NCT05225415CompletedPhase 2
Study to Evaluate the Safety, Tolerability and Efficacy of CT1812 in Subjects With Mild to Moderate Dementia With Lewy Bodies
A Randomized, Double-blind, Placebo-controlled, Phase 2, 6-month Study to Evaluate the Safety, Tolerability and Exploratory Efficacy of CT1812 in Subjects With Mild to Moderate Dementia With Lewy Bodies
Source: ClinicalTrials.gov · Last updated 12 Mar 2026
Brief summary (registry, in English)
Multi-center, randomized, double-blind, placebo-controlled, 6- month study in subjects with mild to moderate Dementia with Lewy Bodies.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 130 (actual)
- First submitted
- 11 Jan 2022
- Start date
- 19 May 2022
- Primary completion date
- 25 Nov 2024
- Lead sponsor
- Cognition Therapeutics
- Diseases
- Lewy body dementia
- NCT number
- NCT05225415
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 130
- From 19 May 2022 to the primary completion date, 25 Nov 2024
- 34 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Screening MRI (or historical MRI or CT scan due to contraindication of MRI if approved by medical monitor) or historical MRI/CT scan, if applicable. of the brain indicative of significant abnormality, including, but not limited to, prior hemorrhage or infarct \> 1 cm3, \>3 lacunar infarcts, cerebral contusion, encephalomalacia, aneurysm, vascular malformation, subdural hematoma, hydrocephalus, space-occupying lesion (e.g. abscess or brain tumor such as meningioma). If a small incidental meningioma is observed, the medical monitor may be contacted to discuss eligibility.
Other illness
- Any neurological condition that may be contributing to cognitive impairment above and beyond those caused by the subject's DLB, including any co-morbidities detected by clinical assessment or MRI (or CT scan due to contraindication of MRI, if approved by medical monitor)
- Any major psychiatric diagnosis, including schizophrenia, bipolar disorder, and current major depressive disorder as per Diagnostic and Statistical Manual of Mental Disorders Fifth Edition
- Clinically significant, advanced or unstable disease that may interfere with outcome evaluations.
Lab values
- Clinical, laboratory findings or medical history consistent with:
- Other primary degenerative dementia (fronto-temporal dementia, Huntington's disease, Creutzfeldt-Jakob Disease, Down syndrome, etc.).
- Other neurodegenerative condition (amyotrophic lateral sclerosis, etc.).
- Seizure disorder.
- Other infectious, metabolic or systemic diseases affecting the central nervous system (syphilis, present hypothyroidism, present vitamin B12 or folate deficiency, other laboratory values etc.).
Who the study is looking for
- Men or women 50-85 years of age (inclusive), meeting criteria for probable Dementia with Lewy Bodies (DLB).
- MRI, or CT scan due to contraindication of MRI if approved by medical monitor) obtained during screening consistent with the clinical diagnosis of DLB and without findings of significant exclusionary abnormalities. An historical MRI (or CT scan), up to 1 year prior to screening, may be used if there is no history of intervening neurologic disease or clinical events (such as a stroke, head trauma etc.) and the subject is without clinical symptoms or signs suggestive of such intervening events.
- MMSE 18-27 inclusive
Age in the registry: 50 years to 85 years · Sex: All · Does not accept healthy volunteers
Sites (34)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| JEM Research Institute Coordinator of this site? Confirm its status | Atlantis | United States | Unknown status |
| University of Colorado Coordinator of this site? Confirm its status | Aurora | United States | Unknown status |
| Parkinson's Disease and Movement Disorders Center of Boca Raton Coordinator of this site? Confirm its status | Boca Raton | United States | Unknown status |
| University of Miami Miller School of Medicine Comprehensive Center for Brain Health Coordinator of this site? Confirm its status | Boca Raton | United States | Unknown status |
| UNC Department of Neurology Coordinator of this site? Confirm its status | Chapel Hill | United States | Unknown status |
| University of Virginia Adult Neurology Coordinator of this site? Confirm its status | Charlottesville | United States | Unknown status |
| Rush University Medical Center Section of Parkinson Disease and Movement Disorder Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
| Cleveland Clinic - Main Campus Coordinator of this site? Confirm its status | Cleveland | United States | Unknown status |
| Ohio State University Coordinator of this site? Confirm its status | Columbus | United States | Unknown status |
| University of Texas, Southwestern Coordinator of this site? Confirm its status | Dallas | United States | Unknown status |
| CenExel Rocky Mountain Clinical Research, LLC Coordinator of this site? Confirm its status | Englewood | United States | Unknown status |
| The University of Kansas Alzheimer's Disease Research Center Coordinator of this site? Confirm its status | Fairway | United States | Unknown status |
| Clinical Trial Network Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
| Josephson Wallack Munshower Neurology P.C. Coordinator of this site? Confirm its status | Indianapolis | United States | Unknown status |
| IU Health Neuroscience Center, Goodman Hall Coordinator of this site? Confirm its status | Indianapolis | United States | Unknown status |
| Evergreen Health Research Coordinator of this site? Confirm its status | Kirkland | United States | Unknown status |
| Charter Research Coordinator of this site? Confirm its status | Lady Lake | United States | Unknown status |
| University of Kentucky Coordinator of this site? Confirm its status | Lexington | United States | Unknown status |
| Columbia University Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Renstar Medical Research Coordinator of this site? Confirm its status | Ocala | United States | Unknown status |
| Stanford University Coordinator of this site? Confirm its status | Palo Alto | United States | Unknown status |
| University of Pennsylvania Coordinator of this site? Confirm its status | Philadelphia | United States | Unknown status |
| Barrow Neurological Institute Coordinator of this site? Confirm its status | Phoenix | United States | Unknown status |
| Headlands Research Eastern Massachusetts, LLC Coordinator of this site? Confirm its status | Plymouth | United States | Unknown status |
| Oregon Health and Science University Coordinator of this site? Confirm its status | Portland | United States | Unknown status |
| Summit Headlands LLC Coordinator of this site? Confirm its status | Portland | United States | Unknown status |
| Virginia Commonwealth University Coordinator of this site? Confirm its status | Richmond | United States | Unknown status |
| Mayo Clinic Coordinator of this site? Confirm its status | Rochester | United States | Unknown status |
| Pacific Neuroscience Institute Coordinator of this site? Confirm its status | Santa Monica | United States | Unknown status |
| Universtiy of Washington Department of Neurology Coordinator of this site? Confirm its status | Seattle | United States | Unknown status |
| New England Institute for Neurology and Headache (NEINH) Coordinator of this site? Confirm its status | Stamford | United States | Unknown status |
| Banner Sun Health Research Institute Coordinator of this site? Confirm its status | Sun City | United States | Unknown status |
| University of Arizona Health Sciences Center Coordinator of this site? Confirm its status | Tucson | United States | Unknown status |
| Charter Research Coordinator of this site? Confirm its status | Winter Park | United States | Unknown status |
Related publications
- Phase 2 study of zervimesine (CT1812) in participants with mild-to-moderate dementia with Lewy bodies (DLB).Alzheimers Dement · 2025 · PMID 41416579
This page is information, not medical advice. Discuss any trial with your doctor.