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RecruitingPhase 4

Aβ Dynamics in LLMD

Depression Treatment and Aβ Dynamics: A Study of Alzheimer's Disease Risk (ABD Study)

Lead sponsor

NYU Langone Health

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 LevelsCerebrospinal Fluid (CSF) Aβ42 Biomarker LevelsVascular 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

Org study ID21-00535
NCT IDNCT05004987

Timeline

Milestones

Study first posted2021-08-13actual
Study start2022-02-04actual
Last update posted2026-05-06actual
Primary completion2026-12-31estimated
Study completion2027-06-30estimated

Assets

Drug assets

Study populations

Who this study enrolls

Alzheimer’s disease

Eligibility

Who can enroll

Minimum age60 Years
SexAll
Healthy volunteersNot accepted

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.

-If study partner is not available, the CDR will be skipped

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.

-For subjects taking prescribed psychoactive medications and supplements (i.e., opioids, amphetamines, amphetamine-like substances, and cannabinoids), must be on a stable dose for 1 month prior to randomization.
-Anti-Parkinsonian medications (carbidopa/levodopa, amantadine, bromocriptine, pergolide, selegiline).
-Cholinesterase inhibitors and memantine
-Continuous aspirin (any dosage) use which can affect platelet function is prohibited. Exception: If participant is on low dose aspirin for prophylaxis and is willing to temporarily discontinue prior to research blood draw (i.e., 2 days before).
-Continuous use of other medications which are also known to affect platelet function, including nonsteroidal anti-inflammatory drugs (NSAIDs), anti-histamines. Exception: If participant is taking medication continuously and is willing to temporarily discontinue prior to research blood draw (i.e., 2 days before)

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

Amyloid biomarkers
2
Tau biomarkers
2
Other (unclassified)
2
Behavior / neuropsychiatric
1

Behavior / neuropsychiatric

1 endpoint
Primary/protocol endpoint

Change in Scores on Montgomery-Asberg Depression Ration Scale (MADRS)

Time frame:Baseline, Week 8

change from baseline, improvement

Amyloid biomarkers

2 endpoints
Primary/protocol endpoint

Change in Cerebrospinal Fluid (CSF) Aβ40 Biomarker Levels

Time frame:Baseline, Week 8

change from baseline, improvement

Primary/protocol endpoint

Change in Cerebrospinal Fluid (CSF) Aβ42 Biomarker Levels

Time frame:Baseline, Week 8

change from baseline, improvement

Tau biomarkers

2 endpoints
Other/protocol endpoint

Change in Cerebrospinal Fluid (CSF) P-tau Biomarker Levels

Time frame:Baseline, Week 8

change from baseline, improvement

Other/protocol endpoint

Change in Cerebrospinal Fluid (CSF) T-tau Biomarker Levels

Time frame:Baseline, Week 8

change from baseline, improvement

Other (unclassified)

2 endpoints
Primary/protocol endpoint/low confidence

Change in Vascular Dysfunction (VD) Biomarker Levels

Time frame:Baseline, Week 8

change from baseline, improvement

Other/protocol endpoint/low confidence

Change in Plasma Aβ Biomarker Levels

Time frame:Baseline, Week 8

change from baseline, improvement

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 21, 2026
Endpoint classificationDelfa ADRD endpoint taxonomy
Results tableno registry results posted yet

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.