Study in Subjects With Mild-to-Moderate Alzheimer's Dementia

Running, not enrolling · Phase 1/Phase 2 · Has a placebo group

Conditions studied: Alzheimer Disease

In brief

ALZN002-01 is a first-in-human, randomized, double-blind, placebo-controlled, parallel-group, phase 1/2a study of autologous amyloid beta mutant peptide-pulsed dendritic cells (ALZN002) in subjects with mild-to-moderate dementia of the Alzheimer's type.

Key facts

Study ID

NCT05834296

Run by

Alzamend Neuro, Inc.

People needed

30

Starts

2023-07-05

Expected to finish

2028-03-03

Last updated by the study team

2025-09-02

Who can join

Age: 60 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Potential study subjects must satisfy the following criteria to be randomized in the study:
• Age ≥60 and ≤85 years with no restrictions on gender, race, or ethnicity.
• Able and willing to give informed consent and adhere to study requirements, including testing for cognitive and functional abilities.
• Confirmation of AD at Screening based either on a positive amyloid PET obtained at Screening or based on historical positive amyloid PET taken within 6 months prior to the screening visit consistent with AD. If historical amyloid PET imaging is used for inclusion
• there should be no clinically significant change in the subject's symptoms and cognitive abilities within the 6 months prior to Screening.
• The quality and accuracy of the historical positive amyloid PET needs to be confirmed by the central imaging center
• Willing and able to have amyloid PET taken at Screening (if no historical adequate amyloid PET within 6 months of Screening is available) to confirm AD and at Week 31 and Week 143 as a potential efficacy measure.
• Willing and able to have magnetic resonance imaging (MRI) taken at Screening, at 1 year (Week 55) and 2 years (Week 101) after the 3rd dose, and at 1 year after the 10th dose (Week 143/EOS) as potential safety measures.
• Males (non-vasectomized and vasectomized) must agree to use barrier contraception during the study until 30 days after the last dose of the study investigational treatment.
• Females must meet one the of the following criteria:
• a. Either is of childbearing potential and agrees to use an acceptable contraceptive method. Acceptable contraceptive methods include:
• i. Abstinence from heterosexual intercourse from the Screening visit through to at least 30 days after the last dose of the study investigational treatment
• ii. One of the following highly-effective contraceptive methods, used from at least 28 days prior to the Screening visit through to at least 30 days after the last dose of the study investigational treatment:
• Systemic contraceptive (combined birth control pills, injectable/implant/insertable hormonal birth control products, or transdermal patch)
• Intrauterine device (with or without hormones)
• Male condom used with male partner vasectomized at least 6 months prior to the Screening visit
• iii. One of the following double-barrier contraceptive methods, used from the Screening visit through to at least 30 days after the last dose of the study investigational treatment:
• Male condom used simultaneously with diaphragm plus spermicide
• Male condom used simultaneously with cervical cap plus spermicide
• Or
• b. Is of non-childbearing potential, defined as surgically sterile (ie, has undergone complete hysterectomy, bilateral oophorectomy, or tubal ligation), or is in a postmenopausal state (ie, at least 1 year without menses, not attributable to another cause, prior to the Screening visit)
• In the event that the subject requires a study partner, he/she must be reliable and will provide written informed consent to participate and be in frequent contact with the participant. The study partner must be familiar with the subject's overall function and behavior, such as day-to-day activities and cognitive abilities.
• Able to speak, read, and write (for cognitive testing).
• Clinical diagnosis of probable or possible AD based on National Institute on Aging - Alzheimer's Association (NIA-AA) criteria by a qualified clinician.
• Clinical diagnosis of at least mild dementia according to the CDR Global Score of 0.5 to 2 at screening and Baseline

You may not qualify if…

• Subjects who meet any of the following criteria will be excluded from participating in the study:
• Prior immunotherapies and specifically therapies that may elicit T cell or antibody responses to Aβ, whether investigational or approved by the FDA, for AD or other conditions.
• Central nervous system-related exclusions:
• Delirium, non-AD dementia or cognitive impairment, or other encephalopathies.
• Subjects with major psychiatric disorder such as schizophrenia, bipolar disorder or major depressive disorder, or has current alcohol or substance abuse based on psychiatric consultation at Screening visit.
• Neuropsychiatric Inventory (NPI-Q) total score ≥14 or score ≥4 in any NPI domain (clinically significant neuropsychiatric symptoms). Apathy score ≥4 acceptable.
• At risk for suicide in the opinion of the investigator or the subject answers "yes" to "Suicidal Ideation" Item 4 or 5 on the Columbia-Suicide Severity Rating Scale (C-SSRS) (at the time of evaluation) at the screening visit or attempted suicide within the last 2 years.
• Modified Hachinski Scale10 score >4 or evidence of stroke within the past 5 years.
• Neuroimaging exclusions by history or entry criteria: Arteriovenous malformation, brain mass, suggestive changes of cerebral amyloid angiopathy (CAA), aneurysms, or other changes that increase risk of hemorrhage, multiple cerebral macrohemorrhages, or other cerebrovascular complications as deemed by the Principal Investigator and/or the Safety Adjudication Committee that might account for cognitive symptoms.
• MRI-related exclusion criteria: >4 lacunar infract, Grade III white matter hyperintensities (Fazekas scale), intracranial mass, evidence of normal pressure hydrocephalus or other anatomical findings that might affect safety or causes of cognitive impairments, and any contraindications for MRI scanning, including implanted metallic devices (eg, non MRI safe cardiac pacemaker or neurostimulator; some artificial joints; metal pins; surgical clips; or other implanted metal parts), or claustrophobia or discomfort in confined spaces.
• History of moderate or more severe traumatic brain injury in the 2 years prior to signing the consent to participate in the study.
• History of brain tumor, subdural hematoma, or other clinically significant (in the judgment of the investigator) space-occupying lesion on MRI.
• History of seizure disorder.
• Contraindications for PET scanning or any protocol testing procedure.
• Systemic related exclusions:
• Known autoimmune disease (properly treated hypothyroidism and stable rheumatoid arthritis allowed), biomarkers exceeding 1:80 for antinuclear antibodies, 20 IU/mL (or 1:80) for rheumatic factor, 26 AU/mL for antineutrophil cytoplasmic antibodies; or history of allergic reaction to any related product of infused cells.
• Current malignancy, with the exception of non-invasive (stage 0 or stage 1) basal and squamous cell carcinoma with planned excision. Subjects with a prior successfully treated malignancy and a sufficient follow-up to exclude the likelihood of recurrence may be enrolled at the discretion of the Principal Investigator.
• History of or current HIV, HBV, or HCV (unless subjects who test positive for hepatitis C antibody are in remission with sustained virologic response, as evidenced by undetectable HCV RNA level using a sensitive assay ≥12 weeks after completion of HCV therapy).
• Elevated C-reactive protein (>5.0 mg/L) using a high sensitivity test.
• Fever, signs or symptoms of active illness or infection, or a diagnosed infectious disease.
• Immunizations within 4 weeks of the leukapheresis or investigational treatment (ALZN002 or placebo) administrations.
• Recent (past 8 weeks) donation of blood or loss of blood (>400 cc).
• Insulin-dependent diabetes mellitus
• The following medications are excluded with the noted exceptions:
• Initiation of cholinesterase inhibitors, memantine HCl, or other drugs for the treatment of cognitive loss within 60 days of Screening, unless the dose is stable for >60 days prior to Screening and is expected to remain stable throughout the study participation

Where it is running

• First Excellent Research Group — Doral, Florida, United States

Full record on ClinicalTrials.gov

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