Drug intelligence / Profile preview

ZL-1310 + atezolizumab

Development stage
Unknown
Lead developer
Zai Lab
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

ZL-1310 + atezolizumab is an investigational combination therapy under study for the treatment of extensive-stage small cell lung cancer (ES-SCLC) and potentially other neuroendocrine tumors that express delta-like ligand 3 (DLL3)[3][7]. ZL-1310 is a first-in-class antibody-drug conjugate (ADC) composed of a humanized anti-DLL3 monoclonal antibody linked to a novel camptothecin derivative, engineered to selectively target DLL3, an antigen overexpressed in SCLC and other neuroendocrine cancers[7]. Atezolizumab (Tecentriq) is a fully humanized IgG1 monoclonal antibody immune checkpoint inhibitor that binds to programmed death-ligand 1 (PD-L1), blocking its interaction with PD-1 and B7.1 receptors, resulting in reactivation of T-cells and restoration of anti-tumor immune responses[2][7][6]. The combination aims to couple the direct cytotoxicity of the DLL3-targeted ADC with immune activation and reversal of tumor immunosuppression via PD-L1 blockade.

Brand names
Tecentriq
Other names
ZL-1310 + Tecentriq
02

Targets

TOP1 (DNA Topoisomerase I)CD274 (Programmed cell death protein 1 ligand 1)DLL3 (Delta-like ligand 3)

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