General Information of This Antibody-drug Conjugate (ADC)
ADC ID
DRG0QYKCV
ADC Name
TWEAKR ADC 3d
Synonyms
TWEAKR-ADC-3d
   Click to Show/Hide
Drug Status
Investigative
Indication
In total 4 Indication(s)
Bladder cancer [ICD11:2C94]
Investigative
Colon cancer [ICD11:2B90]
Investigative
Lung mucoepidermoid carcinoma [ICD11:2C25]
Investigative
Pancreatic ductal adenocarcinoma [ICD11:2C10]
Investigative
Drug-to-Antibody Ratio
2.2
Antibody Name
BAY-356
 Antibody Info 
Antigen Name
Tumor necrosis factor receptor superfamily member 12A (TNFRSF12A)
 Antigen Info 
Payload Name
Kinesin spindle protein (KSP) inhibitor 3d
 Payload Info 
Therapeutic Target
Kinesin-like protein KIF11 (KIF11)
 Target Info 
Linker Name
Open-chain glycine maleimide
 Linker Info 
Conjugate Type
Random conjugation through reduced inter-chain cysteines.
General Information of The Activity Data Related to This ADC
Revealed Based on the Cell Line Data
Click To Hide/Show 3 Activity Data Related to This Level
Standard Type Value Units Cell Line Disease Model
Half Maximal Inhibitory Concentration (IC50) 
600
nM
NCI-H292 cells
Lung mucoepidermoid carcinoma
Half Maximal Inhibitory Concentration (IC50) 
600
nM
BxPC-3 cells
Pancreatic ductal adenocarcinoma
Half Maximal Inhibitory Concentration (IC50) 
600
nM
LoVo cells
Colon adenocarcinoma
Full List of Activity Data of This Antibody-drug Conjugate
Revealed Based on the Cell Line Data
Click To Hide/Show 3 Activity Data Related to This Level
Experiment 1 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal Inhibitory Concentration (IC50) 600 nM Positive TNFRSF12A expression (TNFRSF12A +++/++)
Method Description
Cytotoxicity of ADCs, SMOL KSP inhibitors, and payload metabolite were determined in TWEAKR-positive cancer cell lines 72 h after treatment with the Promega CellTiter Glo (CTG) cell viability assay according to manufacturers instructions.
In Vitro Model Lung mucoepidermoid carcinoma NCI-H292 cells CVCL_0455
Experiment 2 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal Inhibitory Concentration (IC50) 600 nM Positive TNFRSF12A expression (TNFRSF12A +++/++)
Method Description
Cytotoxicity of ADCs, SMOL KSP inhibitors, and payload metabolite were determined in TWEAKR-positive cancer cell lines 72 h after treatment with the Promega CellTiter Glo (CTG) cell viability assay according to manufacturers instructions.
In Vitro Model Pancreatic ductal adenocarcinoma BxPC-3 cells CVCL_0186
Experiment 3 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal Inhibitory Concentration (IC50) 600 nM Positive TNFRSF12A expression (TNFRSF12A +++/++)
Method Description
Cytotoxicity of ADCs, SMOL KSP inhibitors, and payload metabolite were determined in TWEAKR-positive cancer cell lines 72 h after treatment with the Promega CellTiter Glo (CTG) cell viability assay according to manufacturers instructions.
In Vitro Model Colon adenocarcinoma LoVo cells CVCL_0399
References
Ref 1 Antibody-Prodrug Conjugates with KSP Inhibitors and Legumain-Mediated Metabolite Formation. Chemistry. 2019 Jun 21;25(35):8208-8213. doi: 10.1002/chem.201900441. Epub 2019 Apr 15.

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