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FDA granted Fast Track designation for NSCLC treatment, while MAIA entered a master clinical supply agreement with Roche, leading to international trial expansion.

1 report, 1 independent Updated Aug 18
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What happened

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FDA granted Fast Track designation for NSCLC treatment, while MAIA entered a master clinical supply agreement with Roche, leading to international trial expansion.

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How it developed

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  1. MAIA Biotechnology began clinical trials, dosing the first patient in Taiwan and screening in Europe and Asia, with Regeneron providing Libtayo.Sub-event
  2. MAIA received Fast Track designation from the FDA for NSCLC treatment and expanded trials into Europe.1 source

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  • GlobeNewswireDiamond Equity Research Releases Update Note on MAIA Biotechnology, Inc. (NYSE: MAIA) New York, Aug. 18, 2025 (GLOBE NEWSWIRE) -- Diamond Equity Research, a leading equity research firm with a focus