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Positive efficacy signals in a challenging 3L NSCLC setting, coupled with completed Part C enrollment, can reduce clinical risk and attract attention from investors. However, the small sample size and reliance on DCR in a single arm warrant caution; upside depends on confirmatory data and durability of response.
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MAIA announced positive Phase 2 THIO-101 Part C data in third-line NSCLC, showing a 90.5% disease control rate (19/21) with ateganosine followed by cemiplimab. The results, consistent with Parts A/B and in a more heavily pre-treated population, may support a faster path to broader evaluation and potential near-term upside in MAIA shares.
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