Efficacy and Safety of Wei Li Bai Capsules in the Treatment of Alzheimer's Disease

Alzheimer Disease Clinical Trial

Official title:

A Randomized, Double-blind, Placebo-controlled, Multi-center II Clinical Trial to Evaluate the Efficacy and Safety of Wei Li Bai Capsules in the Treatment of Mild to Moderate Alzheimer's Disease

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05670912
• Other study ID #: WLB-2022
• Status: Recruiting
• Phase: Phase 2
• Start date: October 1, 2022
• Est. completion date: November 30, 2024

Study information

• Verified date: March 2024
• Source: Capital Medical University
• Contact: Jianping Jia
• Phone: 0086-10
• Email: jjp[@]ccmu.edu.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In clinical trials of preclinical pharmacodynamic studies, Wei Li Bai capsules has been proved to significantly improve the learning and memory ability of Alzheimer's disease model. In this study, the researchers will use a multicenter, randomized, double-blind, placebo-controlled parallel method to recruit Alzheimer's disease patients to confirm the efficacy and safety of Wei Li Bai capsules. Confirmation of drug efficacy will be observed through changes in Alzheimer's disease patients' general cognitive function scores, scores of different cognitive domains, daily living activities, and symptom severities.

Description:

Wei Li Bai Capsule is composed of sodium ferulate tablets, L-rhamnose and chrysin. Sodium ferulate tablet is a domestically marketed drug, L-rhamnose is a marketed food additive, and chrysin is a dietary supplement. All of them have been widely used and their safety has been confirmed. In addition, since these three compounds all show good potential in the treatment of Alzheimer's disease, and play an important role in regulating metabolism, improving blood circulation and anti-inflammatory and antioxidant, this study will explore the synergistic effect of Wei Libai capsule in patients with mild and moderate Alzheimer's disease in 130 subjects.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 130
• Est. completion date: November 30, 2024
• Est. primary completion date: November 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 50 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Age 50 to 80 years old (including 50 and 80 years old), male or female;

2. Meet the diagnostic criteria of "likely ad dementia" of the National Institute on aging Alzheimer's disease association (NIA-AA) (2011);

3. The subjects are primary school graduates / graduates and above, and have the ability to complete the cognitive ability test and other tests specified in the program;

4. Memory loss lasted for at least 6 months and tended to worsen gradually;

5. Subjects with mild or moderate illness: 11 = total score of MMSE = 26;

6. Total score of Clinical Dementia Rating Scale (CDR):

Mild dementia: CDR = 1.0; Moderate dementia: CDR = 2.0;

7. The total score of HIS = 4;

8. The total score of Hamilton Depression Scale (HAMD 17 item version) is = 10;

9. There was no obvious positive sign in nervous system examination;

10. Coronal scanning of head MRI in screening stage: the MTA grade of medial temporal lobe atrophy visual assessment scale is grade 2 or higher, and the signal changes of T2 FLAIR sequence in coronal position of hippocampus. If the subject can provide the head MRI film that meets the requirements within 1 month before screening, it can be used as the basis for enrollment without repeated shooting; If the researcher cannot judge whether the subject's condition has changed, the coronal MRI scan of the head before enrollment can be added;

11. The subjects should have stable and reliable caregivers, who will take care of them at least 3 days a week and at least 4 hours a day. The caregivers will accompany the subjects to participate in the whole process of the study. Caregivers must accompany the subjects to the study visit and assist the investigator in completing the Neuropsychiatric Inventory (NPI), Alzheimer's Disease Collaborative Study-Ability of Daily Living Scale (ADCS-ADL), and Clinician Interview Based Impression of Severity (CIBIC -plus), and other scale scores;

12. Agree to participate and sign the informed consent form by the legal guardian. Due to the subject's limited cognitive ability and other reasons, the subject's signature is allowed to be left blank, and the reason is explained. In addition, the legal guardian shall sign the reason statement, and the legal guardian shall sign the informed consent.

Exclusion Criteria:

1. During screening, MRI examination showed significant focal lesions, fulfilling one of the following conditions: ? There were more than 2 infarcts with diameter > 2 cm at any site; ? MRI examination showed that there were infarcts with arbitrary diameter in key parts (such as thalamus, hippocampus, entorhinal cortex, paraolfactory cortex, angular gyrus, cortex and other subcortical gray matter nuclei); ? Fazekas scale grade of white matter lesions =2; ? There are other imaging evidences that do not support mild and moderate AD.

2. Dementia caused by other reasons: vascular dementia, central nervous system infection, Creutzfeldt Jakob disease, Huntington's disease, Parkinson's disease, Lewy body dementia, traumatic dementia, other physical and chemical factors (such as drug poisoning, alcoholism, carbon monoxide poisoning, etc.), important physical diseases (such as hepatic encephalopathy, pulmonary encephalopathy, etc.), intracranial space occupying lesions (such as subdural hematoma, brain tumor), endocrine disorders (such as thyroid disease, parathyroid disease), and vitamin B12, folic acid deficiency or any other known cause;

3. Have suffered from central nervous system diseases (including stroke, optic neuromyelitis, epilepsy, etc.);

4. Subjects who were diagnosed with psychiatric disorders according to DSM-V criteria, including schizophrenia or other mental diseases, bipolar disorder, severe depression or delirium;

5. Abnormal laboratory indexes: liver function (ALT and AST) exceeded 1.5×ULN, renal function (CR) exceeded 1.5×ULN, and creatine kinase exceeded 2×ULN;

6. Untreated hypertensive and hypotensive subjects at screening, or hypertensive subjects with uncontrolled hypertension after treatment; subjects with good blood pressure control after treatment can be determined by the investigator to be suitable for inclusion in this study;

7. Within 1 month of the screening visit, the subject has new or ongoing unstable or serious heart, lung, liver, kidney and hematopoietic diseases according to the judgment of the researcher, and does not meet the conditions for clinical research;

8. Clinically, people with significant allergic reaction history, especially drug allergy history, or known allergy to this product and its excipients;

9. Dyspepsia, esophageal reflux, gastric bleeding or peptic ulcer disease, frequent heartburn (= once a week) or any surgical operation that may affect drug absorption (such as partial / total gastrectomy, partial / total small bowel resection and cholecystectomy) within 6 months before screening;

10. Alcohol or drug abusers;

11. Human immunodeficiency virus antibody (ant HIV) and Treponema pallidum antibody (ant TP) are positive;

12. Those who are currently using and cannot stop using drugs for Alzheimer's disease;

13. Screening for cholinesterase inhibitors, N-methyl-D-aspartate receptor antagonists (NMDA antagonists), mental retardants, antiparkinsonian drugs and opioid analgesics taken within 1 month before the visit;

14. There are uncorrectable visual and auditory disorders, and the neuropsychological test and scale evaluation cannot be completed;

15. Female subjects with positive pregnancy test or lactation and subjects unable to take effective contraceptive measures or have family planning;

16. Participated in other clinical trials within 3 months before the screening visit;

17. There are other situations that the researcher believes are not suitable to participate in this study.

Related Conditions & MeSH terms

• Alzheimer Disease

Intervention

Drug:
• Wei Li Bai capsules
The distribution ratio between the groups was 1:1, and the stratification factor was the degree of illness CDR score. In the study, the entry of each subject into the active group or placebo group will be determined by the randomized system.
• Placebo Comparator of Wei Li Bai capsules
The distribution ratio between the groups was 1:1, and the stratification factor was the degree of illness CDR score. In the study, the entry of each subject into the active group or placebo group will be determined by the randomized system.

Locations

Country	Name	City	State
China	Beijing Friendship Hospital, Capital Medical University	Beijing
China	Xuanwu Hospital of Capital Medical University	Beijing
China	China-Japan Friendship Hospital	Chaoyang	Beijing

Sponsors (3)

Lead Sponsor	Collaborator
Capital Medical University	Beijing Friendship Hospital, China-Japan Friendship Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Alzheimer's Disease Assessment Scale-Cognitive section(ADAS-cog/11)	Differences between the active group in changes in ADAS cog/11 scores (relative to baseline) at weeks 13 and 26 were compared with the placebo group.; The ADAS-cog assesses cognitive function in seven components: word recall, instruction, structural practice, naming, conceptual practice, orientation, and word recognition. The total score ranges from 0 to 70, with lower scores representing milder disease.	Change from baseline in ADAS-cog scores at Week 26.
Secondary	Alzheimer's Disease Co-operative Study Activities of Daily Living (ADCS-ADL)	Differences between the active group in changes in ADCS-ADL scores (relative to baseline) at weeks 13 and 26 were compared with the placebo group.; The ADCS-ADL scale can reflect the degree of impairment of the subjects' daily life ability, with a total score of 78 points. The higher the score, the better the subjects' living ability.	Change from baseline in ADCS-ADL scores at Week 26.
Secondary	Clinician Interview Based Impression of Severity (CIBIC-plus)	Differences between the active group in changes in CIBIC-plus scores (relative to baseline) at weeks 13 and 26 were compared with the placebo group.; The CIBIC-plus scale is based on interviews with patients and their caregivers by research physicians to ask, record and assess changes in patients' conditions. Outcomes assessed were: Caregiver Meeting-Clinical Impression Change, Subject Meeting-Clinical Impression Change, and Overall Clinical Impression Change.	Change from baseline in CIBIC-plus scores at Week 26.
Secondary	Neuropsychiatric Inventory (NPI)	Differences in changes in 12-item behavioral domain scores (relative to baseline) on the NPI scale at weeks 13 and 26 between the active group compared with placebo group.; The NPI scale is an interview conducted by the research doctor based on the patient's caregiver to ask the patient's mental and emotional changes. The questions included 12 items including delusions, hallucinations, depression, and anxiety, each of which identified the severity, frequency, and psychological stress of the caregiver.	Change from baseline in NPI's 12 behavioral domain scores at week 26.
Secondary	Neuropsychiatric Inventory (NPI)	Differences in changes in caregiver stress scores (relative to baseline) on the NPI scale at weeks 13 and 26 between the active group compared with placebo.	Change from baseline in Caregiver Stress Score on the NPI Scale at Week 26.