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Sirtuin-NAD Activator in Alzheimer's Disease
A Proof of Concept Trial of a Sirtuin-NAD Activator in Alzheimer's Disease
Lead sponsor
Asset
MIB-626
Listed sites
1
Recruiting sites
-
Enrollment
22
actual
Study population
Alzheimer’s disease
Key I/E criteria
•Amyloid biomarker required (CSF)•CDR global 0.5•MMSE 18-26•Study partner/caregiver required•Current anticoagulant use excluded
Primary endpoint
•CSF concentrations of MIB-626
Footprint
Where this trial recruits
Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.
Identifiers
Registered as
Timeline
Milestones
Assets
Drug assets
Study populations
Who this study enrolls
Eligibility
Who can enroll
Inclusion criteria
1. A man or a woman between the ages of 55 and 85 years (inclusive)
2. Meets National Institute on Aging-Alzheimer's Association (NIA-AA) clinical diagnostic criteria for AD dementia
3. Has evidence of AD pathological process by a positive amyloid assessment with cerebrospinal fluid (CSF) Aβ42
4. Has a Clinical Dementia Rating (CDR) global score of 0.5 or 1
5. Has a Mini-Mental State Exam (MMSE) Score of 18 to 26 (inclusive)
6. Has a 15-item Geriatric Depression Scale (GDS) score of < 6
7. Impaired memory performance below education adjusted cut-off score on the Logical Memory II subscale delayed paragraph recall (LM-IIa) of the Wechsler Memory Scale-Revised (WMS-R) (≥16 years: ≤8; 8-15 years: ≤4; 0-7 years: ≤2)
8. May take Food and Drug Administration (FDA) approved medications for the treatment of AD dementia (cholinesterase inhibitors and/or memantine), but if taking such medications, they must be stable for at least 8 weeks before screening
9. Has adequate visual and auditory acuity to participate in neuropsychological testing and other study assessments
10. Has the availability of an informant (study partner) who has regular contact with the participant and knows him/her well
11. Is willing and able to participate in all assessments in English
12. Is capable of providing written informed consent
Exclusion criteria
Subjects may not be enrolled if:
1. Neurologic diseases: Any significant neurologic disease other than AD that can lead to cognitive impairment, such as Parkinson's disease, vascular dementia, dementia with Lewy bodies, frontotemporal dementia, Huntington's disease, normal pressure hydrocephalus, corticobasal syndrome, brain tumor, seizure disorder, subdural hematoma (within the last 1 year), multiple sclerosis, or history of significant head trauma (e.g. loss of consciousness for 30 minutes or more) followed by persistent neurologic deficits or known structural brain abnormalities.
2. Neuroimaging: Baseline or prior magnetic resonance imaging (MRI) scans with evidence of cortical stroke or hemorrhage, strategically located lacunar stroke (ex: left thalamus), or severe small vessel ischemic disease.
3. History of alcohol or substance use disorder or dependence (DSM V criteria) within the last 2 years.
4. Psychiatric disorder: Major depressive disorder (within the last 1 year), bipolar disorder, schizophrenia (DSM V criteria), or current major psychotic symptoms or behavioral problems that could interfere with study procedures.
5. Any significant systemic illness or unstable medical condition, which could obfuscate cognitive aging or neurodegenerative trajectories or affect valid cognitive and self-report measurements.
6. Excluded medications: Niacin or dietary supplements containing nicotinamide mononucleotide (NMN) or nicotinamide riboside (NR); antipsychotic medications, antidepressant medications with anticholinergic side effects. Washout from psychoactive medications for at least 8 weeks before screening.
7. Current use of anticoagulants; significant back or spine disease that would make a lumbar puncture difficult or unsafe as determined by a clinician.
8. Other laboratory abnormalities: Has AST or ALT > 3 times the upper limit of normal; serum creatinine > 2.0 mg/d; HbA1C > 8.5%
9. Participation in an investigational trial to evaluate pharmaceuticals or biologics within the past 3 months or 5 half-lives, whichever is shorter
10. Other medical conditions which, in the opinion of the investigator, would jeopardize safety or impact the validity of the study results.
Endpoints (10)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Coverage by outcome category
Global cognition
1 endpointChange in cognition
Time frame:90
ADAS-Cog
change from baseline, improvement
Function / daily living
1 endpointChange in instrumental activities of daily living (IADL)
Time frame:90
change from baseline, improvement
Behavior / neuropsychiatric
1 endpointChange in neuropsychiatric symptoms
Time frame:90
Neuropsychiatric Inventory (NPI)
change from baseline, improvement
Amyloid biomarkers
2 endpointschange in CSF concentrations of biomarkers of amyloid deposition (Aβ-42, Aβ-40), neuronal/axonal degeneration (t-tau, p-tau, NFL), synaptic function (neurogranin) and neuroinflammation (YKL40, GFAP)
Time frame:90 days
Neurofilament light (NfL)
change from baseline, improvement
Change in circulating biomarkers of amyloid deposition (Aβ-42, Aβ-40), neuronal/axonal degeneration (t-tau, p-tau, NFL), synaptic function (neurogranin), and neuroinflammation (YKL40, GFAP)
Time frame:90
Neurofilament light (NfL)
change from baseline, improvement
Neuroimaging
1 endpointchange in the abundance of NAD in the brain using ultra-high field 7T magnetic resonance spectroscopy
Time frame:90 days
change from baseline, improvement
Fluid / digital biomarkers
2 endpointschange in CSF concentrations of MIB-626
Time frame:90 days
change from baseline, improvement
change in CSF concentrations of MIB-626 metabolites, nicotinamide (NAM), NR, 2-PY, and MeNAM
Time frame:90 days
change from baseline, improvement
Other (unclassified)
2 endpointschange in NAD concentrations in peripheral blood mononuclear cells
Time frame:90 days
change from baseline, improvement
change in the concentration of biomarkers of aging recommended (HbA1C, IGF1, T3, IL6, TNF-alpha, and urinary F2-isoprostane)
Time frame:90 days
change from baseline, improvement
Publications (1)
Bibliography
Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.
Registry references + supporting bibliography
- PMID42063312via DERIVED
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 21, 2026 snapshot.