| Eligibility |
Inclusion Criteria:
Potential study subjects must satisfy the following criteria to be randomized in the study:
1. Age =60 and =85 years with no restrictions on gender, race, or ethnicity.
2. Able and willing to give informed consent and adhere to study requirements, including
testing for cognitive and functional abilities.
3. 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
1. there should be no clinically significant change in the subject's symptoms and
cognitive abilities within the 6 months prior to Screening.
2. The quality and accuracy of the historical positive amyloid PET needs to be
confirmed by the central imaging center
4. 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.
5. 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.
6. 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.
7. 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)
8. 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.
9. Able to speak, read, and write (for cognitive testing).
10. Clinical diagnosis of probable or possible AD based on National Institute on Aging -
Alzheimer's Association (NIA-AA) criteria by a qualified clinician.
11. Clinical diagnosis of at least mild dementia according to the CDR Global Score of 0.5
to 2 at screening and Baseline
12. Mini-Mental State Examination (MMSE) score of 14 - 26 and ADAS-cog11 score greater
than 12 at screening and Baseline.
13. Willing and able to undergo leukapheresis as needed.
14. Consent to undergo d HLA geno-typing and PaxGene RNA.
Exclusion Criteria:
Subjects who meet any of the following criteria will be excluded from participating in the
study:
1. Prior immunotherapies and specifically therapies that may elicit T cell or antibody
responses to Aß, whether investigational or approved by the FDA, for AD or other
conditions.
2. Central nervous system-related exclusions:
1. Delirium, non-AD dementia or cognitive impairment, or other encephalopathies.
2. 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.
3. Neuropsychiatric Inventory (NPI-Q) total score =14 or score =4 in any NPI domain
(clinically significant neuropsychiatric symptoms). Apathy score =4 acceptable.
4. 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.
5. Modified Hachinski Scale10 score >4 or evidence of stroke within the past 5
years.
6. 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.
7. 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.
8. History of moderate or more severe traumatic brain injury in the 2 years prior to
signing the consent to participate in the study.
9. History of brain tumor, subdural hematoma, or other clinically significant (in
the judgment of the investigator) space-occupying lesion on MRI.
10. History of seizure disorder.
11. Contraindications for PET scanning or any protocol testing procedure.
3. Systemic related exclusions:
1. 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.
2. 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.
3. 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).
4. Elevated C-reactive protein (>5.0 mg/L) using a high sensitivity test.
5. Fever, signs or symptoms of active illness or infection, or a diagnosed
infectious disease.
6. Immunizations within 4 weeks of the leukapheresis or investigational treatment
(ALZN002 or placebo) administrations.
7. Recent (past 8 weeks) donation of blood or loss of blood (>400 cc).
8. Insulin-dependent diabetes mellitus
4. The following medications are excluded with the noted exceptions:
1. 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
2. Administration of diphenhydramine and/or acetaminophen are prohibited pre- and/or
post-infusion except if, in the opinion of the Investigator on a case-by-case
basis in response to individual subject infusion reaction adverse event(s), these
drugs are judged to be appropriate for immediate treatment of adverse experiences
and/or prophylactically prior to subsequent doses. Also, if adjudicated by the
Sponsor's Expert Panel and Safety Adjudication Committee as appropriate,
conditions of routine use of these drugs can be deployed during the study
3. Treatment with coumarins/indandiones, factor Xa inhibitors, heparins, direct
thrombin inhibitors, and aspirin, except low-dose (81 mg) aspirin for
cardio-protection
4. Benzodiazepines are permitted as a sleep aid only if taken at a stable dose for
at least 60 days prior to Screening and the subject intends to continue to
maintain the same regimen
5. Initiation of medications that could cause or worsen cognitive impairment (ie,
anticholinergic medications, tricyclic antidepressants, antipsychotic medications, and
anticonvulsant medications).
6. Initiation of systemic corticosteroid exposure or any other immunotherapies,
regardless of indication, within 3 weeks prior to or after investigational treatment
(ALZN002 or placebo) administrations, and immunizations within 4 weeks of the
leukapheresis procedure or investigational treatment administrations.
7. Clinical laboratory exclusions:
1. Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >2 x upper
limit of normal (ULN)
2. Total bilirubin >1.5 x ULN unless Gilbert's syndrome
3. Estimated glomerular filtration rate (eGFR) <45 mL/min/1.73 m2 (CKD-EPI 2022
formula)
4. HbA1c >6.5%
5. Hemoglobin <11.0 for males and <9.5 for females, use of red blood cell related
medications/treatments (erythropoietin) within 2 years, history of or current
bone marrow disease or myelodysplastic syndromes.
6. Thyroid stimulating hormone >1.5 x ULN or <0.8 x lower limit of normal (LLN)
8. Electrocardiogram findings of ischemia or infarct, complete bundle branch blocks,
symptomatic arrhythmias or predominantly non-sinus-conducted rhythm, QTcF >460 msec
males or >480 msec females
9. Positive urine drug screen for controlled substances, including tetrahydrocannabinol
or controlled substance(s) for which the subject does not have a valid prescription.
Subjects taking non tetrahydrocannabinol (THC) containing cannabidiol products will
not be excluded unless the urine drug screen is positive for THC.
10. Subjects with a history (within 2 years of screening) of alcohol abuse that, in the
opinion of the Principal Investigator, may impact compliance. Inability to abstain
from alcohol consumption during their stay in the hospital/clinic. A positive blood
alcohol test at screening is also exclusionary.
11. Any other medical, psychiatric, or social condition that, in the opinion of the
investigator, is likely to unfavorably alter the risk-benefit of subject
participation, to interfere with protocol compliance, or to confound safety or
efficacy assessments.
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