Vudalimab Biosimilar Bispecific Antibody (CTLA-4 × PD-1) for Research

Cat No.: GMP-Bios-ab-631

Pre-Made Vudalimab biosimilar, Bispecific Mixed mAb and scFv, Anti-CTLA4/CTLA-4;PDCD1/PD-1 Antibody: Anti-CD/GSE/GRD4/ALPS5/CD152/IDDM12/CELIAC3;CD279/SLEB2/hPD-1/hPD-l/hSLE1 therapeutic antibody is a biosimilar expressed by mammalian cell line as a benchmark reference therapeutic antibody for biological drug disovery items including cell culture, assay development, animal model development, PK/PD model development (Pharmacokinetics & Pharmacodynamic) and mechanism of action (MOA) research.

Vudalimab (formerly XmAb 20717 or XmAb 717) is a bispecific antibody being developed by Xencor, for the treatment of solid tumours. Xencor is using its Xtend Fc domain technology (a part of Xencor's proprietary XmAb® technology) that increases binding affinity to the receptor FcRn.

Order Information

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Catalog No. Package Price(In USD)
GMP-Bios-ab-631-1mg 1mg
GMP-Bios-ab-631-10mg 10mg
GMP-Bios-ab-631-100mg 100mg
GMP-Bios-ab-631-xmg >100mg



Product Details

Products Name (INN Index) Pre-Made Vudalimab biosimilar, Bispecific Mixed mAb and scFv, Anti-CTLA4/CTLA-4;PDCD1/PD-1 Antibody: Anti-CD/GSE/GRD4/ALPS5/CD152/IDDM12/CELIAC3;CD279/SLEB2/hPD-1/hPD-l/hSLE1 therapeutic antibody
INN Name Vudalimab
TargetCTLA-4;PD-1
FormatBispecific Mixed mAb and scFv
DerivationBispecific antibody
Species ReactivityHuman
CH1 IsotypeIgG1
VD LCKappa;Kappa
Highest_Clin_Trial (Jan '20)Phase-II
Est. StatusActive
100% SI StructureNone;None
99% SI StructureNone;None
95-98% SI Structure5tru:HL/5xj3:DE/6jc2:HL/6rp8:hl;None
Year Proposed2020
Year Recommended2021
CompaniesXencor
Conditions Approvedna
Conditions ActiveSolid tumours
Conditions Discontinuedna
Development Techna



About target - CTLA4

1. Protein Cytotoxic T-lymphocyte protein 4

2. Gene CTLA4

3. Organism Homo sapiens (Human)

Function
Inhibitory receptor acting as a major negative regulator of T-cell responses. The affinity of CTLA4 for its natural B7 family ligands, CD80 and CD86, is considerably stronger than the affinity of their cognate stimulatory coreceptor CD28.

Miscellaneous
The therapeutic antibody Ipilimumab competes for the binding site of the endogenous ligands CD80/B7-1, CD86/B7-2 and ICOSLG.