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UnknownPhase 3

Octohydroaminoacridine Succinate Tablet for Mild-to-Moderate Alzheimer's Disease

Phase III Trial of Octohydroaminoacridine Succinate Tablet for Mild-to-Moderate Alzheimer's Disease: a 26 Weeks, Randomized, Double-blind, Double-dummy, Placebo- and Positive- Parallel Controlled and Extended Single Arm to 54 Weeks Multicentre Study

Assets

Donepezil / Octohydroaminoacridine succinate

Listed sites

1

Recruiting sites

1

Enrollment

600

estimated

Study population

Alzheimer’s disease

Key I/E criteria

mild-to-moderate ADMMSE 11-26

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

NCT IDNCT03283059
Org study IDOHAAS-III

Timeline

Milestones

Study start2017-08-16actual
Study first posted2017-09-14actual
Last update posted2019-10-22actual
Primary completion2020-09-16estimated
Study completion2021-02-16estimated

Assets

Drug assets

Study populations

Who this study enrolls

Alzheimer’s disease

Eligibility

Who can enroll

Minimum age50 Years
Maximum age85 Years
SexAll
Healthy volunteersNot accepted

Inclusion criteria

1. Age 50-85 years (including 50 and 85 years old), male or female;

2. Diagnose probable AD in accordance with the National Institute Aging and Alzheimer's Association (NIA-AA) (2011);

3. Mild-to-moderate AD patients, MMSE 11-26 (including 11 and 26, primary school education subjects from 11 to 22);

4. Hachinski Incheinic Score (HIS) less than 4 points;

5. Hamilton depression scale /17 Version (HAMD) score less than 10 points;

6. Memory decline at least 12 months, and the decline is progressive;

7. Brain MRI examination was done within 6 months before screening;

8. Neurological examination had no obvious signs (except due to AD disease or peripheral injury);

9. Females were postmenopausal (menopause beyond 24 weeks), or accepted the surgical sterilization, or women of childbearing age agreed to take effective contraceptive measures during the study. Women of childbearing age or menopausal time shorter than 24 weeks must do the urine pregnancy test and results to be negative during the screening period;

10. Subjects should have stable and reliable caregivers, or have frequent contact with caregivers (at least 4 days per week, at least 2 hours per day), caregivers will help patients to participate in the study. Caregivers must accompany the subjects in the study visit to provide valuable information for the NPI, ADCS-ADL and CIBIC-plus scales assessments;

11. Subjects have at least primary school education level, and have the ability to complete the determination of cognitive ability assessments and other tests;

12. The participants and legal guardian must sign informed consent

Exclusion criteria

1. Brain MRI examination showed significant focal lesions, moderate-to-severe white matter lesions, and key parts lacunar infarction such as the thalamus, hippocampus, entorhinal cortex, cortical and subcortical gray matter nuclei;

2. Other type of dementia except AD;

3. Suffered from nervous system diseases (including stroke, optic myelopathy, Parkinson's disease, epilepsy, etc);

4. Psychotic patients, according to the DSM-5 criteria, include schizophrenia or other psychiatry disorders, bipolar disorder, major depression disorder, or delirium;

5. Abnormal laboratory test results: HBsAg and HBeAg and/or HbcAb positive and active stage of hepatitis B, liver function (ALT, AST) more than 1.2 times of the upper limit of the normal range, Cr exceeds the upper limit of normal, white blood cell count less than 4 x 109/L or platelet less than 100 x 109/L, hemoglobin less than 100g/L, blood glucose concentration of diabetic subjects (random) is more than 13.9mmol/L;

6. Systolic pressure was more than 160mmHg or less than 90mmHg, diastolic blood pressure was more than 100mmHg or less than 60mmHg;

7. With unstable or serious heart, lung, liver, kidney and hematopoietic system diseases (including unstable angina, myocardial infarction, uncontrolled asthma, gastric cancer, et al), or resting heart rate after 10 minutes of rest was less than 60 BPM, or QTc (QTc B (Bazett's correction value) or QTc F (Fridericia's correction value)) was equal or greater than 450msec, or with bundle branch block, the QTc B or QTc F was equal or greater than 480msec, or the researchers estimate there were abnormal EKG results which cannot be randomized to the study;

8. There was uncorrected of visual and auditory disturbances, and neuropsychological tests and scale assessments cannot be completed by the subject;

9. Subject was currently using Alzheimer's disease drugs and cannot be terminate the treatment;

10. Subjects that cannot take the test drug according to the prescription should be excluded;

11. Alcohol abuse or drug abuse;

12. Pregnant or lactating women;

13. Participated in other clinical pharmacological tests within 30 days before screening visit;

14. The researchers believe that the subject was impossible to complete the study;

15. Participants were employees of the study and immediate family members, employees of CRO company or sponsor and their immediate family members.

Endpoints (4)

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
1
Function / daily living
1
Behavior / neuropsychiatric
1
Other clinical outcomes
1

Global cognition

1 endpoint
Primary/protocol endpoint

Alzheimer's Disease Assessment Scale-Cognitive section (ADAS-Cog)

Time frame:26 weeks double-blind study and 28 weeks extention study

ADAS-Cog

descriptive

Function / daily living

1 endpoint
Secondary/protocol endpoint

Activities of Daily Living (ADL)

Time frame:26 weeks double-blind study and 28 weeks extention study

descriptive

Behavior / neuropsychiatric

1 endpoint
Secondary/protocol endpoint

Neuropsychiatric Inventory (NPI)

Time frame:26 weeks double-blind study and 28 weeks extention study

Neuropsychiatric Inventory (NPI)

descriptive

Other clinical outcomes

1 endpoint
Secondary/protocol endpoint

Clinician's Interview Based Impression of Change - plus (CIBIC+)

Time frame:26 weeks double-blind study and 28 weeks extention study

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.