Antibody Information
General Information of This Antibody
Antibody ID | ANI0VVOSK |
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Antibody Name | Samrotamab |
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Organization | AbbVie, Inc. |
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Indication | Solid tumors |
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Synonyms |
PR-1498487
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Antibody Type | Monoclonal antibody (mAb) |
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Antibody Subtype | Chimeric IgG1-kappa |
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Antigen Name | Leucine-rich repeat-containing protein 15 (LRRC15) |
Antigen Info | ||||
Click to Show/Hide the Sequence Information of This Antibody | ||||||
Heavy Chain Sequence |
EVQLVQSGAEVKKPGASVKVSCKASGYKFSSYWIEWVKQAPGQGLEWIGEILPGSDTTNY
NEKFKDRATFTSDTSINTAYMELSRLRSDDTAVYYCARDRGNYRAWFGYWGQGTLVTVSS ASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSS GLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGG PSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYN STYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREE MTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRW QQGNVFSCSVMHEALHNHYTQKSLSLSPGK Click to Show/Hide
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Heavy Chain Varible Domain |
EVQLVQSGAEVKKPGASVKVSCKASGYKFSSYWIEWVKQAPGQGLEWIGEILPGSDTTNY
NEKFKDRATFTSDTSINTAYMELSRLRSDDTAVYYCARDRGNYRAWFGYWGQGTLVTVSS Click to Show/Hide
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Heavy Chain Constant Domain 1 |
ASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSS
GLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKV Click to Show/Hide
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Heavy Chain Constant Domain 2 |
APELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTK
PREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAK Click to Show/Hide
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Heavy Chain Constant Domain 3 |
GQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDS
DGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK Click to Show/Hide
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Heavy Chain Hinge Region |
EPKSCDKTHTCPPCP
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Heavy Chain CDR 1 |
GYKFSSYW
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Heavy Chain CDR 2 |
ILPGSDTT
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Heavy Chain CDR 3 |
ARDRGNYRAWFGY
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Light Chain Sequence |
DIQMTQSPSSLSASVGDRVTITCRASQDISNYLNWYQQKPGGAVKFLIYYTSRLHSGVPS
RFSGSGSGTDYTLTISSLQPEDFATYFCQQGEALPWTFGGGTKVEIKRTVAAPSVFIFPP SDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLT LSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC Click to Show/Hide
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Light Chain Varible Domain |
DIQMTQSPSSLSASVGDRVTITCRASQDISNYLNWYQQKPGGAVKFLIYYTSRLHSGVPS
RFSGSGSGTDYTLTISSLQPEDFATYFCQQGEALPWTFGGGTKVEIK Click to Show/Hide
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Light Chain Constant Domain |
RTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQD
SKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC Click to Show/Hide
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Light Chain CDR 1 |
QDISNY
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Light Chain CDR 2 |
YTS
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Light Chain CDR 3 |
QQGEALPWT
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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
Samrotamab vedotin [Phase 1]
Identified from the Human Clinical Data
Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
Efficacy Data | Objective Response Rate (ORR) |
2.10% (non-sarcomas all doses)
10.80% (sarcomas all dose) 20.00% (osteosarcoma+UPS 3.6 mg/kg) 20.00% (osteosarcoma 3.6 mg/kg) 20.00% (UPS 3.6 mg/kg) |
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Patients Enrolled |
Patients with LRRC15 positive squamous cell carcinoma of the head and neck, NSCKC, breast cancer, undifferentiated pleomorphic sarcoma or osteosarcoma.
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Administration Dosage |
0.30 up to 6.00 mg/kg on day 1, once every 2 weeks.
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Related Clinical Trial | |||||
NCT Number | NCT02565758 | Clinical Status | Phase 1 | ||
Clinical Description |
A multicenter, phase 1, open-label, dose-escalation study of ABBV-085, an antibody drug conjugate, in subjects with advanced solid tumors.
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Experiment 2 Reporting the Activity Date of This ADC | [2] | ||||
Related Clinical Trial | |||||
NCT Number | NCT02565758 | Clinical Status | Phase 1 | ||
Clinical Description |
A multicenter, phase 1, open-label, dose-escalation study of ABBV-085, an antibody drug conjugate, in subjects with advanced solid tumors.
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Discovered Using Patient-derived Xenograft Model
Experiment 1 Reporting the Activity Date of This ADC | [3] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 27.90% (Day 20) | Negative LRRC15 (LRRC15-) | ||
Method Description |
The efficacy of ABBV-085 directed against LRRC15 was assessed in several patient-derived xenograft models of UPS,LMS,and DDLPS. For efficacy study,tumors were allowed to establish to 200±50 mm3 in size before randomization into various treatment groups with 7-9 mice per group. Isotype-control,isotype-MMAE,and ABBV-085,diluted in PBS were administered at 6 mg/kg once every 4 days intraperitoneally for a total of six injections.
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In Vivo Model | Liposarcoma PDX model (PDX: LPS28) | ||||
Experiment 2 Reporting the Activity Date of This ADC | [3] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 34.50% (Day 22) | Negative LRRC15 (LRRC15-) | ||
Method Description |
The efficacy of ABBV-085 directed against LRRC15 was assessed in several patient-derived xenograft models of UPS,LMS,and DDLPS. For efficacy study,tumors were allowed to establish to 200±50 mm3 in size before randomization into various treatment groups with 7-9 mice per group. Isotype-control,isotype-MMAE,and ABBV-085,diluted in PBS were administered at 6 mg/kg once every 4 days intraperitoneally for a total of six injections.
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In Vivo Model | Leiomyosarcoma PDX model (PDX: LMS33) | ||||
Experiment 3 Reporting the Activity Date of This ADC | [3] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 38.10% (Day 43) | Negative LRRC15 (LRRC15-) | ||
Method Description |
The efficacy of ABBV-085 directed against LRRC15 was assessed in several patient-derived xenograft models of UPS,LMS,and DDLPS. For efficacy study,tumors were allowed to establish to 200±50 mm3 in size before randomization into various treatment groups with 7-9 mice per group. Isotype-control,isotype-MMAE,and ABBV-085,diluted in PBS were administered at 6 mg/kg once every 4 days intraperitoneally for a total of six injections.
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In Vivo Model | Liposarcoma PDX model (PDX: LPS28) | ||||
Experiment 4 Reporting the Activity Date of This ADC | [3] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 87.20% (Day 20) | High LRRC15 expression (LRRC15+++) | ||
Method Description |
The efficacy of ABBV-085 directed against LRRC15 was assessed in several patient-derived xenograft models of UPS,LMS,and DDLPS. For efficacy study,tumors were allowed to establish to 200±50 mm3 in size before randomization into various treatment groups with 7-9 mice per group. Isotype-control,isotype-MMAE,and ABBV-085,diluted in PBS were administered at 6 mg/kg once every 4 days intraperitoneally for a total of six injections.
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In Vivo Model | Liposarcoma PDX model (PDX: LPS28) | ||||
Experiment 5 Reporting the Activity Date of This ADC | [3] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 88.70% (Day 25) | High LRRC15 expression (LRRC15+++) | ||
Method Description |
The efficacy of ABBV-085 directed against LRRC15 was assessed in several patient-derived xenograft models of UPS,LMS,and DDLPS. For efficacy study,tumors were allowed to establish to 200±50 mm3 in size before randomization into various treatment groups with 7-9 mice per group. Isotype-control,isotype-MMAE,and ABBV-085,diluted in PBS were administered at 6 mg/kg once every 4 days intraperitoneally for a total of six injections.
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In Vivo Model | Leiomyosarcoma PDX model (PDX: LMS33) | ||||
Experiment 6 Reporting the Activity Date of This ADC | [3] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 95.20% (Day 21) | High LRRC15 expression (LRRC15+++) | ||
Method Description |
The efficacy of ABBV-085 directed against LRRC15 was assessed in several patient-derived xenograft models of UPS,LMS,and DDLPS. For efficacy study,tumors were allowed to establish to 200±50 mm3 in size before randomization into various treatment groups with 7-9 mice per group. Isotype-control,isotype-MMAE,and ABBV-085,diluted in PBS were administered at 6 mg/kg once every 4 days intraperitoneally for a total of six injections.
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In Vivo Model | Leiomyosarcoma and undifferentiated sarcomas PDX model, (PDX: UPS7) | ||||
Experiment 7 Reporting the Activity Date of This ADC | [3] | ||||
Efficacy Data | Tumor Growth Inhibition value (TGI) | ≈ 100.00% (Day 22) | High LRRC15 expression (LRRC15+++) | ||
Method Description |
The efficacy of ABBV-085 directed against LRRC15 was assessed in several patient-derived xenograft models of UPS,LMS,and DDLPS. For efficacy study,tumors were allowed to establish to 200±50 mm3 in size before randomization into various treatment groups with 7-9 mice per group. Isotype-control,isotype-MMAE,and ABBV-085,diluted in PBS were administered at 6 mg/kg once every 4 days intraperitoneally for a total of six injections.
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In Vivo Model | Leiomyosarcoma and undifferentiated sarcomas PDX model, (PDX: UPS7) |
References
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