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clinical-trial

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The method presented is used by pharmaceutical regulatory authorities to detect data manipulation in clinical trials (bioequivalence). The code shown makes it possible to use the PK data of a clinical study to determine which blood samples may have been illegally reanalysed in order to positively influence the result of the study.

  • Updated Dec 2, 2024
  • R

Research project investigating lithium deficiency as a contributor to Alzheimer's disease and low-dose lithium orotate supplementation for cognitive protection. Includes Phase 1 clinical trial documentation, IRB protocols, evidence synthesis, and literature review based on 2025 Nature findings.

  • Updated Mar 13, 2026

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