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NCT07392723 · ClinicalTrials.gov registry record · Phase 2

ALA-enriched Nutrition for Prevention of Cognitive Decline in APOE4 Older Adults

A Phase 2 study of Alzheimer Disease and Cognitive Dysfunction, sponsored by Michal Schnaider Beeri, Ph.D..

Recruiting
Registry status
Phase 2
Development phase
20
Enrollment target
1
Study location

NCT07392723: Recruiting Phase 2 study of Alzheimer Disease and Cognitive Dysfunction, sponsored by Michal Schnaider Beeri, Ph.D..

NCT07392723 is a Phase 2 study of Alzheimer Disease and Cognitive Dysfunction that is actively recruiting participants, run by Michal Schnaider Beeri, Ph.D.. The registered enrollment target is 20 participants, below the 2,751-participant average among 306 other Alzheimer Disease trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07392723, a Phase 2 study of Alzheimer Disease and Cognitive Dysfunction, is actively recruiting participants, sponsored by Michal Schnaider Beeri, Ph.D..

RECRUITING
Registry status
Phase 2
Development phase
20 participants
Enrollment target
1
Study location

Study Summary

This randomized, double-blind, placebo-controlled pilot trial will evaluate the effects of alpha-linolenic acid (ALA) supplementation on cognitive function, blood-brain barrier integrity, and brain vascular health in older adults with mild cognitive impairment and APOE4 genotype. By targeting the endogenous synthesis of docosahexaenoic acid (DHA) through ALA supplementation, the investigators aim to overcome the limitations of direct DHA supplementation, particularly in APOE4 carriers who exhibit low brain DHA levels and impaired blood-brain barrier function. This innovative approach offers a safe, cost-effective, and easily implementable therapeutic strategy for older adults at high risk for Alzheimer's dementia, especially APOE4 carriers, addressing a critical need given the limited cognitive benefits and significant adverse events of current amyloid-clearing drugs in this population.

Primary Outcome

Change in global cognition score from baseline to 6 months measured by an average of the z-scores across a broad cognitive battery, will be compared between ALA and placebo groups.

Interventions

  • DRUG Alpha-Linolenic Acid (2.6 g/day)
  • DIETARY_SUPPLEMENT Placebo Control Group

Study Locations (1)

New Jersey

  • Rutgers - Institute for Health - New Brunswick

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2025-01-12
Est. Completion 2027-10
Phase Phase 2
Michal Schnaider Beeri, Ph.D.

1 total trials

What NCT07392723 shows while recruiting

NCT07392723 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 2,751-participant average among 306 other Alzheimer Disease trials with a reported enrollment target (99% lower).

The record links to 6 conditions, with Alzheimer Disease appearing as the primary indexed condition, and to 2 interventions - of which Alpha-Linolenic Acid (2.6 g/day) is the first listed.

NCT07392723 reports a single indexed study location in New Jersey.

Frequently Asked Questions

What is clinical trial NCT07392723 about?

NCT07392723 is a clinical study titled "ALA-enriched Nutrition for Prevention of Cognitive Decline in APOE4 Older Adults". This randomized, double-blind, placebo-controlled pilot trial will evaluate the effects of alpha-linolenic acid (ALA) supplementation on cognitive function, blood-brain barrier integrity, and brain vascular health in older adults with mild cognitive impairment and APOE4 genotype. By targeting the en...

What is the current status of trial NCT07392723?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2025-01-12. Estimated completion is 2027-10.

What conditions does trial NCT07392723 study?

This clinical trial studies the following conditions: Alzheimer Disease, Cognitive Dysfunction, Brain Aging, Blood-Brain Barrier, Apolipoprotein E, Deficiency or Defect of.

What interventions are being tested in trial NCT07392723?

The interventions under investigation include: Alpha-Linolenic Acid (2.6 g/day) (DRUG), Placebo Control Group (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT07392723?

This trial is sponsored by Michal Schnaider Beeri, Ph.D., which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07392723 being conducted?

This trial has 1 study location across New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Alzheimer Disease

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07392723's enrollment target sits among peer trials

20 264th of 306 higher than 32 of 306 other Alzheimer Disease trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Alzheimer Disease trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07392723, the US trial registry maintained by the National Library of Medicine. NCT07392723 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.