Skip to main content
Delfa

← Trials/Trial dossier/NCT05040321

CompletedPhase 1 / PHASE2

Sirtuin-NAD Activator in Alzheimer's Disease

A Proof of Concept Trial of a Sirtuin-NAD Activator in Alzheimer's Disease

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 0.5MMSE 18-26Study partner/caregiver requiredCurrent 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

Org study ID2021P001366
Secondary IDMIB-ADMetro International Biotech, LLC
NCT IDNCT05040321

Timeline

Milestones

Study first posted2021-09-10actual
Study start2021-12-01actual
Primary completion2025-12-15actual
Study completion2026-04-30actual
Last update posted2026-07-01actual

Assets

Drug assets

Study populations

Who this study enrolls

Alzheimer’s disease

Eligibility

Who can enroll

Minimum age55 Years
Maximum age85 Years
SexAll
Healthy volunteersNot accepted

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

Amyloid biomarkers
2
Fluid / digital biomarkers
2
Other (unclassified)
2
Global cognition
1
Function / daily living
1
Behavior / neuropsychiatric
1
Neuroimaging
1

Global cognition

1 endpoint
Other/protocol endpoint

Change in cognition

Time frame:90

ADAS-Cog

change from baseline, improvement

Function / daily living

1 endpoint
Other/protocol endpoint

Change in instrumental activities of daily living (IADL)

Time frame:90

change from baseline, improvement

Behavior / neuropsychiatric

1 endpoint
Other/protocol endpoint

Change in neuropsychiatric symptoms

Time frame:90

Neuropsychiatric Inventory (NPI)

change from baseline, improvement

Amyloid biomarkers

2 endpoints
Other/protocol endpoint

change 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

Other/protocol endpoint

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 endpoint
Secondary/protocol endpoint

change 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 endpoints
Primary/protocol endpoint

change in CSF concentrations of MIB-626

Time frame:90 days

change from baseline, improvement

Secondary/protocol endpoint

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 endpoints
Secondary/protocol endpoint/low confidence

change in NAD concentrations in peripheral blood mononuclear cells

Time frame:90 days

change from baseline, improvement

Secondary/protocol endpoint/low confidence

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.

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 21, 2026
Endpoint classificationDelfa ADRD endpoint taxonomy
Results tableno registry results posted yet

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.