Drug intelligence / Profile preview

ATG-107

Development stage
Preclinical
Lead developer
Antengene
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, T-cell Engagers → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics
Administration
Intravenous, Subcutaneous
01

Overview

ATG-107 is a bispecific T-cell engager (TCE) developed by Antengene. It utilizes a novel "2+1" format to simultaneously target FLT3 (Fms-like tyrosine kinase 3), which is overexpressed in the majority of acute myeloid leukemia (AML) cases, and CD3 on T cells. The molecule binds bivalently to FLT3, concealing the CD3 binding site until FLT3 engagement occurs, thereby redirecting T cells to attack AML cells with high specificity and minimizing off-target activation. Preclinical studies have demonstrated potent FLT3-dependent T-cell activation and cytotoxicity against AML cells regardless of their FLT3 mutation status, as well as strong anti-leukemic efficacy in humanized mouse models. The AnTenGager™ platform underlying ATG-107 aims to reduce systemic CD3 activation and cytokine release syndrome risk compared to conventional approaches[1][4][5][6].

02

Targets

CD3 (T-cell surface glycoprotein CD3)FLT3 (Fms related receptor tyrosine kinase 3)

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