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NCT Number: NCT06534723

Phase 3 Clinical Trial of Wujia Yizhi Granules in the Treatment of Mild-to-moderate Alzheimer's Dementia (Syndrome of Deficiency of Spleen and Kidney)

This study is a randomized, double-blind, placebo-controlled phase 3 design aimed at further verifying the safety and efficacy of Wujia Yizhi granules for mild-to-moderate Alzheimer's dementia

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Key information

Age range

50 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Fujian Medical University Affiliated Union Hospital

Fuzhou, Fujian, 350000, China

Location status: Recruiting

About this study

This is a multi-center, randomized, double-blind, placebo-controlled phase 3 clinical trial targeting patients with mild-to-moderate Alzheimer's dementia (TCM differentiated as syndrome of deficiency of spleen and kidney). 570 subjects were recruited and randomly assigned to the experimental and placebo groups at a ratio of 2:1.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female, age range : 50 - 80 years old.
  • Informed consent signed and dated by patient or legal representative.
  • The participants are mild-to-moderate AD patients who meet the diagnostic criteria for AD proposed by the National Institute on Aging and the Alzheimer's Association (NIA-AA) in 2018 and have a disease course of more than 6 months. If participants lack previous pathological evidence or biomarkers of Alzheimer's dementia, they must have evidence of β-amyloid deposition biomarkers during screening (PET with abnormal amyloid deposition or low cerebrospinal fluid Aβ 42 and Aβ 42/Aβ 40 ratio).
  • MMSE score 11 to 26;CDR-GS score 1 to 2 。

Exclusion criteria

  • Participants with non AD induced memory and cognitive impairment, such as diagnosis of other types of dementia, including but not limited to mixed dementia (AD VaD), vascular dementia (VD), Parkinson's disease dementia (PDD), Lewy body dementia (DLB), Huntington's disease related dementia, frontotemporal lobe dementia (FTD), etc; Endocrine system disorders (such as thyroid diseases, parathyroid diseases) and dementia caused by folate, vitamin B12 deficiency, or any other reason; Existence of consciousness disorders, etc.
  • Participants have a history of epileptic seizures.
  • Participants are psychiatric patients, including but not limited to schizophrenia, affective schizophrenic disorder, bipolar disorder, or delirium.
  • HAMD-17 score ≥ 17 points.
  • HAMA score ≥ 14 points.
  • Participants were taking antidepressants, anxieties, and antipsychotic drugs during screening.
  • HIS score ≥ 4 points..

Treatment and study plan

Wujia Yizhi granules

Drug

Drug: Wujia Yizhi granuless

Placebo

Drug

Placebo

Primary outcomes

  1. Change from baseline to endpoint in Alzheimer's dementia Assessment Scale-Cognitive subscore (ADAS-Cog12).

    Time frame: Change from Baseline to Month 12

    The Alzheimer's Disease Assessment Scale - Cognitive Scale (ADAS-Cog12) is used to assess the cognitive function level of AD subjects. The ADAS-Cog12 score range is 0-75 points, and the higher the score on the scale, the more severe the cognitive impairment.

  2. Change from baseline to endpoint in Clinical Dementia Rating-Sum of Boxes (CDR-SB).

    Time frame: Change from Baseline to Month 12

    The Alzheimer's Disease Assessment Scale - Cognitive Scale (CDR-SB) is used to assess the cognitive function level of AD subjects. The CDR-SB score range is 0-3 points, and the higher the score on the scale, the more severe the cognitive impairment.

Secondary outcomes

  1. Change from baseline to endpoint in ADAS-Cog12.

    Time frame: Change from Baseline to month 3, 6, and 9

    The Alzheimer's Disease Assessment Scale - Cognitive Scale (ADAS-Cog12) is used to assess the cognitive function level of AD subjects. The ADAS-Cog12 score range is 0-75 points, and the higher the score on the scale, the more severe the cognitive impairment.

  2. Change from baseline to endpoint in CDR-SB.

    Time frame: Change from Baseline to month 3, 6, and 9

    The Alzheimer's Disease Assessment Scale - Cognitive Scale (CDR-SB) is used to assess the cognitive function level of AD subjects. The CDR-SB score range is 0-3 points, and the higher the score on the scale, the more severe the cognitive impairment.

  3. Change from baseline to endpoint in he Alzheimer's dementia Cooperative Study-Activities of Daily Living (ADCS-ADL) scale.

    Time frame: Change from Baseline to month 3, 6, 9 and 12

    The Alzheimer's Disease Collaborative Study Group - Activities of Daily Living Scale (ADCS-ADL) is used to evaluate the daily living abilities of AD subjects. The score range of ADCS-ADL is from 0 to 78, with higher numbers indicating better daily functioning.

  4. Change from baseline to endpoint in Mini-Mental State Examination (MMSE).

    Time frame: Change from Baseline to month 3, 6, 9 and 12

    The Simple Intelligent State Examination Scale (MMSE) has a total of 19 items, with scores ranging from 0 to 30. In clinical practice, the diagnostic threshold is usually adjusted based on educational level, with university ≤ 26 points, middle school ≤ 24 points, primary school ≤ 23 points, and illiteracy ≤ 22 points, indicating dementia.

  5. Change from baseline to endpoint in Neuropsychiatric Inventory (NPI).

    Time frame: Change from Baseline to month 3, 6, 9 and 12

    The Neuropsychiatric Inventory (NPI) includes a total of 12 items in 10 behavioral domains and 2 autonomic nervous system domains, with a score range of 0-144. The caregiver distress rating is 0-60, where 0 represents the best, and the higher the score, the higher the level of distress.

  6. Change from baseline to endpoint in Traditional Chinese Medicine Syndrome Score

    Time frame: Change from Baseline to month 3, 6, 9 and 12

    TCM syndrome scale was used to evaluate the changes of TCM symptoms and signs before and after treatment.

Study contacts

Contact information is provided by the study sponsor or research team.

Lin song

CONTACT

[email protected]

028-81258178

Sponsors and collaborators

Lead sponsor

Sichuan Jishengtang Pharmaceutical Co., Ltd.

Industry

Registry information

Official study title

A 12-month Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel Group, Phase 3 Clinical Trial of Wujia Yizhi Granules in the Treatment of Mild-to-moderate Alzheimer's Dementia (Syndrome of Deficiency of Spleen and Kidney).

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Aug 2, 2024
Registry last updated
Dec 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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