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

Participating center: A single-center trial performed at Hadassah - Hebrew University Medical Center in Jerusalem, Israel. The investigators have vast experience in performing full medical and neuropsychological evaluations, and in performing clinical trials in patients with cognitive decline. Patients will be recruited via the cognitive Neurology clinics at the Hadassah Ein-Kerem campus, Hadassah Mount Scopus campus, and Merhav out-patient clinic for cognitive Neurology, which is associated and operated by Hadassah Neurologists.

Patient recruitment: 50 patients with mild cognitive impairment (MCI) will be recruited, according to its accepted definition. Patients with MCI will undergo standard evaluation, including brain imaging (MRI / CT), thyroid function tests, Vitamin B12, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP) to rule out other causes of cognitive decline.

The investigators expect that approximately 70% of recruited patients will display increased plasma p-tau217 level, indicating MCI of Alzheimer's type.

Clinical and neuropsychological evaluation will include: (1) Full demographic data (age, gender, education level and occupation, family status, ethnicity and country of origin); (2) Clinical data on risk factors (metabolic/ cardiovascular risk factors - heart disease, diabetes, hypertension, hyperlipidemia; Infectious/ inflammatory risk factors - periodontal disease, systemic infections, systemic inflammatory conditions; Lifestyle factors - smoking, alcohol consumption, sleeping disorder, physical activity; and Mental factors - anxiety and depression, cognitive activity); (3) MoCA (in Hebrew version); (4) Mild Behavioral Impairment checklist (MBI-C), or Neuropsychiatric Inventory (NPI) questionnaire (in Hebrew version); (5) ADL and iADL questionnaire; (6)Trail making test -B (TMT-B); Word fluency test.

Determination of blood biomarkers: Venous blood will be drawn upon recruitment in a tube containing EDTA to prevent clotting. The blood will be centrifuged at 1200 rpm for 5 minutes, and plasma stored in -80°C, within two hours of drawing the blood sample. The samples will be stored in a temperature-controlled and monitored freezer, until delivery in dry ice to the central lab (Prof. Ben-Hur's lab at the Ein-Kerem campus) for determination of biomarkers. Blood samples that were collected at recruitment will be tested for p-tau217 level, neurofilament light and GFAP. The baseline p-tau217 will serve as a reference value for monitoring individual response to therapy, as well as the group trend in the other biomarkers.

Treatment: All patients will receive Cerebonin (Egb761) 240mg per day, by tablets of 120mg, taken twice daily.

Follow-up: After initiation of treatment, patients will be invited for follow-up visits at 3 months and 6 months. Clinical data (risk factor assessment), MoCA, MBI-C, iADL and plasma p-tau217 level will be evaluated in each visit. The investigators will evaluate total MoCA score, as well as its breakdown into cognitive domains (attention, executive, memory (both free and cued / recognition recall), visuospatial, language, and orientation). One point is added if the subject has ≤12 years of education.

Evaluating response to therapy: (1) In patients with high baseline plasma p-tau181 level, the investigators will compare pre- and post-treatment plasma p-tau-217 levels (Δp-tau). Since plasma p-tau217 is considered a biomarker of active brain disease, a reduction in its level will suggest a disease-modifying therapeutic effect; (2) The investigators will examine the trend in group averages of neurofilament and GFAP, as additional disease biomarkers. (3) The investigators will determine the symptomatic clinical response according to improvement in MoCA, MBI-C/NPI, TMT-B and ADL/iADL scores after 3 and 6 months of treatment; (4) The investigators will compare the treatment effect in MCI patients with high- versus normal- plasma p-tau217 levels (eg. in MCI of AD type versus non-AD type); (5) The investigators will examine the association between clinical improvement and change in the plasma level of biomarkers.

• Symptomatic effect [Time frame: The test will be performed at recruitment, at 3- and 6-months of treatment]
• Symptomatic effect [Time frame: The test will be performed at recruitment, at 3- and 6-months of treatment]
• Symptomatic effect [Time frame: The test will be performed at recruitment, at 3- and 6-months of treatment]
• Symptomatic effect [Time frame: The test will be performed at recruitment, at 3- and 6-months of treatment]
• Change in plasma GFAP level [Time frame: Plasma biomarker will be determined at recruitment and at 3- and 6-months]
• Change in plasma neurofilament-light level [Time frame: Plasma biomarker will be determined at recruitment and at 3- and 6-months]