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Clinical Trials in Israel / NCT07287852
Enrolling by invitation Phase 2

A Pilot Study to Examine the Effect of Egb761 on Plasma Biomarker Levels and on Cognitive Function in Patients With MCI

NCT07287852 · tracked via the Priya Life Science Israel tracker
Phase
Phase 2
Started
2024-08-20
Last updated
2025-12-17

Condition(s) studied

Alzheimer Disease (AD)Mild Cognitive Impairment (MCI)

Investigational drug(s) / intervention(s)

Ginkgo Biloba Extract 761

Ginkgo Biloba Extract 761: Each participant will receive two 120mg Egb761 pills per day along the 6 month trial

Study summary

The goal of this clinical trial is to learn if the drug Egb761, produced from Ginkgo Biloba extract, works to improve the blood level of a biomarker of Alzheimer's disease, called phosphorylated-tau217 (p-tau217), which serves as a biomarker for disease activity in the brain. The main questions it aims to answer are:

Does drug Egb761 lower the plasma level of p-tau217 in patients with mild cognitive impairment? Does drug Egb761 improve cognitive and behavioral functions in these patients? Does Egb761 affect the blood levels of neurofilament-light (Nfl) and glial-fibrillary-acidic-protein (GFAP), which serve as additional biomarkers for brain disease activity?

Participants will:

Take Egb761 twice daily for 6 months Visit the clinic once every 3 months for checkups and tests Keep a diary of their symptoms

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Mild cognitive impairment, as defined by MoCA score of 19-25. * Preserved instrumental activities of daily life (iADL). * Clinical impression of MCI of AD type, and lack of major medical and neurological conditions, as detailed in the exclusion criteria. Exclusion Criteria: * Extrapyramidal signs, existence of multi-infract dementia, or Fronto-Temporal dementia, according to clinical impression by treating cognitive Neurologist. * Active cancer, severe cardio-pulmonary disease or other medical condition which negatively affects ability to evaluate patients and complete follow-up. * Inability to sign an informed consent due to psychiatric or dementing condition. * Hypersensitivity to any ingredient of the study medication.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hadassah medical Center Jerusalem Israel

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07287852 on ClinicalTrials.gov ↗ ← All trials in Israel