Drug intelligence / Profile preview

aur106

Development stage
Phase 1
Lead developer
Aurigene Oncology
Modality
Small Molecules
Administration
Oral
01

Overview

AUR106 is an orally bioavailable small molecule inhibitor that targets both TIGIT (T-cell immunoreceptor with immunoglobulin and ITIM domains) and PD-L1 (programmed death-ligand 1), two key immune checkpoint proteins involved in tumor immune evasion. By simultaneously inhibiting TIGIT and PD-L1, AUR106 aims to enhance anti-tumor immune responses by blocking inhibitory signals that suppress T-cell activity. Developed from Aurigene's small molecule immuno-oncology platform, AUR106 offers potential advantages over antibody-based therapies, such as oral administration, ease of combination dosing, improved management of immune-related adverse events, and lower cost of goods. The drug is currently in Phase 1 clinical trials for various advanced solid tumors including non-small cell lung cancer, gastric cancer, urothelial cancer (including advanced urothelial carcinoma), kidney cancer, colon cancer, esophageal cancer, gastrointestinal cancers, colorectal cancer and transitional cell carcinoma.

02

Targets

TIGIT (T cell immunoreceptor with Ig and ITIM domains)CD274 (Programmed cell death protein 1 ligand 1)

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