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Phase 2 N=130 Randomized Quadruple-blind Treatment

Study to Evaluate the Safety, Tolerability and Efficacy of CT1812 in Subjects With Mild to Moderate Dementia With Lewy Bodies

Dementia With Lewy Bodies

Enrolled (actual)
130
Serious AEs
13.2%
Results posted
Mar 2026
Primary outcome: Primary: Number of Study Participants With at Least One Mild, Moderate, or Severe Treatment Emergent Adverse Events (TEAEs) — 42; 40; 37; 14 participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
CT1812 (Drug)
Age
Adult, Older Adult · 50+ yrs
Sex
All
Sponsor
Cognition Therapeutics
Primary completion
Nov 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Study Participants With at Least One Mild, Moderate, or Severe Treatment Emergent Adverse Events (TEAEs)
42; 40; 37; 14; 21; 16
SECONDARY
Montreal Cognitive Assessment Scale (MoCA)
19.5; 17.8; 17.9; 19.4; 18.0; 18.2
SECONDARY
Epworth Sleepiness Scale (ESS)
7.9; 9.2; 8.2; 7.3; 9.6; 8.8
SECONDARY
Clinician Assessment of Fluctuation (CAF)
4.8; 5.9; 4.2; 4.3; 4.1; 4.9
SECONDARY
Alzheimer's Disease Cooperative Study - Clinical Global Impression of Change (ADCS-CGIC)
0; 0; 0; 0; 2; 0
SECONDARY
ADCS - Activities of Daily Living (ADCS-ADL)
62.7; 60.7; 63.3; 62.8; 61.2; 62.0
SECONDARY
Movement Disorder Society - United Parkinson's Disease Rating Scale Part III (MDS-UPDRS Part III)
29.2; 25.4; 28.1; 28.7; 23.3; 28.7
SECONDARY
Change From Baseline in the Power of Attention Composite Score of the Cognitive Drug Research (CDR) System Battery
119.89; 620.82; 279.62
SECONDARY
Neuropsychiatric Inventory (NPI-12) - Domain: Total Score A-L (Frequency x Severity)
12.0; 13.8; 10.0; 9.8; 10.5; 7.9

Summary

Multi-center, randomized, double-blind, placebo-controlled, 6- month study in subjects with mild to moderate Dementia with Lewy Bodies.

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

  • 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)
  • 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.
  • 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.).
  • 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.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05225415). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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