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Aβ Dynamics in LLMD

Primary Purpose

Alzheimer Disease, Major Depressive Disorder

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Escitalopram Oxalate
Placebo
Sponsored by
NYU Langone Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alzheimer Disease

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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. Have a reliable and competent study partner who can accompany the subject to the Screening Visit to verify absence of impairment in cognitive functions or activities of daily living.
  12. Willing to undergo brain MRI, urine drug screen and blood sampling for routine laboratory testing, lumbar puncture, APOE genotyping and plasma drug levels.
  13. Only individuals with normal hepatic and renal function including normal creatinine clearance 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 other than recurrent MDD including schizophrenia, bipolar disorder, dysthymic disorder, panic disorder, agoraphobia, specific phobia, social phobia, obsessive compulsive disorder, post-traumatic disorder, or any psychotic disorder.
  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. Currently taking medications potentially affecting cognition other than SSRIs; narcotic analgesics,chronic use of medications with anticholinergic activity, Anti-Parkinsonian medications (carbidopa/levodopa, amantadine, bromocriptine, pergolide, selegiline).

    • Others medications that are exclusionary include: amphetamines, amphetamine-like compounds, appetite suppressants, phenothiazines, reserpine, buspirone, clonidine, disulfiram, guanethidine, theophylline, melatonin, salicylates, cholinesterase inhibitors and memantine. Continuous aspirin (any dosage) use and St. John's Wort are excluded.
    • For subjects taking antidepressants at screening, no dosage changes for ≥3 months.

Sites / Locations

  • NYU Langone HealthRecruiting
  • Nathan S. Kline Institute for Psychiatric ResearchRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Escitalopram (ESC)

Placebo (PBO)

Arm Description

Outcomes

Primary Outcome Measures

Change in Cerebrospinal Fluid (CSF) Aβ40 Biomarker Levels
Change in Cerebrospinal Fluid (CSF) Aβ42 Biomarker Levels
Change in Vascular Dysfunction (VD) Biomarker Levels
Change in Scores on Montgomery-Asberg Depression Ration Scale (MADRS)
MADRS consists of 10 items evaluating core symptoms of depression (e.g, apparent sadness, reported sadness, inner tension, reduced sleep, reduced appetite, concentration difficulties, lassitude, inability to feel, pessimistic thought, and suicidal thoughts). Each symptom is rated on a 0-6 scale (0=no abnormality, 6=severe). The total score ranges from 0 to 60; the higher the score, the more severe the symptoms.

Secondary Outcome Measures

Full Information

First Posted
August 12, 2021
Last Updated
December 29, 2022
Sponsor
NYU Langone Health
Collaborators
National Institute on Aging (NIA)
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1. Study Identification

Unique Protocol Identification Number
NCT05004987
Brief Title
Aβ Dynamics in LLMD
Official Title
Depression Treatment and Aβ Dynamics: A Study of Alzheimer's Disease Risk (ABD Study)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 4, 2022 (Actual)
Primary Completion Date
April 2026 (Anticipated)
Study Completion Date
June 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NYU Langone Health
Collaborators
National Institute on Aging (NIA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will examine the biological factors that may modulate the relationship between depression and the development of Alzheimer's disease (AD). Since the direction of causation between depression and the biological factors associated with AD is unknown, the only way to understand cause and associated risk is to treat the depressive symptoms and examine the effects on AD biomarkers. The study involves an FDA-approved treatment for major depressive disorder. It will compare the SSRI antidepressant escitalopram with placebo. The hypothesis is that a reduction in depressive symptoms will be associated with a normalization of CSF AD biomarkers as well as peripheral inflammatory markers. This research would contribute to fundamental knowledge about potentially modifiable risks of Alzheimer's disease (AD).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer Disease, Major Depressive Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Masking Description
Both the study staff and the subjects will be blind to the study assignment.
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Escitalopram (ESC)
Arm Type
Active Comparator
Arm Title
Placebo (PBO)
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Escitalopram Oxalate
Other Intervention Name(s)
Lexapro, ESC
Intervention Description
The daily dose of ESC/PBO will be 10 mg for the first 2 weeks, then increase to 20 mg as tolerated, with an option to reduce back to 10 mg if necessary.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
PBO
Intervention Description
Daily dose of placebo will mimic that of ESC.
Primary Outcome Measure Information:
Title
Change in Cerebrospinal Fluid (CSF) Aβ40 Biomarker Levels
Time Frame
Baseline, Week 8
Title
Change in Cerebrospinal Fluid (CSF) Aβ42 Biomarker Levels
Time Frame
Baseline, Week 8
Title
Change in Vascular Dysfunction (VD) Biomarker Levels
Time Frame
Baseline, Week 8
Title
Change in Scores on Montgomery-Asberg Depression Ration Scale (MADRS)
Description
MADRS consists of 10 items evaluating core symptoms of depression (e.g, apparent sadness, reported sadness, inner tension, reduced sleep, reduced appetite, concentration difficulties, lassitude, inability to feel, pessimistic thought, and suicidal thoughts). Each symptom is rated on a 0-6 scale (0=no abnormality, 6=severe). The total score ranges from 0 to 60; the higher the score, the more severe the symptoms.
Time Frame
Baseline, Week 8
Other Pre-specified Outcome Measures:
Title
Change in Plasma Aβ Biomarker Levels
Time Frame
Baseline, Week 8
Title
Change in Cerebrospinal Fluid (CSF) P-tau Biomarker Levels
Time Frame
Baseline, Week 8
Title
Change in Cerebrospinal Fluid (CSF) T-tau Biomarker Levels
Time Frame
Baseline, Week 8

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male and female subjects, age 60+ years inclusive, at the time of signing the informed consent. Meeting Structured Clinical Interview (SCID-5-RV) for DSM-5 criteria for Major depressive disorder. Montgomery-Åsberg Depression Rating Scale (MADRS) ≥18. Have results of a physical examination, neurological examination, vitals, and EKG within normal limits at screening. Cognitively unimpaired at screening visit as defined by Mini-Mental State Examination (MMSE) >27. Clinical Dementia Rating Scale (CDR) Global of 0. A score of 85 or greater on the RBANS delayed memory index score. 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. Medically stable with no significant cerebrovascular, neurological, or systemic disease expected to interfere with the study. Adequate auditory acuity and normal-to-corrected vision. Have a reliable and competent study partner who can accompany the subject to the Screening Visit to verify absence of impairment in cognitive functions or activities of daily living. Willing to undergo brain MRI, urine drug screen and blood sampling for routine laboratory testing, lumbar puncture, APOE genotyping and plasma drug levels. Only individuals with normal hepatic and renal function including normal creatinine clearance will be included. Exclusion Criteria: 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. Mental retardation, or other serious neurological disorder (e.g. Parkinson's disease or other movement disorders). Subjects with a Fazekas scale >2. 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 other than recurrent MDD including schizophrenia, bipolar disorder, dysthymic disorder, panic disorder, agoraphobia, specific phobia, social phobia, obsessive compulsive disorder, post-traumatic disorder, or any psychotic disorder. A current significant risk for suicidality based on the Columbia-Suicide-Severity Rating Scale (C-SSRS). Insulin dependent diabetes. Evidence of clinically relevant or unstable cardiac, pulmonary, endocrine or hematological conditions. Any prosthetic devices (e.g., pacemaker or surgical clips) that constitutes a hazard for MRI imaging. Positive urine drug screen for illicit drugs. History of poor tolerance to, poor response to, or ongoing treatment with escitalopram. If taking antidepressants, currently taking fluoxetine, due to the length of time required to washout. Currently taking medications potentially affecting cognition other than SSRIs; narcotic analgesics,chronic use of medications with anticholinergic activity, Anti-Parkinsonian medications (carbidopa/levodopa, amantadine, bromocriptine, pergolide, selegiline). Others medications that are exclusionary include: amphetamines, amphetamine-like compounds, appetite suppressants, phenothiazines, reserpine, buspirone, clonidine, disulfiram, guanethidine, theophylline, melatonin, salicylates, cholinesterase inhibitors and memantine. Continuous aspirin (any dosage) use and St. John's Wort are excluded. For subjects taking antidepressants at screening, no dosage changes for ≥3 months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Antero Sarreal, MD
Phone
845-398-6532
Email
Antero.sarreal@nki.rfmh.org
First Name & Middle Initial & Last Name or Official Title & Degree
Chelsea Reichert Plaska, PhD
Phone
845-398-5583
Email
Chelsea.reichert@nki.rfmh.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nunzio Pomara, MD
Organizational Affiliation
NYU Langone Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
NYU Langone Health
City
New York
State/Province
New York
ZIP/Postal Code
10016
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nunzio Pomara, MD
Facility Name
Nathan S. Kline Institute for Psychiatric Research
City
Orangeburg
State/Province
New York
ZIP/Postal Code
10962
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Antero Sarreal, MD
Phone
845-398-6532
Email
Antero.sarreal@nki.rfmh.org
First Name & Middle Initial & Last Name & Degree
Nunzio Pomara, MD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data that underlie the results reported in this article, after deidentification (text, tables, figures, and appendices) will be shared upon reasonable request.
IPD Sharing Time Frame
Beginning 9 months and ending 36 months following article publication or as required by a condition of awards and agreements supporting the research.
IPD Sharing Access Criteria
The investigator who proposed to use the data will have access to the data upon reasonable request. Requests should be directed to nunzio.pomara@nki.rfmh.org. To gain access, data requestors will need to sign a data access agreement.

Learn more about this trial

Aβ Dynamics in LLMD

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