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In two studies, Withaar et al

Eli Lilly has not announced a specific regulatory submission timeline, but Phase 3 completion and FDA filing would logically follow several years behind CagriSemas timeline

To integrate evidence across datasets, we performed a meta-analysis combining MR estimates from all cohorts, which allowed us to strengthen statistical power, assess effect consistency, and ensure the robustness of the observed associations across diverse populations

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This hypothesis is supported by early trial data but requires confirmation in larger Phase 3 studies