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  "notes": "The slide uses a structured layout with three distinct categories of safety findings (tolerability, SAEs, suicidality).",
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      "text": "Only SAE was in 50 µg dose group and deemed unrelated; AE profile consistent with historical studies and drug class",
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      "text": "No suicidal or self-injurious behavior; No indication of increased suicidality or suicide-related risk; ≤ 2 participants per arm reported suicidal ideation during the study",
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      "text": "Virtually all (99%) adverse events (AEs) were mild-to-moderate in severity; Minimal (2.5%) treatment emergent AEs (TEAEs) led to study withdrawal; No drug-related serious AEs (SAEs)",
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      "text": "1. Source: Study MMED008 internal study documents and calculations. Safety population. 2. One serious adverse event (SAE) was observed in the 50 µg dose group: panic attack on study day 98 that was deemed not related to treatment. 3. Suicidality assessment based on reported adverse events.",
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      "text": "MM120 Phase 2b was Well-tolerated with Mostly Expected Transient, Mild-to-Moderate Adverse Events on Dosing Day",
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