Antibody Information
General Information of This Antibody
Antibody ID | ANI0DKNXJ |
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Antibody Name | OBI-888 |
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Antibody Type | Monoclonal antibody (mAb) |
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Antibody Subtype | Humanized IgG |
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Antigen Name | Globo |
Antigen Info | ||||
Click to Show/Hide the Sequence Information of This Antibody | ||||||
Heavy Chain Sequence |
QITLKESGPTLVKPTQTLTLTCTFSGFSLYTFDMGVGWIRQPPGKGLEWLAHIWWDGDKY
YNPALKSRLTISKDTSKNQVVLTMTNMDPVDTATYYCARVRGLHRYYYWFAYWGQGTLVT VSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVL QSSGLYSLSSWTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELL GGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQ YNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSR DELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKS RWQQGNVFSCSVNIHEALHNHYTQKSLSLSPGK Click to Show/Hide
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Light Chain Sequence |
ETVLTQSPATLSLSPGERATLSCRASSSVSYMfHWYQQKPGKSPKPWIYATSNKASGVPS
RFSGSGSGTDFTFTISSLQPEDIATYYCQQWSRRPFTFGQGTKVEIKRTVAAPSVFIFPP SDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLT LSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC Click to Show/Hide
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Each Antibody-drug Conjugate Related to This Antibody
Full Information of The Activity Data of The ADC(s) Related to This Antibody
OBI-999 [Phase 1/2]
Identified from the Human Clinical Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Patients Enrolled |
Advanced solid tumors that had been previously treated with standard-of-care therapy and their physicians had determined that such therapy was no longer effective, or patients had declined to receive further standard-of-care treatments.
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Administration Dosage |
The starting dose of 0.40 mg/kg on day 1 of each 21-day cycle; A standard 3 + 3 dose-escalation design was used, and doses of 0.80, 1.20, and 1.60 mg/kg were also administered on day 1 of each 21-day cycle; intravenous infusion over 60 minutes.
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Related Clinical Trial | |||||
NCT Number | NCT04084366 | Clinical Status | Phase 1 | ||
Clinical Description |
A phase 1/2, open-label, dose-escalation and cohort-expansion study evaluating the safety, pharmacokinetics, and therapeutic activity of OBI-999 in patients with advanced solid tumors.
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Primary Endpoint |
The incidence of dose-limiting toxicities and adverse events and determination of the maximum tolerated dose (MTD)/recommended phase II dose.
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Discovered Using Cell Line-derived Xenograft Model
Experiment 1 Reporting the Activity Date of This ADC | [2] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 34.00% (Day 26) | Positive Globo H expression (Globo H+++/++) | ||
Method Description |
Mice were treated with an intravenous dose of the ADCs at 0.3 mg/kg, qw*6.
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In Vivo Model | MCF-7 CDX model | ||||
In Vitro Model | Invasive breast carcinoma | MCF-7 cells | CVCL_0031 | ||
Experiment 2 Reporting the Activity Date of This ADC | [2] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 60.00% (Day 77) | Positive Globo H expression (Globo H+++/++) | ||
Method Description |
Mice were treated with an intravenous dose of the ADCs at 1 mg/kg, qw*6.
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In Vivo Model | MCF-7 CDX model | ||||
In Vitro Model | Invasive breast carcinoma | MCF-7 cells | CVCL_0031 | ||
Experiment 3 Reporting the Activity Date of This ADC | [2] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 83.00% (Day 53) | Positive Globo H expression (Globo H+++/++) | ||
Method Description |
Mice were treated with an intravenous dose of the ADCs at 1 mg/kg, qw*4.
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In Vivo Model | NCI-N87 CDX model | ||||
In Vitro Model | Gastric tubular adenocarcinoma | NCI-N87 cells | CVCL_1603 | ||
Experiment 4 Reporting the Activity Date of This ADC | [2] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 85.00% (Day 25) | Positive Globo H expression (Globo H+++/++) | ||
Method Description |
Mice were treated with an intravenous dose of the ADCs at 10 mg/kg, qw*4.
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In Vivo Model | NCI-H526 CDX model | ||||
In Vitro Model | Lung small cell carcinoma | NCI-H526 cells | CVCL_1569 | ||
Experiment 5 Reporting the Activity Date of This ADC | [2] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 95.00% (Day 77) | Positive Globo H expression (Globo H+++/++) | ||
Method Description |
Mice were treated with an intravenous dose of the ADCs at 10 mg/kg, qw*2.
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In Vivo Model | MCF-7 CDX model | ||||
In Vitro Model | Invasive breast carcinoma | MCF-7 cells | CVCL_0031 | ||
Experiment 6 Reporting the Activity Date of This ADC | [2] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 97.00% (Day 53) | Positive Globo H expression (Globo H+++/++) | ||
Method Description |
Mice were treated with an intravenous dose of the ADCs at 10 mg/kg, qw*4.
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In Vivo Model | NCI-N87 CDX model | ||||
In Vitro Model | Gastric tubular adenocarcinoma | NCI-N87 cells | CVCL_1603 | ||
Experiment 7 Reporting the Activity Date of This ADC | [2] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 97.00% (Day 53) | Positive Globo H expression (Globo H+++/++) | ||
Method Description |
Mice were treated with an intravenous dose of the ADCs at 1-3 mg/kg, qw*4.
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In Vivo Model | NCI-N87 CDX model | ||||
In Vitro Model | Gastric tubular adenocarcinoma | NCI-N87 cells | CVCL_1603 | ||
Experiment 8 Reporting the Activity Date of This ADC | [2] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 98.00% (Day 77) | Positive Globo H expression (Globo H+++/++) | ||
Method Description |
Mice were treated with an intravenous dose of the ADCs at 3 mg/kg, qw*6.
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In Vivo Model | MCF-7 CDX model | ||||
In Vitro Model | Invasive breast carcinoma | MCF-7 cells | CVCL_0031 | ||
Experiment 9 Reporting the Activity Date of This ADC | [2] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 99.00% (Day 37) | Positive Globo H expression (Globo H+++/++) | ||
Method Description |
Mice were treated with an intravenous dose of the ADCs at 10 mg/kg, qw*4.
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In Vivo Model | HPAC CDX model | ||||
In Vitro Model | Pancreatic adenocarcinoma | HPAC cells | CVCL_3517 |
Revealed Based on the Cell Line Data
Experiment 1 Reporting the Activity Date of This ADC | [3] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 70.70% | |||
Method Description |
In vivo , In each animal study,the antitumor efficacy was evaluated with doses of 1.00, 3.00, or 10.00 mg/kg of OBI-999 via i.v. injection. In NCI-N87 xenograft model,treatment groups of MMAE 0.191 mg/kg and Ctrl-ADC 3 mg/kg were also included. Each study utilized 6 to 8 mice per group.
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In Vitro Model | Breast adenocarcinoma | MDA-MB-231 cells | CVCL_0062 | ||
Breast adenocarcinoma | HCC1428 cells | CVCL_1252 |
References
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