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UnknownPhase 2MW150 Stress Kinase Inhibitor in Mild to Moderate Alzheimer's Disease
A Phase 2a Study of MW150 Stress Kinase Inhibitor in Mild to Moderate Alzheimer's Disease
Lead sponsor
Asset
MW150
Listed sites
1
Recruiting sites
-
Enrollment
24
estimated
Study population
Alzheimer’s disease
Key I/E criteria
•Alzheimer's disease•CDR global 0.5-2•MMSE 14-28•Study partner/caregiver required
Primary endpoints
•Drug Safety- Blood tests•Drug Safety- Electrocardiographic•Drug Safety- C-SSRS
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. Signed informed consent from subject (or legally authorized representative, LAR) and study partner.
2. Male or female, age 50 to 90 inclusive.
3. Have a study partner who is able to accompany the subject, has frequent contact with subject.
4. Meet criteria for Alzheimer's Disease by NIAA-AA criteria.
5. Must speak English fluently.
6. Must have education of at least 8 years.
7. Must have adequate hearing and visual abilities.
8. MMSE score of 14 to 28.
9. Clinical Dementia Rating (CDR) Global score of 0.5 to 2.0 inclusive.
10. Absence of suicidal ideation for at least 1 year.
11. Absence of medical conditions that could affect ability to participate in study.
12. MRI within 1 year of screening, not showing clinically significant structural lesions. Subjects without available MRI within 1 year, must have an MRI performed for eligibility.
13. Stable neuropsychiatric medications for at least 2 months prior to screening.
14. If female, must not be of childbearing potential, as defined by being postmenopausal (more than 1 year without periods) or surgically sterile for at least 6 months prior to screening.
15. If male, must agree to use contraception if with a potentially childbearing partner
Exclusion criteria
1. Presence of clinically significant disorders of the central nervous system other than Alzheimer's disease, such as Lewy Body Disease, Parkinson's disease, hydrocephalus, epilepsy, demyelinating disease, brain tumors, or psychiatric disorders (such as schizophrenia, or severe affective disorders).
2. Serious or unstable hematologic, hepatic, renal, pulmonary, cardiac, or other medical disease.
3. Abnormal liver function tests (ALT or AST) or creatine kinase (CK) upon repeat testing.
4. Chronic hepatitis B or C infection, indicated by positive HBSAg, or HCV-Ab with HCV RNA presence.
5. Known history of human immunodeficiency virus (HIV) infection.
6. Known immune disorder that has a history of requiring treatment with immunosuppressive drugs within the past 1 year.
7. Have a drug or alcohol abuse within 12 months prior to screening.
8. Clinically significant laboratory abnormalities at screening.
9. Screening ECG showing repeated QTcF > 480 msec, or other clinically significant ECG abnormalities.
10. Clinically significant structural brain abnormalities, such as hydrocephalus or intra-axial brain tumors.
11. Participation in another investigational study within 30 days or 5 half-lives prior to screening, whichever is greater.
12. Participation in another study that would have cognitive testing during the duration of this study.
13. History of Covid19 or other viral infections within 3 months.
14. Have a clinically significant medical, surgical, laboratory, or behavioral abnormality, which in the judgment of the Investigator makes the subject unsuitable for the study.
Endpoints (13)
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
2 endpointsCognitive change-MMSE
Time frame:84 days treatment
Mini-Mental State Examination (MMSE)
change from baseline, improvement
Cognitive change-ADAScog
Time frame:84 days treatment
ADAS-Cog
change from baseline, improvement
Executive function / language
1 endpointCognitive change-Language
Time frame:84 days treatment
change from baseline, improvement
Function / daily living
1 endpointFunctional performance- ADCS-ADL
Time frame:84 days treatment
ADCS-Activities of Daily Living (ADCS-ADL)
change from baseline, improvement
Behavior / neuropsychiatric
1 endpointBehavioral Scale - NPI-Q
Time frame:84 days treatment
Neuropsychiatric Inventory (NPI)
change from baseline, improvement
Neurodegeneration biomarkers
1 endpointPharmacodynamics - neuronal biomarkers
Time frame:84 days treatment
Neurofilament light (NfL)
descriptive
Safety / tolerability / PK
4 endpointsDrug Safety- Blood tests
Time frame:84 days treatment
event count, event
Drug Safety- Electrocardiographic
Time frame:84 days treatment
event count, event
Drug Safety- C-SSRS
Time frame:84 days treatment
descriptive
Drug Tolerability- Adverse events
Time frame:84 days treatment
event count, event
Other (unclassified)
3 endpointsCognitive change-Executive
Time frame:84 days treatment
change from baseline, improvement
Functional performance-CDR
Time frame:84 days treatment
change from baseline, improvement
Pharmacodynamics - cytokines
Time frame:84 days treatment
descriptive
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.