Therapeutic | Lirilumab |
Target | KIRD2 |
Heavy Chain | QVQLVQSGAEVKKPGSSVKVSCKASGGTFSFYAISWVRQAPGQGLEWMGGFIPIFGAANYAQKFQGRVTITADESTSTAYMELSSLRSDDTAVYYCARIPSGSYYYDYDMDVWGQGTTVTVSS |
Light Chain | EIVLTQSPVTLSLSPGERATLSCRASQSVSSYLAWYQQKPGQAPRLLIYDASNRATGIPARFSGSGSGTDFTLTISSLEPEDFAVYYCQQRSNWMYTFGQGTKLEIK |
100% seqID Fv Structure | None |
99% seqID Fv Structure | None |
95-98% seqID Fv Structure | None |
Follow these links to our prediction tools:
Format | Whole mAb |
Isotype | G4 |
Highest Clinical Trial (January '23) | Phase-II |
Estimated Status (January '23) | Active |
Recorded Developmental Technology | Medarex UltiMAb Mouse |
INN Year Proposed | 2012 |
INN Year Recommended | 2013 |
Companies Involved | Novo Nordisk, Bristol-Myers Squibb, Dana-Farber Cancer Institute, Innate Pharma, National Cancer Institute (USA), Ono Pharmaceutical, PrECOG, University of Texas M. D. Anderson Cancer Center |
Conditions Approved | na |
Conditions Active | Chronic lymphocytic leukaemia, Head and neck cancer, Myelodysplastic syndromes, Solid tumours, Bladder cancer |
Conditions Discontinued | Acute myeloid leukaemia, Hepatitis C, Haematological malignancies, Multiple myeloma, Lymphoma |
Notes |
SAbDab papers
Schneider, C., Raybould, M.I.J., Deane, C.M. (2022) SAbDab in the Age of Biotherapeutics: Updates including SAbDab-Nano, the Nanobody Structure Tracker. Nucleic Acids Res. 50(D1):D1368-D1372 [link]
Dunbar, J., Krawczyk, K. et al. (2014) SAbDab: the Structural Antibody Database. Nucleic Acids Res. 42(D1):D1140-D1146 [link]
Thera-SAbDab paper
Raybould, M.I.J., Marks, C. et al (2020) Thera-SAbDab: the Therapeutic Structural Antibody Database. Nucleic Acids Res. 48(D1):D383-D388. [link]