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  "documentTitle": "MAIA Biotechnology | Investor Presentation Deck | 39 slides",
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  "authorName": "MAIA Biotechnology",
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  "sourceTypeLabel": "Investor relations",
  "presentationDate": "2023-10-01 00:00:00",
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  "notes": "Data presented in a table format with specific clinical definitions for DCR and treatment lines.",
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      "text": "*At study entry **CR/PR/SD at 1st Post Baseline Scan ***Includes all subjects with at least 1 post baseline assessment at the time of the cut-off. No subjects discontinued due to disease progression prior to first scan",
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      "text": "Disease control was reported in 34 of 37 subjects (92%) with at least one post baseline assessment, including 19 of 19 subjects (100%) in 2nd line and 14 of 16 subjects (88%) in 3rd line",
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      "text": "By dose level, Disease control was reported in 11 of 13 subjects (85%) assigned THIO 360 mg/cycle, 11 of 11 subjects (100%) assigned THIO 180 mg/cycle, and 12 of 13 subjects (92%) assigned THIO 60 mg/cycle",
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      "text": "All dose levels being tested already met DCR required in Stage 1 to warrant further investigation (DCR ≥8 of 19 subjects)",
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      "text": "DCR, [defined as CR, PR, or SD per RECIST 1.1 at Cycle 3 Day 1 (6 weeks)] met the pre-determined statistical requirements per protocol to proceed to Stage 2. However, the data is not mature yet to assess the ORR",
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      "text": "DISEASE CONTROL",
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