Drug intelligence / Profile preview

surovatamig

Development stage
Phase 3
Lead developer
AstraZeneca
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Subcutaneous
01

Overview

Surovatamig is a fully human IgG4 bispecific monoclonal antibody that acts as a T-cell engager, targeting both **CD19** on malignant B cells and **CD3** on cytotoxic T lymphocytes. By binding simultaneously to CD19 and CD3, it redirects and activates cytotoxic T cells to kill malignant B cells. Surovatamig is engineered to bind CD3 with lower affinity than some previous T-cell engagers, which is intended to reduce risks such as excessive cytokine release and neurotoxicity. It is being developed primarily for the treatment of **relapsed or refractory B-cell acute lymphoblastic leukaemia (r/r B-ALL)** after two or more prior therapies in both adolescents and adults, but is also in clinical trials for other B-cell malignancies including follicular lymphoma and non-Hodgkin lymphoma. It is administered intravenously or subcutaneously. The drug was originally developed by TeneoTwo and TeneoBio and is currently being developed by AstraZeneca[1][2][3][4][5][7].

Brand names
surovatamig
Other names
AZD0486AZD-0486AZD 0486TNB-486TNB486TNB 486
02

Targets

CD19 (B lymphocyte antigen CD19)CD3 (T-cell surface glycoprotein CD3)

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