General Information of This Antibody-drug Conjugate (ADC)
ADC ID
DRG0FEVOT
ADC Name
HN-02
Synonyms
HN02; HN 02
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Organization
China Pharmaceutical University.; State Key Laboratory of Natural Medicines, Nanjing, China.
Drug Status
Investigative
Drug-to-Antibody Ratio
2
Antibody Name
TG7
 Antibody Info 
Antigen Name
Signal transducer CD24 (CD24)
 Antigen Info 
Payload Name
Undisclosed
Linker Name
Undisclosed
Conjugate Type
Site-specific conjugation-based engineered cysteine sites (CL-V211C)
2027 Update
ADC-specific functional property
Bystander Killing Effect
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Bystander Killing Effect Description Reference
yes
The effect is one of the important factors in the biological activity of ADCs. After treating BEL7402 cells with 1000 nM of HN02 for 1 day, the survival rate of cells decreased from 96.816% to 79.456% when HCT116 cells were treated with the culture supernatant. As time went by, this decrease became more significant. After 2 or 3 days of treatment with 100 nM HN02, the average cell viability dropped to 66.542% and 62.600%, respectively.

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[1]
General Information of The Activity Data Related to This ADC
Discovered Using Cell Line-derived Xenograft Model
Click To Hide/Show 2 Activity Data Related to This Level
Standard Type Value Units Cell Line Disease Model
Tumor Growth lnhibition value (TGl) 
55.288
%
Undisclosed Undisclosed
Tumor Growth lnhibition value (TGl) 
70.25
%
Undisclosed Undisclosed
Full List of Activity Data of This Antibody-drug Conjugate
Discovered Using Cell Line-derived Xenograft Model
Click To Hide/Show 2 Activity Data Related to This Level
Experiment 1 Reporting the Activity Date of This ADC [1]
Efficacy Data Tumor Growth lnhibition value (TGl)
55.29%
Method Description
HN02-L (5 mg/kg): BEL7402 (2×106) cells were injected subcutaneously into the right side of BALB/C nude mice to establish a hepatocellular carcinoma xenograft model. After the mean tumor volume reached 50-100 mm3, the tumor-bearing mice were divided randomly into 5 groups (eight mice/group). TG7 (5 mg/kg), HN02-L (5 mg/kg), HN02-H (10 mg/kg), or saline were injected intravenously every 3 days, and the positive group was treated with the drug sorafenib (20 mg/kg) by gavage daily for 3 w. Body weights and tumor volumes were measured periodically, and tumor volume was calculated using the formula V=LW2 /2 (L: long diameter of the tumor, W: short diameter of the tumor in the vertical direction). All mice were executed on day 21 of treatment, and tumors were excised for subsequent analysis.

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In Vivo Model BEL7402 hepatocellular carcinoma model
Experiment 2 Reporting the Activity Date of This ADC [1]
Efficacy Data Tumor Growth lnhibition value (TGl)
70.25%
Method Description
HN02-H (10 mg/kg): BEL7402 (2×106) cells were injected subcutaneously into the right side of BALB/C nude mice to establish a hepatocellular carcinoma xenograft model. After the mean tumor volume reached 50-100 mm3, the tumor-bearing mice were divided randomly into 5 groups (eight mice/group). TG7 (5 mg/kg), HN02-L (5 mg/kg), HN02-H (10 mg/kg), or saline were injected intravenously every 3 days, and the positive group was treated with the drug sorafenib (20 mg/kg) by gavage daily for 3 w. Body weights and tumor volumes were measured periodically, and tumor volume was calculated using the formula V=LW2 /2 (L: long diameter of the tumor, W: short diameter of the tumor in the vertical direction). All mice were executed on day 21 of treatment, and tumors were excised for subsequent analysis.

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In Vivo Model BEL7402 hepatocellular carcinoma model
References
Ref 1 Site-specific Antibody-Nitric Oxide Conjugate HN02 Possesses Improved Antineoplastic and Safety Properties