Multiple Dose Safety Study of NPT088 in Patients With Mild to Moderate Probable Alzheimer's Disease

This study is a multicenter Phase 1, randomized, double-blind, placebo-controlled,
multiple-dose, dose-escalation safety and tolerability study of NPT088 or placebo in patients
with Probable AD with a MMSE score of 16-27. Enrolled patients will receive an intravenous
infusion of NPT088 or placebo once a month for six months during this study. Four dose
cohorts are planned with the first two cohorts enrolling 9 patients each (6 NPT088: 3
placebo) and the final two cohorts enrolling 24 patients each (16 NPT088: 8 placebo) for a
total of 66 patients (44 NPT088: 22 placebo).

Inclusion Criteria: For enrollment in the study, participants must

- be between 50 and 85 years of age, inclusive

- have a Mini Mental State Examination (MMSE) scores between 16-27 (inclusive)

- have a Modified Hachinski Score of less than or equal to 4

- have a diagnosis of Probable Alzheimer's Disease (AD) according to consensus criteria
defined by the National Institute on Aging-Alzheimer's Association work group

- have a Clinical Dementia Rating Scale (CDR) of 0.5 or 1.0, with the memory box score
equal to or greater than 0.5

- have a positive florbetapir positron emission tomography (PET) amyloid scan

- consent to apolipoprotein E (ApoE) genotyping

- be willing to undergo repeat Magnetic Resonance Imaging (MRI) and PET imaging

- be on stable doses of allowed medications for at least 30 days prior to Screening.
Concurrent treatment with cholinesterase inhibitors and/or memantine is allowed

- be in good healthy apart from the clinical diagnosis of AD

- have a dedicated Caregiver who provides care at least 4 hours a day for 4 days a week
and will provide informed consent for their participation

Exclusion Criteria: For enrollment in the study, participants must NOT:

- have a history of, or screening MRI indicative of any significant brain abnormality

- have any major medical illness or unstable medical condition or in the opinion of the
Investigator have any reason that may interfere with the participants ability to
comply with the study procedures and abide by study restrictions or with the ability
to interpret safety data

- reside in a nursing home or need 24-hour care and supervision

- take excluded medications

- have exclusionary values on the Screening blood and urine sample

- have been treated with immunomodulators to treat AD

- have participated in an investigational drug or device study within 90 days

- have a known allergy to study drug