4.0 Article

Zimberelimab

Journal

DRUGS OF THE FUTURE
Volume 47, Issue 2, Pages 115-121

Publisher

PROUS SCIENCE, SAU-THOMSON REUTERS
DOI: 10.1358/dof.2022.47.2.3400575

Keywords

Zimberelimab; AB-122; GLS-010; Monoclonal; antibody -; PD-1-; Solid tumors; Hodgkin lymphoma

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Immune checkpoint inhibitors, such as Zimberelimab, have shown potential in the treatment of solid tumors. Zimberelimab exhibits similar activity and selectivity to currently approved PD-1 inhibitors and shows particular benefit in tumors with PD-L1 and TMB positivity. Various early phase clinical trials are investigating its safety and efficacy in different treatment regimens.
Immune checkpoint inhibitors, including those targeting the programmed cell death protein 1 receptor (PD-1) and ligand (PD-L1), have shown promise in the treatment of advanced, relapsed and refractory solid tumors. Zimberelimab (also known as AB-122 or GLS-010) is a fully human immunoglobulin G4 monoclonal antibody against the PD-1 receptor being developed by Arcus Biosciences (AB-122) and Harbin Gloria Pharmaceuticals (GLS-010) for the treatment of advanced solid tumor cancers. Preclinical investigations show zimberelimab has a similar activity and selectivity profile to currently approved PD-1 inhibitors. Early data from phase I studies show similar rates of treatment-related adverse events and suggest particular benefit in tumors with PD-L1 and tumor mutation burden (TMB) biomarker positivity. Many early phase clinical trials are investigating its safety and efficacy in a variety of regimens, including as monotherapy, in combination with standard chemotherapies, and in combination with other immunotherapeutic agents targeting the tumor microenvironment.

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