MAIA Biotechnology Initiates Phase 3 Trial for ATEG in NSCLC
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Dec 11 2025
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Source: Newsfilter
- Clinical Advancement: MAIA Biotechnology's ATEG (6-thio-2'-deoxyguanosine) shows promising results in advanced non-small cell lung cancer (NSCLC) during Phase 2 trials, with the initiation of Phase 3 trials this week indicating substantial market potential.
- FDA Fast Track: The therapy has received Fast Track designation from the FDA, highlighting its uniqueness in NSCLC treatment and suggesting a very high probability of regulatory success, which could expedite its market entry.
- Dual Mechanism: ATEG operates through a dual mechanism by selectively integrating into cancer cell telomeres and activating immune responses, offering a distinct treatment approach compared to existing therapies and potentially paving the way for broader solid tumor indications.
- Market Opportunity: Given the significant demand in the NSCLC market, ATEG, as the first telomere-targeting agent, could emerge as a major player in next-generation cancer treatment if clinical results are confirmed, significantly enhancing MAIA's market position.
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Analyst Views on MAIA
Wall Street analysts forecast MAIA stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for MAIA is 14.00 USD with a low forecast of 14.00 USD and a high forecast of 14.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.
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Current: 2.390
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About MAIA
MAIA Biotechnology, Inc. is a clinical-stage biopharmaceutical company developing targeted immunotherapies for cancer. The Company's THIO (6-thio-dG, 6-thio-2'-deoxyguanosine), is a lead asset, is an investigational dual mechanism of action drug candidate incorporating telomere targeting and immunogenicity. The modified nucleotide 6-thio-2-deoxyguanosine (THIO) induces telomerase-dependent telomeric DNA modification, DNA damage responses, and selective cancer cell death. THIO-damaged telomeric fragments accumulate in cytosolic micronuclei and activates both innate (cGAS/STING) and adaptive (T-cell) immune responses. The sequential treatment with THIO followed by PD-(L)1 inhibitors resulted in tumor regression in advanced, in vivo cancer models by induction of cancer type-specific immune memory. THIO is being developed as a second or later line of treatment for NSCLC for patients that have progressed beyond the standard-of-care regimen of existing checkpoint inhibitors.
About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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