Drug intelligence / Profile preview

osimertinib + sintilimab

Development stage
Preclinical
Lead developer
AstraZeneca
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules, Vaccines & Immunotherapeutics
Administration
Oral, Intravenous
01

Overview

Osimertinib + sintilimab is an investigational combination therapy for cancer treatment. Osimertinib is a third-generation small molecule epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) that selectively targets both EGFR-sensitizing mutations and the T790M resistance mutation in non-small cell lung cancer (NSCLC). Sintilimab is a monoclonal antibody that acts as an immune checkpoint inhibitor by targeting programmed cell death protein 1 (PD-1), thereby enhancing anti-tumor immune responses. This combination aims to address acquired resistance to EGFR-TKIs in patients with EGFR-mutant NSCLC by combining targeted inhibition of tumor growth signaling with immunotherapy-mediated enhancement of anti-tumor immunity. The combination has been explored primarily in clinical trials for patients who have progressed after prior EGFR-TKI therapy[3][6].

Other names
osimertinib + sintilimab
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)EGFR T790M (Epidermal growth factor receptor T790M mutant)

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