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Clinical Trial Summary

This single-center, double-blind, placebo-controlled study will recruit in total 39 participants with either Mild Cognitive Impairment due to Alzheimer's disease (MCI) or Mild Alzheimer's disease dementia (mild AD). There will be 3 Dose levels. An initial cohort of 13 subjects will be randomized to a Dose level 1 (0.1 mg/kg vs. placebo) lasting 8 weeks. An additional 13 subjects will be recruited and randomized into Dose level 2 (0.25 mg/kg vs. placebo) for 8 weeks and 13 subjects for the last Dose level 3 (0.5 mg/kg vs. placebo) for 8 weeks. The primary objective will be to assess safety and tolerability of CpG 1018.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05606341
Study type Interventional
Source NYU Langone Health
Contact Alok Vedvyas
Phone 212-263-2048
Email Alok.Vedvyas@nyulangone.org
Status Recruiting
Phase Phase 1
Start date March 13, 2023
Completion date November 2025

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