General Information of This Antibody-drug Conjugate (ADC)
ADC ID
DRG0EZXOL
ADC Name
TWEAKR-KSP-ADC 1.3
Synonyms
TWEAKR-KSP-ADC-1.3
   Click to Show/Hide
Drug Status
Investigative
Indication
In total 3 Indication(s)
Colorectal cancer [ICD11:2B91]
Investigative
Non-small cell lung cancer [ICD11:2C25]
Investigative
Pancreatic cancer [ICD11:2C10]
Investigative
Drug-to-Antibody Ratio
3.5
Antibody Name
Anti-TWEAKR mAb
 Antibody Info 
Antigen Name
Tumor necrosis factor receptor superfamily member 12A (TNFRSF12A)
 Antigen Info 
Payload Name
Pyrrole based kinesin spindle protein inhibitor
 Payload Info 
Therapeutic Target
Kinesin-like protein KIF11 (KIF11)
 Target Info 
Linker Name
Kinesin spindle protein inhibitor (KSPi)-ADC linker 3
 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) 
0.09
nM
LoVo cells
Colon adenocarcinoma
Half Maximal Inhibitory Concentration (IC50) 
0.74
nM
NCI-H292 cells
Lung mucoepidermoid carcinoma
Half Maximal Inhibitory Concentration (IC50) 
0.87
nM
BxPC-3 cells
Pancreatic ductal 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) 0.09 nM High TWEAKR expression (TWEAKR +++)
Method Description
In vitro potency of SMOL KSPi compound A and of TWEAKR-KSPiADCs 1.1., 1.2, 1.3, 1.4, 2.1, and 2.2 in TWEAKR-expressing cell lines versus selected respective isotype control ADCs 1.4 and 2.2 with same linker payload chemistry.
In Vitro Model Colon adenocarcinoma LoVo cells CVCL_0399
Experiment 2 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal Inhibitory Concentration (IC50) 0.74 nM High TWEAKR expression (TWEAKR +++)
Method Description
In vitro potency of SMOL KSPi compound A and of TWEAKR-KSPiADCs 1.1., 1.2, 1.3, 1.4, 2.1, and 2.2 in TWEAKR-expressing cell lines versus selected respective isotype control ADCs 1.4 and 2.2 with same linker payload chemistry.
In Vitro Model Lung mucoepidermoid carcinoma NCI-H292 cells CVCL_0455
Experiment 3 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal Inhibitory Concentration (IC50) 0.87 nM High TWEAKR expression (TWEAKR +++)
Method Description
In vitro potency of SMOL KSPi compound A and of TWEAKR-KSPiADCs 1.1., 1.2, 1.3, 1.4, 2.1, and 2.2 in TWEAKR-expressing cell lines versus selected respective isotype control ADCs 1.4 and 2.2 with same linker payload chemistry.
In Vitro Model Pancreatic ductal adenocarcinoma BxPC-3 cells CVCL_0186
References
Ref 1 Antibody-Drug Conjugates with Pyrrole-Based KSP Inhibitors as the Payload Class. Angew Chem Int Ed Engl. 2018 Nov 12;57(46):15243-15247. doi: 10.1002/anie.201807619. Epub 2018 Oct 15.

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