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  "documentTitle": "argenx SE | Results Presentation Deck | 16 slides",
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      "text": "Safety and Tolerability: Well-tolerated with safety profile consistent with prior clinical trials and confirmed profile of VYVGART",
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      "text": "Primary Endpoint: Study met primary endpoint (p=0.000039); VYVGART Hytrulo demonstrated a 61% reduction (HR: 0.39 95% CI: 0.25; 0.61) in the risk of relapse compared to placebo based on time to first adjusted INCAT deterioration",
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