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References 1-Smith, R

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In contrast, several studies included in this review that enrolled younger individuals or participants with milder symptom profile have documented improvements following EPA/DHA supplementation, suggesting that age, developmental stage, and baseline severity may critically modulate treatment responsiveness

The doses used in neurological models in animals fall within the same general range as musculoskeletal studies, suggesting that a standard subcutaneous protocol at 250 to 500 micrograms per day would be the appropriate starting framework

1 Lilly expects to submit its FDA application of the new drug by the end of 2025

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