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D&D Pharmatech CEO Lee Seul-ki added that the FDA's approval for the phase 2 trial of NLY01 in MS reflects the notable disease-modifying effects we observed in younger patients during our phase 2 Parkinson's trial, which was built on years of preclinical collaboration with Johns Hopkins University School of Medicine

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This is a meaningful mechanistic observation that contributes to the broader fat-loss narrative around the compound

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[40] report that oral ALA supplementation (1200 mg/12 weeks) resulted in a significant reduction in the serum leptin concentration and a noticeable elevation in the adiponectin-to-leptin ratio in patients with non-alcoholic fatty liver disease

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