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Far from being a single procedural step, a FIH trial is built on a broad body of scientific, regulatory and operational work designed to ensure that the transition from preclinical research to human investigation takes place within a rigorous framework focused on safety, quality and evidence generation
Human clinical data remains limited for both forms
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[DOI] [PMC free article] [PubMed] [Google Scholar] 272.Lykkesfeldt J., Tveden-Nyborg P
The individual components of KLOW have been studied extensively in research settings with favorable safety profiles
Many users report that the benefits become more noticeable over time
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