Antibody-drug Conjugate Information
General Information of This Antibody-drug Conjugate (ADC)
ADC ID |
DRG0LGQVY
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ADC Name |
HuFR1-57-SMCC-DM1
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Drug Status |
Investigative
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Indication |
In total 4 Indication(s)
Cervical cancer [ICD11:2C77]
Investigative
Gestational choriocarcinoma [ICD11:2C75]
Investigative
Lung cancer [ICD11:2C25]
Investigative
Ovarian cancer [ICD11:2C73]
Investigative
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Drug-to-Antibody Ratio |
3.3
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Structure | ||||||
Antibody Name |
Anti-FOLR1 huFR1-57
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Antibody Info | ||||
Antigen Name |
Folate receptor alpha (FOLR1)
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Antigen Info | ||||
Payload Name |
Mertansine DM1
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Payload Info | ||||
Therapeutic Target |
Microtubule (MT)
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Target Info | ||||
Linker Name |
Succinimidyl-4-(N-maleimidomethyl)cyclohexane-1-carboxylate (SMCC)
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Linker Info | ||||
Conjugate Type |
Random conjugation through nucleophilic lysines.
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Combination Type |
Emtansine
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General Information of The Activity Data Related to This ADC
Discovered Using Cell Line-derived Xenograft Model
Standard Type | Value | Units | Cell Line | Disease Model |
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Tumor Growth Inhibition value (TGI) |
86.67
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%
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KB cells
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Human papillomavirus-related endocervical adenocarcinoma
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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) |
0.15±0.02
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nM
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KB cells
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Human papillomavirus-related endocervical adenocarcinoma
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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) | 86.67% (Day 12) | High FOLR1 expression (FOLR1+++; 4,500,000 FOLR1 molecules/cell) | ||
Method Description |
Five-week-old female CB-17 severe combined immunodeficient (SCID) mice were obtained and quarantined for 7 days prior to study initiation Mice were inoculated subcutaneously with KB cells (1 x107 cells per mouse) resuspended in serum-free culture mediaMice with established KB xenografts were dosed with a single intravenous injection of 200 g of conjugated maytansinoid per kg, equivalent to 102 mg/kg antibody on day 6 after cell inoculationTumor dimensions were measured twice weekly and volume was calculated as (A B2) 05, where A represents the largest and B the perpendicular tumor diameter.
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In Vivo Model | FRalpha-positive KB CDX model | ||||
In Vitro Model | Human papillomavirus-related endocervical adenocarcinoma | KB cells | CVCL_0372 |
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) | 0.15±0.02 nM | High FOLR1 expression (FOLR1+++; 4,500,000 FOLR1 molecules/cell) | ||
Method Description |
Dilutions of conjugates or unconjugated maytansinoid in the appropriate culture medium were added to wells of 96-well flat-bottomed plates containing 1 x103 cells per well The plates were incubated at 37°C, 6% CO2 for either 5 days (continuos exposure) or for 4 hours followed by 5-day incubation in conjugate-free medium (short exposure). Cell viability was determined by the WST-8 assay in accordance with the manufacturer's protocol, and IC50 were generated using a sigmoidal dose-response (variable slope) nonlinear regression curve fit.
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In Vitro Model | Human papillomavirus-related endocervical adenocarcinoma | KB cells | CVCL_0372 |
References
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