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UnknownPhase 2

MW150 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

Asset

MW150

Listed sites

1

Recruiting sites

-

Enrollment

24

estimated

Study population

Alzheimer’s disease

Key I/E criteria

Alzheimer's diseaseCDR global 0.5-2MMSE 14-28Study partner/caregiver required

Primary endpoints

Drug Safety- Blood testsDrug Safety- ElectrocardiographicDrug 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

Org study IDMW150-AD-201
NCT IDNCT05194163
NihR44AG071388

Timeline

Milestones

Study first posted2022-01-18actual
Last update posted2022-03-29actual
Study start2022-05-01estimated
Primary completion2024-08-31estimated
Study completion2024-11-30estimated

Assets

Drug assets

Study populations

Who this study enrolls

Alzheimer’s disease

Eligibility

Who can enroll

Minimum age50 Years
Maximum age90 Years
SexAll
Healthy volunteersNot accepted

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

Safety / tolerability / PK
4
Other (unclassified)
3
Global cognition
2
Executive function / language
1
Function / daily living
1
Behavior / neuropsychiatric
1
Neurodegeneration biomarkers
1

Global cognition

2 endpoints
Secondary/protocol endpoint

Cognitive change-MMSE

Time frame:84 days treatment

Mini-Mental State Examination (MMSE)

change from baseline, improvement

Secondary/protocol endpoint

Cognitive change-ADAScog

Time frame:84 days treatment

ADAS-Cog

change from baseline, improvement

Executive function / language

1 endpoint
Secondary/protocol endpoint

Cognitive change-Language

Time frame:84 days treatment

change from baseline, improvement

Function / daily living

1 endpoint
Secondary/protocol endpoint

Functional performance- ADCS-ADL

Time frame:84 days treatment

ADCS-Activities of Daily Living (ADCS-ADL)

change from baseline, improvement

Behavior / neuropsychiatric

1 endpoint
Secondary/protocol endpoint

Behavioral Scale - NPI-Q

Time frame:84 days treatment

Neuropsychiatric Inventory (NPI)

change from baseline, improvement

Neurodegeneration biomarkers

1 endpoint
Secondary/protocol endpoint

Pharmacodynamics - neuronal biomarkers

Time frame:84 days treatment

Neurofilament light (NfL)

descriptive

Safety / tolerability / PK

4 endpoints
Primary/protocol endpoint

Drug Safety- Blood tests

Time frame:84 days treatment

event count, event

Primary/protocol endpoint

Drug Safety- Electrocardiographic

Time frame:84 days treatment

event count, event

Primary/protocol endpoint

Drug Safety- C-SSRS

Time frame:84 days treatment

descriptive

Primary/protocol endpoint

Drug Tolerability- Adverse events

Time frame:84 days treatment

event count, event

Other (unclassified)

3 endpoints
Secondary/protocol endpoint/low confidence

Cognitive change-Executive

Time frame:84 days treatment

change from baseline, improvement

Secondary/protocol endpoint/low confidence

Functional performance-CDR

Time frame:84 days treatment

change from baseline, improvement

Secondary/protocol endpoint/low confidence

Pharmacodynamics - cytokines

Time frame:84 days treatment

descriptive

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.