Home › Mild Cognitive Impairment › NCT05606341
Innate Immunity Stimulation Via TLR9 in Early AD
Phase 1 Clinical Trial of Innate Immunity Stimulation Via TLR9 in Early Alzheimer's Disease (AD)
Who can join
Ages 60 to 85 · All sexes
Full eligibility criteria
Inclusion Criteria: 1. 65-85 years of age 2. MCI due to AD or mild AD dementia per NIA-AA specified criteria published in 2018 3. Montreal Cognitive Assessment (MoCA) score ≥17 AND; 4. Positive Florbetaben PET amyloid scan, or other positive PET amyloid scan performed within one year of study enrollment 5. Must be able to provide consent or assent (If applicable). 6. Must be willing and able to participate in all study related procedures. 7. Must have a reliable study partner to provide information on the subject's cognitive and functional status. Study partner must have sufficient contact with the subject, as determined by the PI, and be available to accompany the subject to clinic visits or by phone. Exclusion Criteria: 1. History of psychiatric illness (e.g. hallucinations, major depression, suicidal ideation or delusions) that could interfere with completion of study related procedures as determined by PI 2. History of autoimmune disorders or antibody-mediated disease, severe asthma, or other serious infection or systemic illness, as determined by PI 3. Use of corticosteroids or immunosuppressive drugs within 30 days of study entry 4. History of splenectomy 5. Renal impairment 6. Use of chloroquine within 8 weeks of study entry 7. Inability to undergo MRI imaging 8. History of TIA, stroke or seizures within 12 months of screening 9. Any neurological condition other than AD that could contribute to cognitive impairment (including related to possible "long COVID") as determined by PI 10. Participation in any other current AD investigational interventional trial 11. Current use of an anti-coagulant 12. Current use of drugs that are major substrates of cytochrome P450 (CYP) enzyme 1A2 13. Recent exposure to COVID-19 infection within 14 days or recent onset of symptoms within 14 days that may be related to COVID-19 infection
About the study
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.
What is being tested
- CpG1018 (drug)
- CpG1018 (drug)
- CpG1018 (drug)
- Placebo (drug)
Sponsor: NYU Langone Health · Participants: 18 · Started: Mar 13, 2023
Contact the study team
- Anaztasia Ulysse · Phone: 212-263-0771
- Dylan Nelson · Phone: 212-263-5845
Official record on ClinicalTrials.gov — NCT05606341
Locations in the U.S.
| New York | NYU Langone Health, New York |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.