xenograft model | ||||
In Vitro Model | Breast ductal carcinoma | JIMT-1 cells | CVCL_2077 | ||
Experiment 2 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 16.20% (Day 32) | Moderate HER2 expression (HER2++) | ||
Method Description |
T-DM1 (10 mg/kg).
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In Vivo Model | JIMT -1 cell line xenograft model | ||||
In Vitro Model | Breast ductal carcinoma | JIMT-1 cells | CVCL_2077 | ||
Experiment 3 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 28.47% (Day 18) | High HER2 expression (HER2+++/++) | ||
Method Description |
DP001 (10 mg/kg).
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In Vivo Model | SK-OV-3 cell line xenograft model | ||||
In Vitro Model | Ovarian serous cystadenocarcinoma | SK-OV-3 cells | CVCL_0532 | ||
Experiment 4 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 33.60% (Day 25) | High HER2 expression (HER2+++/++) | ||
Method Description |
DP001 (10 mg/kg).
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In Vivo Model | NCI-N87 xenograft model | ||||
In Vitro Model | Gastric tubular adenocarcinoma | NCI-N87 cells | CVCL_1603 | ||
Experiment 5 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 39.00% (Day 32) | Moderate HER2 expression (HER2++) | ||
Method Description |
DP303c (0.3 mg/kg).
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In Vivo Model | JIMT -1 cell line xenograft model | ||||
In Vitro Model | Breast ductal carcinoma | JIMT-1 cells | CVCL_2077 | ||
Experiment 6 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 45.26% (Day 18) | High HER2 expression (HER2+++/++) | ||
Method Description |
DP303c (1 mg/kg).
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In Vivo Model | SK-OV-3 cell line xenograft model | ||||
In Vitro Model | Ovarian serous cystadenocarcinoma | SK-OV-3 cells | CVCL_0532 | ||
Experiment 7 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 54.40% (Day 32) | Moderate HER2 expression (HER2++) | ||
Method Description |
Pathogen-free female nude mice were injected subcutaneously with each cell suspension. According to tumor volumes,the mice were randomly divided in two groups: treatment and control groups. Each drug was given to the animals intravenously. The dosing frequency was once a week (qw), qw 2 or qw 3.DP303c induced obvious tumor growth inhibition at a single dose of 0.1 mg/kg.
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In Vitro Model | Breast ductal carcinoma | JIMT-1 cells | CVCL_2077 | ||
Experiment 8 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 82.10% (Day 25) | High HER2 expression (HER2+++) | ||
Method Description |
Pathogen-free female nude mice were injected subcutaneously with each cell suspension. According to tumor volumes,the mice were randomly divided in two groups: treatment and control groups. Each drug was given to the animals intravenously. The dosing frequency was once a week (qw), qw 2 or qw 3.DP303c induced obvious tumor growth inhibition at a single dose of 1 mg/kg.
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In Vitro Model | Breast adenocarcinoma | SK-BR-3 cells | CVCL_0033 | ||
Experiment 9 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 83.94% (Day 18) | High HER2 expression (HER2+++/++) | ||
Method Description |
DP303c (3 mg/kg).
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In Vivo Model | SK-OV-3 cell line xenograft model | ||||
In Vitro Model | Ovarian serous cystadenocarcinoma | SK-OV-3 cells | CVCL_0532 | ||
Experiment 10 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 90.48% (Day 21) | High HER2 expression (HER2+++/++) | ||
Method Description |
DP001 (15 mg/kg).
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In Vivo Model | HCC1954 cell line xenograft model | ||||
In Vitro Model | Breast ductal carcinoma | HCC1954 cells | CVCL_1259 | ||
Experiment 11 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 91.60% (Day 25) | High HER2 expression (HER2+++/++) | ||
Method Description |
T-DM1 (10 mg/kg).
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In Vivo Model | NCI-N87 xenograft model | ||||
In Vitro Model | Gastric tubular adenocarcinoma | NCI-N87 cells | CVCL_1603 | ||
Experiment 12 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 94.00% (Day 25) | High HER2 expression (HER2+++/++) | ||
Method Description |
DP303c (10 mg/kg).
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In Vivo Model | NCI-N87 xenograft model | ||||
In Vitro Model | Gastric tubular adenocarcinoma | NCI-N87 cells | CVCL_1603 | ||
Experiment 13 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 94.00% (Day 25) | High HER2 expression (HER2+++/++) | ||
Method Description |
DP303c (2.5 mg/kg).
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In Vivo Model | NCI-N87 xenograft model | ||||
In Vitro Model | Gastric tubular adenocarcinoma | NCI-N87 cells | CVCL_1603 | ||
Experiment 14 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 94.00% (Day 25) | High HER2 expression (HER2+++/++) | ||
Method Description |
DP303c (5 mg/kg).
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In Vivo Model | NCI-N87 xenograft model | ||||
In Vitro Model | Gastric tubular adenocarcinoma | NCI-N87 cells | CVCL_1603 | ||
Experiment 15 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 94.10% (Day 18) | High HER2 expression (HER2+++) | ||
Method Description |
Pathogen-free female nude mice were injected subcutaneously with each cell suspension. According to tumor volumes,the mice were randomly divided in two groups: treatment and control groups. Each drug was given to the animals intravenously. The dosing frequency was once a week (qw), qw 2 or qw 3.DP303c induced obvious tumor growth inhibition at a single dose of 3 mg/kg.
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In Vitro Model | Breast adenocarcinoma | SK-BR-3 cells | CVCL_0033 | ||
Experiment 16 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 94.16% (Day 18) | High HER2 expression (HER2+++/++) | ||
Method Description |
T-DM1 (10 mg/kg).
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In Vivo Model | SK-OV-3 cell line xenograft model | ||||
In Vitro Model | Ovarian serous cystadenocarcinoma | SK-OV-3 cells | CVCL_0532 | ||
Experiment 17 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 94.30% (Day 21) | High HER2 expression (HER2+++/++) | ||
Method Description |
T-DM1 (15 mg/kg).
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In Vivo Model | HCC1954 cell line xenograft model | ||||
In Vitro Model | Breast ductal carcinoma | HCC1954 cells | CVCL_1259 | ||
Experiment 18 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 97.00% (Day 21) | High HER2 expression (HER2+++/++) | ||
Method Description |
DP303c (10 mg/kg).
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In Vivo Model | HCC1954 cell line xenograft model | ||||
In Vitro Model | Breast ductal carcinoma | HCC1954 cells | CVCL_1259 | ||
Experiment 19 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 97.00% (Day 21) | High HER2 expression (HER2+++/++) | ||
Method Description |
DP303c (15 mg/kg).
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In Vivo Model | HCC1954 cell line xenograft model | ||||
In Vitro Model | Breast ductal carcinoma | HCC1954 cells | CVCL_1259 | ||
Experiment 20 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 97.00% (Day 21) | High HER2 expression (HER2+++/++) | ||
Method Description |
DP303c (3 mg/kg).
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In Vivo Model | HCC1954 cell line xenograft model | ||||
In Vitro Model | Breast ductal carcinoma | HCC1954 cells | CVCL_1259 | ||
Experiment 21 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 97.10% (Day 25) | High HER2 expression (HER2+++) | ||
Method Description |
Pathogen-free female nude mice were injected subcutaneously with each cell suspension. According to tumor volumes,the mice were randomly divided in two groups: treatment and control groups. Each drug was given to the animals intravenously. The dosing frequency was once a week (qw), qw 2 or qw 3.DP303c induced obvious tumor growth inhibition at a single dose of 3 mg/kg.
Click to Show/Hide
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In Vitro Model | Breast ductal carcinoma | HCC1954 cells | CVCL_1259 | ||
Experiment 22 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 97.50% (Day 25) | High HER2 expression (HER2+++) | ||
Method Description |
Pathogen-free female nude mice were injected subcutaneously with each cell suspension. According to tumor volumes,the mice were randomly divided in two groups: treatment and control groups. Each drug was given to the animals intravenously. The dosing frequency was once a week (qw), qw 2 or qw 3.DP303c induced obvious tumor growth inhibition at a single dose of 2.5 mg/kg.
Click to Show/Hide
|
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In Vitro Model | Gastric tubular adenocarcinoma | NCI-N87 cells | CVCL_1603 | ||
Experiment 23 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 97.50% (Day 25) | High HER2 expression (HER2+++) | ||
Method Description |
Pathogen-free female nude mice were injected subcutaneously with each cell suspension. According to tumor volumes,the mice were randomly divided in two groups: treatment and control groups. Each drug was given to the animals intravenously. The dosing frequency was once a week (qw), qw 2 or qw 3.DP303c induced obvious tumor growth inhibition at a single dose of 10 mg/kg.
Click to Show/Hide
|
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In Vitro Model | Breast ductal carcinoma | HCC1954 cells | CVCL_1259 | ||
Experiment 24 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 97.80% (Day 25) | High HER2 expression (HER2+++) | ||
Method Description |
Pathogen-free female nude mice were injected subcutaneously with each cell suspension. According to tumor volumes,the mice were randomly divided in two groups: treatment and control groups. Each drug was given to the animals intravenously. The dosing frequency was once a week (qw), qw 2 or qw 3.DP303c induced obvious tumor growth inhibition at a single dose of 5 mg/kg.
Click to Show/Hide
|
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In Vitro Model | Gastric tubular adenocarcinoma | NCI-N87 cells | CVCL_1603 | ||
Experiment 25 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 97.80% (Day 18) | High HER2 expression (HER2+++) | ||
Method Description |
Pathogen-free female nude mice were injected subcutaneously with each cell suspension. According to tumor volumes,the mice were randomly divided in two groups: treatment and control groups. Each drug was given to the animals intravenously. The dosing frequency was once a week (qw), qw 2 or qw 3.DP303c induced obvious tumor growth inhibition at a single dose of 10 mg/kg.
Click to Show/Hide
|
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In Vitro Model | Breast adenocarcinoma | SK-BR-3 cells | CVCL_0033 | ||
Experiment 26 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 97.80% (Day 32) | Moderate HER2 expression (HER2++) | ||
Method Description |
Pathogen-free female nude mice were injected subcutaneously with each cell suspension. According to tumor volumes,the mice were randomly divided in two groups: treatment and control groups. Each drug was given to the animals intravenously. The dosing frequency was once a week (qw), qw 2 or qw 3.DP303c induced obvious tumor growth inhibition at a single dose of 1 mg/kg.
Click to Show/Hide
|
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In Vitro Model | Breast ductal carcinoma | JIMT-1 cells | CVCL_2077 | ||
Experiment 27 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 98.50% (Day 25) | High HER2 expression (HER2+++) | ||
Method Description |
Pathogen-free female nude mice were injected subcutaneously with each cell suspension. According to tumor volumes,the mice were randomly divided in two groups: treatment and control groups. Each drug was given to the animals intravenously. The dosing frequency was once a week (qw), qw 2 or qw 3.DP303c induced obvious tumor growth inhibition at a single dose of 10 mg/kg.
Click to Show/Hide
|
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In Vitro Model | Gastric tubular adenocarcinoma | NCI-N87 cells | CVCL_1603 | ||
Experiment 28 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 98.54% (Day 18) | High HER2 expression (HER2+++/++) | ||
Method Description |
DP303c (10 mg/kg).
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In Vivo Model | SK-OV-3 cell line xenograft model | ||||
In Vitro Model | Ovarian serous cystadenocarcinoma | SK-OV-3 cells | CVCL_0532 | ||
Experiment 29 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 98.80% (Day 32) | Moderate HER2 expression (HER2++) | ||
Method Description |
Pathogen-free female nude mice were injected subcutaneously with each cell suspension. According to tumor volumes,the mice were randomly divided in two groups: treatment and control groups. Each drug was given to the animals intravenously. The dosing frequency was once a week (qw), qw 2 or qw 3.DP303c induced obvious tumor growth inhibition at a single dose of 3 mg/kg.
Click to Show/Hide
|
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In Vitro Model | Breast ductal carcinoma | JIMT-1 cells | CVCL_2077 | ||
Experiment 30 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 99.10% (Day 25) | High HER2 expression (HER2+++) | ||
Method Description |
Pathogen-free female nude mice were injected subcutaneously with each cell suspension. According to tumor volumes,the mice were randomly divided in two groups: treatment and control groups. Each drug was given to the animals intravenously. The dosing frequency was once a week (qw), qw 2 or qw 3.DP303c induced obvious tumor growth inhibition at a single dose of 15 mg/kg.
Click to Show/Hide
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In Vitro Model | Breast ductal carcinoma | HCC1954 cells | CVCL_1259 | ||
Experiment 31 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 99.90% (Day 32) | Moderate HER2 expression (HER2++) | ||
Method Description |
Pathogen-free female nude mice were injected subcutaneously with each cell suspension. According to tumor volumes,the mice were randomly divided in two groups: treatment and control groups. Each drug was given to the animals intravenously. The dosing frequency was once a week (qw), qw 2 or qw 3.DP303c induced obvious tumor growth inhibition at a single dose of 10 mg/kg.
Click to Show/Hide
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In Vitro Model | Breast ductal carcinoma | JIMT-1 cells | CVCL_2077 | ||
Experiment 32 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 100.00% (Day 32) | Moderate HER2 expression (HER2++) | ||
Method Description |
DP303c (1 mg/kg).
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In Vivo Model | JIMT -1 cell line xenograft model | ||||
In Vitro Model | Breast ductal carcinoma | JIMT-1 cells | CVCL_2077 | ||
Experiment 33 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 100.00% (Day 32) | Moderate HER2 expression (HER2++) | ||
Method Description |
DP303c (10 mg/kg).
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In Vivo Model | JIMT -1 cell line xenograft model | ||||
In Vitro Model | Breast ductal carcinoma | JIMT-1 cells | CVCL_2077 | ||
Experiment 34 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 100.00% (Day 32) | Moderate HER2 expression (HER2++) | ||
Method Description |
DP303c (3 mg/kg).
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In Vivo Model | JIMT -1 cell line xenograft model | ||||
In Vitro Model | Breast ductal carcinoma | JIMT-1 cells | CVCL_2077 |
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) |
0.07 nM
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Moderate HER2 expression (HER2++; HER2 MFI=157,231) | ||
Method Description |
Comparison of in vitro Activity Between DP303c and T -DM1 in Variable HER2 Cell Lines.
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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 (IC50) |
0.07 nM
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High HER2 expression (HER2+++) | ||
Method Description |
To obtain a single-cell suspension, the cells were harvested and resuspended. The cell density was adjusted to 1 x105 cells/mL and seeded in a 96-well cell culture plate at 100 uL/well (1 x104 cells/well). DP303c labeled with DyLight 488 was added into the 96-well plate with a final concentration of 2 ug/mL.
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In Vitro Model | Breast adenocarcinoma | SK-BR-3 cells | CVCL_0033 | ||
Experiment 3 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) |
0.08 nM
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High HER2 expression (HER2+++; HER2 MFI=987,353) | ||
Method Description |
Comparison of in vitro Activity Between DP303c and T -DM1 in Variable HER2 Cell Lines.
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In Vitro Model | Invasive breast carcinoma | BT-474 cells | CVCL_0179 | ||
Experiment 4 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) |
0.08 nM
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Negative HER2 expression (HER2-; HER2 MFI=256) | ||
Method Description |
To obtain a single-cell suspension, the cells were harvested and resuspended. The cell density was adjusted to 1x105 cells/mL and seeded in a 96-well cell culture plate at 100 uL/well (1 x104 cells/well). DP303c labeled with DyLight 488 was added into the 96-well plate with a final concentration of 2 ug/mL.
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In Vitro Model | Invasive breast carcinoma | BT-474 cells | CVCL_0179 | ||
Experiment 5 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) |
0.15 nM
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High HER2 expression (HER2+++) | ||
Method Description |
Comparison of in vitro Activity Between DP303c and T -DM1 in Variable HER2 Cell Lines.
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In Vitro Model | Breast ductal carcinoma | HCC1954 cells | CVCL_1259 | ||
Experiment 6 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) |
0.15 nM
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High HER2 expression (HER2+++) | ||
Method Description |
To obtain a single-cell suspension, the cells were harvested and resuspended. The cell density was adjusted to 1 x105 cells/mL and seeded in a 96-well cell culture plate at 100 uL/well (1 x104 cells/well). DP303c labeled with DyLight 488 was added into the 96-well plate with a final concentration of 2 ug/mL.
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In Vitro Model | Breast ductal carcinoma | HCC1954 cells | CVCL_1259 | ||
Experiment 7 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) |
0.22 nM
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Negative HER2 expression (HER2-) | ||
Method Description |
Comparison of in vitro Activity Between DP303c and T -DM1 in Variable HER2 Cell Lines.
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In Vitro Model | Ovarian serous cystadenocarcinoma | SK-OV-3 cells | CVCL_0532 | ||
Experiment 8 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) |
0.22 nM
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High HER2 expression (HER2+++) | ||
Method Description |
To obtain a single-cell suspension, the cells were harvested and resuspended. The cell density was adjusted to 1 x105 cells/mL and seeded in a 96-well cell culture plate at 100 uL/well (1 x104 cells/well). DP303c labeled with DyLight 488 was added into the 96-well plate with a final concentration of 2 ug/mL.
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In Vitro Model | Ovarian serous cystadenocarcinoma | SK-OV-3 cells | CVCL_0532 | ||
Experiment 9 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) |
0.23 nM
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High HER2 expression (HER2+++; HER2 MFI=804,573) | ||
Method Description |
Comparison of in vitro Activity Between DP303c and T -DM1 in Variable HER2 Cell Lines.
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In Vitro Model | Gastric tubular adenocarcinoma | NCI-N87 cells | CVCL_1603 | ||
Experiment 10 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) |
0.23 nM
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High HER2 expression (HER2+++; HER2 MFI=892,333) | ||
Method Description |
To obtain a single-cell suspension, the cells were harvested and resuspended. The cell density was adjusted to 1 x105 cells/mL and seeded in a 96-well cell culture plate at 100 uL/well (1 x104 cells/well). DP303c labeled with DyLight 488 was added into the 96-well plate with a final concentration of 2 ug/mL.
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In Vitro Model | Gastric tubular adenocarcinoma | NCI-N87 cells | CVCL_1603 | ||
Experiment 11 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) |
3.39 nM
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High HER2 expression (HER2+++) | ||
Method Description |
Comparison of in vitro Activity Between DP303c and T -DM1 in Variable HER2 Cell Lines.
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In Vitro Model | Breast ductal carcinoma | JIMT-1 cells | CVCL_2077 | ||
Experiment 12 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) |
3.39 nM
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Moderate HER2 expression (HER2++) | ||
Method Description |
To obtain a single-cell suspension, the cells were harvested and resuspended. The cell density was adjusted to 1x105 cells/mL and seeded in a 96-well cell culture plate at 100 uL/well (1x104 cells/well). DP303c labeled with DyLight 488 was added into the 96-well plate with a final concentration of 2 ug/mL.
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In Vitro Model | Breast ductal carcinoma | JIMT-1 cells | CVCL_2077 | ||
Experiment 13 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) | > 50.00 nM | High HER2 expression (HER2+++; HER2 MFI=1,106,494) | ||
Method Description |
To obtain a single-cell suspension, the cells were harvested and resuspended. The cell density was adjusted to 1x105 cells/mL and seeded in a 96-well cell culture plate at 100 uL/well (1x104 cells/well). DP303c labeled with DyLight 488 was added into the 96-well plate with a final concentration of 2 ug/mL.
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In Vitro Model | Breast adenocarcinoma | MDA-MB-468 cells | CVCL_0419 | ||
Experiment 14 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) | > 1000.00 nM | High HER2 expression (HER2+++; HER2 MFI=765,629) | ||
Method Description |
Comparison of in vitro Activity Between DP303c and T -DM1 in Variable HER2 Cell Lines.
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In Vitro Model | Breast adenocarcinoma | MDA-MB-468 cells | CVCL_0419 |
References
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