← Trials/Trial dossier/NCT05004987
Aβ Dynamics in LLMD
Depression Treatment and Aβ Dynamics: A Study of Alzheimer's Disease Risk (ABD Study)
Lead sponsor
Asset
Escitalopram
Listed sites
2
Recruiting sites
2
Enrollment
60
estimated
Study population
Alzheimer’s disease
Key I/E criterion
•MMSE ≥27
Primary endpoints
•Cerebrospinal Fluid (CSF) Aβ40 Biomarker Levels•Cerebrospinal Fluid (CSF) Aβ42 Biomarker Levels•Vascular Dysfunction (VD) Biomarker Levels
Footprint
Where this trial recruits
Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.
Identifiers
Registered as
Timeline
Milestones
Assets
Drug assets
Study populations
Who this study enrolls
Eligibility
Who can enroll
Inclusion criteria
1. Male and female subjects, age 60+ years inclusive, at the time of signing the informed consent.
2. Meeting Structured Clinical Interview (SCID-5-RV) for DSM-5 criteria for Major depressive disorder.
3. Montgomery-Åsberg Depression Rating Scale (MADRS) ≥18.
4. Have results of a physical examination, neurological examination, vitals, and EKG within normal limits at screening.
5. Cognitively unimpaired at screening visit as defined by Mini-Mental State Examination (MMSE) >27.
6. Clinical Dementia Rating Scale (CDR) Global of 0*.
7. A score of 85 or greater on the RBANS delayed memory index score.
8. Fluent in English, because some of the instruments used in this study have not been translated and validated in other languages, and are able to read at a 6th grade level or equivalent, as determined by the PI.
9. Medically stable with no significant cerebrovascular, neurological, or systemic disease expected to interfere with the study.
10. Adequate auditory acuity and normal-to-corrected vision.
11. Willing to undergo brain MRI, urine drug screen and blood sampling for routine laboratory testing, lumbar puncture, APOE genotyping and plasma drug levels.
12. Only individuals with normal or non-clinically significant abnormalities on routine laboratory tests, will be included.
Exclusion criteria
1. History of brain tumor, MRI evidence of brain damage or brain disease including significant trauma, hydrocephalus, seizures, or confluent (or more extensive) white matter hyperintensities.
2. Mental retardation, or other serious neurological disorder (e.g. Parkinson's disease or other movement disorders).
3. Subjects with a Fazekas scale >2.
4. Significant history of alcoholism or drug abuse in the past 2 years. Fulfilling SCID-5-RV/DSM-5 criteria for current or past diagnosis of any psychiatric disorder (e.g., schizophrenia, bipolar disorder, or any psychotic disorder) other than recurrent MDD or anxiety disorders (e.g., panic disorder, agoraphobia, etc.).
5. A current significant risk for suicidality based on the Columbia-Suicide-Severity Rating Scale (C-SSRS).
6. Insulin dependent diabetes.
7. Evidence of clinically relevant or unstable cardiac, pulmonary, endocrine or hematological conditions.
8. Any prosthetic devices (e.g., pacemaker or surgical clips) that constitutes a hazard for MRI imaging.
9. Positive urine drug screen for illicit drugs.
10. History of poor tolerance to, poor response to, or ongoing treatment with escitalopram.
11. If taking antidepressants, currently taking fluoxetine, due to the length of time required to washout.
12. Treatment with following medications will not be permitted. In some cases, medications will be allowed if medically prescribed and dose regimen stable. Note: Some medications (e.g., amphetamines, opiates) may appear on the routine urine drug test in the screening period but can be allowed as per protocol.
Endpoints (7)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Coverage by outcome category
Behavior / neuropsychiatric
1 endpointChange in Scores on Montgomery-Asberg Depression Ration Scale (MADRS)
Time frame:Baseline, Week 8
change from baseline, improvement
Amyloid biomarkers
2 endpointsChange in Cerebrospinal Fluid (CSF) Aβ40 Biomarker Levels
Time frame:Baseline, Week 8
change from baseline, improvement
Change in Cerebrospinal Fluid (CSF) Aβ42 Biomarker Levels
Time frame:Baseline, Week 8
change from baseline, improvement
Tau biomarkers
2 endpointsChange in Cerebrospinal Fluid (CSF) P-tau Biomarker Levels
Time frame:Baseline, Week 8
change from baseline, improvement
Change in Cerebrospinal Fluid (CSF) T-tau Biomarker Levels
Time frame:Baseline, Week 8
change from baseline, improvement
Other (unclassified)
2 endpointsChange in Vascular Dysfunction (VD) Biomarker Levels
Time frame:Baseline, Week 8
change from baseline, improvement
Change in Plasma Aβ Biomarker Levels
Time frame:Baseline, Week 8
change from baseline, improvement
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 21, 2026 snapshot.