Skip to main content
Delfa

← Trials/Trial dossier/NCT04994483

RETHINK-ALZ

CompletedPhase 3Results posted

Simufilam 100 mg for Mild-to-Moderate Alzheimer's Disease

A Phase 3, Randomized, Double-blind, Placebo-controlled, Parallel-group, 52-week Study Evaluating the Safety and Efficacy of Simufilam 100 mg Tablets in Subjects With Mild-to-Moderate Alzheimer's Disease

Asset

Simufilam

Listed sites

88

Recruiting sites

-

Enrollment

804

actual

Study population

Alzheimer’s disease

Key I/E criterion

MMSE 16-27

Primary endpoints

ADAS-CogADCS-Activities of Daily Living (ADCS-ADL)

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

NCT IDNCT04994483
Org study IDPTI-125-07

Timeline

Milestones

Study first posted2021-08-06actual
Study start2021-11-03actual
Primary completion2024-10-02actual
Study completion2024-10-02actual
Last update posted2025-05-25actual
Results first posted2025-05-25actual

Assets

Drug assets

Study populations

Who this study enrolls

Alzheimer’s disease

Eligibility

Who can enroll

Minimum age50 Years
Maximum age87 Years
SexAll
Healthy volunteersNot accepted

Inclusion criteria

Key Inclusion Criteria:

1. Meets National Institute on Aging and Alzheimer's Association Research Framework criteria for individuals in clinical Stage 4 or 5 of the Alzheimer's continuum.

2. Evidence for AD pathophysiology, confirmed either prior to or during screening.

3. MMSE score ≥ 16 and ≤ 27 at screening.

4. Clinical Dementia Rating - Global Score must be 0.5, 1 or 2.

5. If receiving background AD medications, the dosing regimen must be stable for at least 12 weeks prior to randomization. Chronic medications for conditions other than AD (such as depression) must be prescribed at a stable dose for at least 4 weeks prior to screening.

6. The subject has not been a cigarette smoker or chewed tobacco for at least 3 years.

7. Availability of a study partner.

8. Individuals who have participated in a clinical study with an investigational drug targeting the underlying AD process may be permitted to participate in this study.

9. Completed a COVID-19 vaccine primary series ("fully vaccinated") at least 2 weeks prior to randomization or had an unambiguous COVID-19 infection diagnosed more than 3 months before the start of the Screening Period

Exclusion criteria

1. A neurologic condition other than AD that significantly contributes to the subject's dementia.

2. Any current primary psychiatric diagnosis other than AD if it is likely to confound cognitive assessment or ability to comply with study procedures.

3. Geriatric Depression Scale (15-item) score > 8. (Note - a subject with a score > 8 may continue in screening if, in the judgment of the Investigator, the elevated score is not attributed to a major depressive episode).

4. Suicidal ideation during the past 3 months or suicidal behavior during the past 12 months.

5. Alcohol or substance use disorder within 2 years of screening.

6. MRI presence of cerebral vascular or other significant pathology.

7. History of transient ischemic attack or stroke within 12 months of screening

8. Seizure within 12 months of screening.

9. Severe head trauma or head trauma considered likely to be contributing to the subject's cognitive impairment.

10. Sleep apnea that is considered likely to be contributing to the subject's cognitive impairment.

11. Insufficiently controlled diabetes mellitus or hypertension.

12. Body mass index < 18.5 or > 37.5.

13. History or diagnosis of clinically significant cardiac disease

14. Currently or previously prescribed/administered aducanumab, lecanemab, or any anti-amyloid monoclonal antibody, more than 2 doses.

Endpoints (18)

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
Memory
2
Function / daily living
2
Behavior / neuropsychiatric
2
Tau biomarkers
2
Fluid / digital biomarkers
2
Caregiver / quality of life
2
Other (unclassified)
2

Global cognition

4 endpoints
Secondary/protocol endpoint

Change From Baseline in the Mini-Mental State Exam (MMSE)

Time frame:Baseline (Study Day 1) to Week 52

Mini-Mental State Examination (MMSE)

change from baseline, improvement

Secondary/protocol endpoint

Change From Baseline in the Clinical Dementia Rating Sum of Boxes (CDR-SB)

Time frame:Baseline (Study Day 1) to Week 52

Clinical Dementia Rating-Sum of Boxes (CDR-SB)

change from baseline, improvement

Secondary/registry result

Change From Baseline in the Mini-Mental State Exam (MMSE)

Time frame:Baseline (Study Day 1) to Week 52

Mini-Mental State Examination (MMSE)

change from baseline, improvement

Posted result

GroupValue (least_squares_mean), score on a scaleStandard error
Simufilam 100 mgn=309 Participants-1.950.223
Placebon=324 Participants-2.140.221
Secondary/registry result

Change From Baseline in the Clinical Dementia Rating Sum of Boxes (CDR-SB)

Time frame:Baseline (Study Day 1) to Week 52

Clinical Dementia Rating-Sum of Boxes (CDR-SB)

change from baseline, improvement

Posted result

GroupValue (least_squares_mean), score on a scaleStandard error
Simufilam 100 mgn=334 Participants1.040.138
Placebon=339 Participants0.850.136

Memory

2 endpoints
Primary/protocol endpoint

Change From Baseline in the 12-item Alzheimer's Disease Assessment Scale - Cognitive Subscale (ADAS-Cog12)

Time frame:Baseline (Study Day 1) to Week 52

ADAS-Cog

change from baseline, improvement

Primary/registry result

Change From Baseline in the 12-item Alzheimer's Disease Assessment Scale - Cognitive Subscale (ADAS-Cog12)

Time frame:Baseline (Study Day 1) to Week 52

ADAS-Cog

change from baseline, improvement

Posted result

GroupValue (least_squares_mean), score on a scaleStandard error
Simufilam 100 mgn=306 Participants2.790.363
Placebon=320 Participants3.190.359
Mean Difference (Final Values)-0.3995% CI-1.37 - 0.59p0.4308Mixed Models Analysis

Function / daily living

2 endpoints
Primary/protocol endpoint

Change From Baseline in the Alzheimer's Disease Cooperative Study - Activities of Daily Living (ADCS-ADL)

Time frame:Baseline (Study Day 1) to Week 52

ADCS-Activities of Daily Living (ADCS-ADL)

change from baseline, improvement

Primary/registry result

Change From Baseline in the Alzheimer's Disease Cooperative Study - Activities of Daily Living (ADCS-ADL)

Time frame:Baseline (Study Day 1) to Week 52

ADCS-Activities of Daily Living (ADCS-ADL)

change from baseline, improvement

Posted result

GroupValue (least_squares_mean), score on a scaleStandard error
Simufilam 100 mgn=306 Participants-3.260.442
Placebon=320 Participants-3.760.438
Mean Difference (Final Values)0.5195% CI-0.68 - 1.70p0.4034Mixed Models Analysis

Behavior / neuropsychiatric

2 endpoints
Secondary/protocol endpoint

Change From Baseline in the Neuropsychiatric Inventory (NPI)

Time frame:Baseline (Study Day 1) to Week 52

Neuropsychiatric Inventory (NPI)

change from baseline, improvement

Secondary/registry result

Change From Baseline in the Neuropsychiatric Inventory (NPI)

Time frame:Baseline (Study Day 1) to Week 52

Neuropsychiatric Inventory (NPI)

change from baseline, improvement

Posted result

GroupValue (least_squares_mean), score on a scaleStandard error
Simufilam 100 mgn=301 Participants0.540.588
Placebon=316 Participants0.900.579

Tau biomarkers

2 endpoints
Other/protocol endpoint

Changes From Baseline in Plasma Biomarkers

Time frame:Baseline (Study Day 1) to Week 52

Phosphorylated tau 217 (p-tau217)

change from baseline, improvement

Other_pre_specified/registry result

Changes From Baseline in Plasma Biomarkers

Time frame:Baseline (Study Day 1) to Week 52

Phosphorylated tau 217 (p-tau217)

change from baseline, improvement

Posted result

GroupValue (mean), pg/mLStandard deviation
Simufilam 100 mgP-tau217n=45 Participants1.06.56
GFAPn=45 Participants2.057.39
NfLn=45 Participants69.3373.43
Total taun=45 Participants5.535.62
PlaceboP-tau217n=45 Participants-0.49.77
GFAPn=46 Participants40.2255.14
NfLn=46 Participants17.596.73
Total taun=46 Participants-2.241.98

Fluid / digital biomarkers

2 endpoints
Other/protocol endpoint

Changes From Baseline in the Plasma SavaDx Biomarker

Time frame:Baseline (Study Day 1) to Week 52

change from baseline, improvement

Other_pre_specified/registry result

Changes From Baseline in the Plasma SavaDx Biomarker

Time frame:Baseline (Study Day 1) to Week 52

change from baseline, improvement

Caregiver / quality of life

2 endpoints
Secondary/protocol endpoint

Change From Baseline in the Zarit Burden Interview (ZBI)

Time frame:Baseline (Study Day 1) to Week 52

change from baseline, improvement

Secondary/registry result

Change From Baseline in the Zarit Burden Interview (ZBI)

Time frame:Baseline (Study Day 1) to Week 52

change from baseline, improvement

Posted result

GroupValue (least_squares_mean), score on a scaleStandard error
Simufilam 100 mgn=308 Participants2.520.556
Placebon=321 Participants2.300.551

Other (unclassified)

2 endpoints
Secondary/protocol endpoint/low confidence

Change From Baseline in the Integrated Alzheimer's Disease Rating Scale (iADRS)

Time frame:Baseline (Study Day 1) to Week 52

change from baseline, improvement

Secondary/registry result/low confidence

Change From Baseline in the Integrated Alzheimer's Disease Rating Scale (iADRS)

Time frame:Baseline (Study Day 1) to Week 52

change from baseline, improvement

Posted result

GroupValue (least_squares_mean), score on a scaleStandard error
Simufilam 100 mgn=302 Participants-5.530.605
Placebon=317 Participants-6.490.598

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 tableClinicalTrials.gov results section

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.