Drug intelligence / Profile preview

ateganosine

Development stage
Phase 3
Lead developer
Maia Biotechnology
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Metabolically Activated Prodrugs → Prodrugs/Conditional Activator Small Molecules → Small Molecules, DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

Ateganosine is a first-in-class telomere-targeting small molecule anticancer agent developed by MAIA Biotechnology. Its mechanism involves inducing telomerase-dependent modification of telomeric DNA in cancer cells, leading to their death. Ateganosine also activates immune responses through both the innate cGAS/STING pathway and adaptive T-cell immunity. In preclinical studies and ongoing clinical trials, ateganosine has demonstrated potential for significant tumor regression and induction of cancer-specific immune memory when combined with PD-(L)1 inhibitors such as cemiplimab (Libtayo). It is being developed primarily for advanced non-small cell lung cancer (NSCLC) patients with telomerase-positive tumors who are resistant to standard checkpoint inhibitor therapies[8][10][6].

Other names
THIO6-thio-2'-deoxyguanosine
02

Targets

Neuraminidase

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