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Masitinib in Patients With Mild Alzheimer's Disease
A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Phase 3 Clinical Trial to Evaluate the Safety and Efficacy of Masitinib as add-on Therapy in Patients With Mild Alzheimer's Disease, Treated With Standard of Care
Lead sponsor
Asset
Masitinib
Listed sites
9
Recruiting sites
-
Enrollment
600
estimated
Study population
Alzheimer’s disease
Key I/E criteria
•Alzheimer's disease•Amyloid biomarker required (PET)•Tau biomarker required (CSF)•MMSE 21-25•Study partner/caregiver required
Primary endpoint
•ADAS-Cog
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
Main inclusion criteria include:
1. Patient with clinical diagnosis of Alzheimer's disease based on criteria defined by IWG (International Working Group on Alzheimer's disease) at screening visit.
2. Patients with ADCS-ADL score at screening visit and baseline visit < 73
3. Patient with MMSE ≥ 21 and ≤ 25 at screening visit and baseline visit.
4. Patient with Alzheimer's Disease biomarker profile at screening visit:
5. If patients are treated with cholinesterase inhibitors (donepezil, rivastigmine or galantamine), and/or memantine. They should have been at stable dose for a minimum of 6 months at baseline visit, with no changes foreseen in therapy throughout the trial.
6. If receiving a supplement for cognition (eg, gingko biloba, omega-3 polyunsaturated fatty acid, vitamin E, curcumin, souvenaid) patients must have been taking it at stable dose for at least 4 months prior to screening visit.
7. Patients with a caregiver who, at screening and baseline visits, agrees to accompany the participant to all trial visits, supervise compliance with procedures, provide detailed information, has sufficient contact (≥1 hour/day for ≥3 days/week or as deemed sufficient by the Investigator), can read, understand, and speak the designated language, and is cognitively capable of fulfilling trial requirements
Exclusion criteria
include:
Related to disease
1. Patients with any other cause of dementia shown by MRI findings and neurological examination
2. Systemic conditions known to cause dementia, e.g., hypothyroidism, untreated vitamin B12 or folic acid deficiency, niacin deficiency, neurosyphilis, HIV infection at screening visit.
3. Patients with substance-induced dementia, Alzheimer's disease with delirium, severe delusions (e.g., NPI delusion score ≥ 4), psychosis or antipsychotic use, or a history of significant psychiatric disorders at the screening visit.
4. Patients with a significant unexplained improvement or decline in overall status on ADAS-Cog and ADCS-ADL at screening and baseline compared to previous assessments, and those whose scores are not in line with their medical history.
Endpoints (11)
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
4 endpointsAbsolute change from baseline in Mini-Mental State Examination (MMSE) at week 24
Time frame:24 weeks
Mini-Mental State Examination (MMSE)
change from baseline, improvement
Clinical Responder rate
Time frame:24 weeks
ADAS-Cog
threshold achievement, improvement
Absolute change from baseline in CDR
Time frame:24 weeks
change from baseline, improvement
Time to severe dementia (MMSE<10)
Time frame:24 weeks
Mini-Mental State Examination (MMSE)
time to event, event
Function / daily living
2 endpointsAbsolute change from baseline in ADCS-ADL score
Time frame:48 weeks
ADCS-Activities of Daily Living (ADCS-ADL)
change from baseline, improvement
Absolute change from baseline in ADCS-ADL score at week 24
Time frame:24 weeks
ADCS-Activities of Daily Living (ADCS-ADL)
change from baseline, improvement
Behavior / neuropsychiatric
1 endpointAbsolute change from baseline in Neuropsychiatric Inventory (NPI) at week 24
Time frame:24 weeks
Neuropsychiatric Inventory (NPI)
change from baseline, improvement
Caregiver / quality of life
1 endpointCIBIC-plus
Time frame:24 weeks
descriptive
Other (unclassified)
3 endpointsAbsolute change from baseline in iADRS score at week 24
Time frame:24 weeks
ADAS-Cog
change from baseline, improvement
Absolute change from baseline in ADAS-Cog11 score at week 24
Time frame:24 weeks
ADAS-Cog
change from baseline, improvement
Absolute change from baseline in ADAS-Cog11 score at week 48
Time frame:48 weeks
ADAS-Cog
change from baseline, improvement
Publications (3)
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
- PMID21504563via BACKGROUND
- PMID36849969via BACKGROUND
- PMID32623401via BACKGROUND
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.