General Information of This Antibody-drug Conjugate (ADC)
ADC ID
DRG0KXPLC
ADC Name
hmAbH11L11-Dxd
Synonyms
hmAbH11L11-Dxd
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Organization
DAIICHI SAMKO COMPANY, LIMITED
Drug Status
Investigative
Drug-to-Antibody Ratio
7.5
Structure
Antibody Name
hmAb-L11
 Antibody Info 
Antigen Name
Leukocyte antigen CD37 (CD37)
 Antigen Info 
Payload Name
Undisclosed
Therapeutic Target
Stimulator of interferon genes protein (STING1)
 Target Info 
Linker Name
Succinimidyl-4- (N-maleimidomethyl)cyclohexane-1-carboxylate (SMCC)
 Linker Info 
Conjugate Type
Random conjugation through reduced inter-chain cysteines.
Combination Type
N-[6- (2,5-dioxo-2,5-dihydro-1h-pyrrol-1-yl) hexanoyl]glycylglycyl-phenylalanyl-n-[ (2-{[ (1s,9s)-9-ethyl-5-fluoro-9-hydroxy-4-methyl-10,13-dioxo-2,3,9,10,13,15-hexahydro-1h,12h-benzo[de]pyrano[3',4':6,7]indolizino[1,2-b]quinolin-1-yl]amino}-2-oxoethoxy)methyl]glycinamide
ADC-specific functional property(2027 Update)
Binding Affinity
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Dissocation Constant (Kd) Binding Target Description Reference
2000-2500 .
CD37
The binding activity was evaluated by flow cytometry on CD37-positive human diffuse large B-cell lymphoma cell line OCI-LY7 (DSMZ), the cells were suspended by the addition of each of the four antibody-drug conjugates or anegative control antibody-drug conjugate (hmAb-IgG1-DXd) produced using human IgG at each concentration, the MFI of antibody-drug conjugates at 100 ug/mL was measured.

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[1]
Circulating Stability
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Incubation Time 5hr Release 79.7% Reference
[1]
Incubation Medium Each anti-CD37 humanized antibody-diug conjugate dissolved at 20 mg/mL in ABS was diluted into 2 mg/mL with Otsuka physiological saline and left standing atroom temperature or 4°C. for 5 hours, the recovery rate of the anti-CD37 humanized antibody-drug conjugate was calculated.
Description
Evaluation of Recovery Rate of Anti-CD37 Humanized Antibody-Drug Conjugate into Physiological Saline.
General Information of The Activity Data Related to This ADC
Discovered Using Cell Line-derived Xenograft Model
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Standard Type Value Units Cell Line Disease Model
Tumor Growth lnhibition value (TGl) 
< 30
%
Undisclosed Undisclosed
Tumor Growth lnhibition value (TGl) 
> 50
%
Undisclosed Undisclosed
Tumor Growth lnhibition value (TGl) 
> 50
%
Undisclosed Undisclosed
Tumor Growth lnhibition value (TGl) 
> 90
%
Undisclosed Undisclosed
Tumor Growth lnhibition value (TGl) 
> 100
%
Undisclosed Undisclosed
Tumor Growth lnhibition value (TGl) 
> 100
%
Undisclosed Undisclosed
Revealed Based on the Cell Line Data
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Standard Type Value Units Cell Line Disease Model
Half Maximal inhibitory Concentration (lC50) 
≈ 1
nM
CVCL_1881
Diffuse large B-cell lymphoma germinal center B-cell type, Diffuse large B-cell lymphoma
Full List of Activity Data of This Antibody-drug Conjugate
Discovered Using Cell Line-derived Xenograft Model
Click To Hide/Show 6 Activity Data Related to This Level
Experiment 1 Reporting the Activity Date of This ADC [1]
Efficacy Data Tumor Growth lnhibition value (TGl) < 30% Positive CD37 expression (CD37+++/++)
Method Description
CD37-positive human diffuse large B-cell lymphoma cell line SU-DHL-8 (ATCC) was subcutaneously inoculated at a dose of 5x106 cells to the right flank region of each five or six-week-old female SCID mouse (Day 0). On Day 7, the mice were randomly grouped. On the day of grouping, the antibodydrug conjugates hmAb-H11L11-DXd was intravenously administered at a dose of 1 mg/kg to the tail of each mouse. An antibody-drug conjugate (hmAb-IgG1-DXd) produced using human IgG was administered as a negative control at a dose of 3 mg/kg in the same manner as above. The long diameter and short diameter of the inoculated tumor were measured twice a week using electronic digital calipers, and the volume of the tumor was then calculated.

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In Vivo Model SU-DHL-8 (ATCC) female SCID mouse model
Experiment 2 Reporting the Activity Date of This ADC [1]
Efficacy Data Tumor Growth lnhibition value (TGl) > 50% Positive CD37 expression (CD37+++/++)
Method Description
CD37-positive human diffuse large B-cell lymphoma cell line OCI-LY7 (DSMZ) was subcutaneously inoculated at a dose of 1x107 cells to the right flank region of each five or six-week-old female SCID mouse (Day 0). On Day 9, the mice were randomly grouped. On the day of grouping, the antibodydrug conjugates hmAb-H11L11-DXd was intravenously administered at a dose of 1 mg/kg to the tail of each mouse. An antibody-drug conjugate (hmAb-IgG1-DXd) produced using human IgG was administered as a negative control at a dose of 3 mg/kg in the same manner as above. The long diameter and short diameter of the inoculated tumor were measured twice a week using electronic digital calipers, and the volume of the tumor was then calculated.

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In Vivo Model OCI-LY7 (DSMZ) female SCID mouse model
Experiment 3 Reporting the Activity Date of This ADC [1]
Efficacy Data Tumor Growth lnhibition value (TGl) > 50% Positive CD37 expression (CD37+++/++)
Method Description
CD37-positive human diffuse large B-cell lymphoma cell line WSU-DLCL2 (DSMZ) was subcutaneously inoculated at a dose of 1x107 cells to the right flank region of each five or six-week-old female SCID mouse (Day 0). On Day 11, the mice were randomly grouped. On the day of grouping, the antibodydrug conjugates hmAb-H11L11-DXd was intravenously administered at a dose of 1 mg/kg to the tail of each mouse. An antibody-drug conjugate (hmAb-IgG1-DXd) produced using human IgG was administered as a negative control at a dose of 3 mg/kg in the same manner as above. The long diameter and short diameter of the inoculated tumor were measured twice a week using electronic digital calipers, and the volume of the tumor was then calculated.

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In Vivo Model WSU-DLCL2 (DSMZ) female SCID mouse model
Experiment 4 Reporting the Activity Date of This ADC [1]
Efficacy Data Tumor Growth lnhibition value (TGl) > 90% Positive CD37 expression (CD37+++/++)
Method Description
CD37-positive human diffuse large B-cell lymphoma cell line WSU-DLCL2 (DSMZ) was subcutaneously inoculated at a dose of 1x107 cells to the right flank region of each five or six-week-old female SCID mouse (Day 0). On Day 11, the mice were randomly grouped. On the day of grouping, the antibodydrug conjugates hmAb-H11L11-DXd was intravenously administered at a dose of 1 mg/kg to the tail of each mouse. An antibody-drug conjugate (hmAb-IgG1-DXd) produced using human IgG was administered as a negative control at a dose of 3 mg/kg in the same manner as above. The long diameter and short diameter of the inoculated tumor were measured twice a week using electronic digital calipers, and the volume of the tumor was then calculated.

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In Vivo Model WSU-DLCL2 (DSMZ) female SCID mouse model
Experiment 5 Reporting the Activity Date of This ADC [1]
Efficacy Data Tumor Growth lnhibition value (TGl) > 100% Positive CD37 expression (CD37+++/++)
Method Description
CD37-positive human diffuse large B-cell lymphoma cell line OCI-LY7 (DSMZ) was subcutaneously inoculated at a dose of 1x107 cells to the right flank region of each five or six-week-old female SCID mouse (Day 0). On Day 9, the mice were randomly grouped. On the day of grouping, the antibodydrug conjugates hmAb-H11L11-DXd was intravenously administered at a dose of 1 mg/kg to the tail of each mouse. An antibody-drug conjugate (hmAb-IgG1-DXd) produced using human IgG was administered as a negative control at a dose of 3 mg/kg in the same manner as above. The long diameter and short diameter of the inoculated tumor were measured twice a week using electronic digital calipers, and the volume of the tumor was then calculated.

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In Vivo Model OCI-LY7 (DSMZ) female SCID mouse model
Experiment 6 Reporting the Activity Date of This ADC [1]
Efficacy Data Tumor Growth lnhibition value (TGl) > 100% Positive CD37 expression (CD37+++/++)
Method Description
CD37-positive human diffuse large B-cell lymphoma cell line SU-DHL-8 (ATCC) was subcutaneously inoculated at a dose of 5x106 cells to the right flank region of each five or six-week-old female SCID mouse (Day 0). On Day 7, the mice were randomly grouped. On the day of grouping, the antibodydrug conjugates hmAb-H11L11-DXd was intravenously administered at a dose of 1 mg/kg to the tail of each mouse. An antibody-drug conjugate (hmAb-IgG1-DXd) produced using human IgG was administered as a negative control at a dose of 3 mg/kg in the same manner as above. The long diameter and short diameter of the inoculated tumor were measured twice a week using electronic digital calipers, and the volume of the tumor was then calculated.

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In Vivo Model SU-DHL-8 (ATCC) female SCID mouse model
Revealed Based on the Cell Line Data
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Experiment 1 Reporting the Activity Date of This ADC [1]
Efficacy Data Half Maximal inhibitory Concentration (lC50) ≈ 1 nM Positive CD37 expression (CD37+++/++)
Method Description
human diffuse large B-cell lymphoma cell line OCI-LY7 (DSMZ) , 5x10-cells/100 ML/well , IMDM medium , hmnAb-H11L11-DXd was added to the cells such that the final concentrations were from 0.0064 nM to 20 nM. The cells were cultured under conditions of 37°C. and 5% CO2 for 6 days, and thereafter, the number of live cells was measured.
In Vitro Model Diffuse large B-cell lymphoma germinal center B-cell type, Diffuse large B-cell lymphoma OCI-LY7 cells CVCL_1881
References
Ref 1 Anti-CD37 antibody-drug conjugate