Antibody-drug Conjugate Information
General Information of This Antibody-drug Conjugate (ADC)
ADC ID |
DRG0GTUOW
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ADC Name |
HuM25-mcMMAF-E2
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Synonyms |
HuM25 mcMMAF-E2; huM25 mcMMAF-E2
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Organization |
AbbVie, Inc.
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Drug Status |
Investigative
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Indication |
In total 3 Indication(s)
Colon cancer [ICD11:2B90]
Investigative
Non-small cell lung cancer [ICD11:2C25]
Investigative
Pancreatic cancer [ICD11:2C10]
Investigative
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Drug-to-Antibody Ratio |
2
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Structure | ||||||
Antibody Name |
HuM25
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Antibody Info | ||||
Antigen Name |
Leucine-rich repeat-containing protein 15 (LRRC15)
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Antigen Info | ||||
Payload Name |
Monomethyl auristatin F
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Payload Info | ||||
Therapeutic Target |
Microtubule (MT)
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Target Info | ||||
Linker Name |
Maleimido-caproyl
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Linker Info | ||||
Conjugate Type |
Random conjugation through reduced inter-chain cysteines.
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Combination Type |
McMMAF
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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 Inhibitory Concentration (IC50) |
0.01 - 0.10
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nM
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HCT 116 cells
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Colon 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) | 0.00% | Positive LRRC15 expression (LRRC15 +++/++) | ||
Method Description |
LRRC15 expression on stromal cells asassessed by IHC in an untreated xenograft tumor of 200-800 mm in volume, representative for eachxenograft model. In vivo activity of huM25-MCMMAF-E2 (12 mg/kg) was demonstrated in PANC-1 xenografts.
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In Vivo Model | PANC-1 CDX model | ||||
In Vitro Model | Pancreatic ductal adenocarcinoma | PANC-1 cells | CVCL_0480 | ||
Experiment 2 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | 8.47% (Day 11) | High LRRC15 expression (LRRC15+++; IHC 3+) | ||
Method Description |
LRRC15 expression on stromal cells asassessed by IHC in an untreated xenograft tumor of 200-800 mm in volume, representative for eachxenograft model. In vivo activity of huM25-MCMMAF-E2 (6 mg/kg) was demonstrated in EBC-1 xenografts.
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In Vivo Model | EBC-1 CDX model | ||||
In Vitro Model | Lung squamous cell carcinoma | EBC-1 cells | CVCL_2891 |
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Half Maximal Inhibitory Concentration (IC50) | 0.01 nM - 0.10 nM | Positive LRRC15 expression (LRRC15 +++/++) | ||
Method Description |
Cancer cell lines were incubated with compounds for 72 h. IC50 values were determined by quantitating viable cells using a CellTiter-Glo luminescent assay.
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In Vitro Model | Colon carcinoma | HCT 116 cells | CVCL_0291 |
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