DL-3-n-butylphthalide Treatment in Patients With Mild to Moderate Alzheimer's Disease Already Receiving Donepezil

Last updated: February 10, 2020
Sponsor: First Affiliated Hospital Xi'an Jiaotong University
Overall Status: Completed

Phase

N/A

Condition

Alzheimer's Disease

Dementia

Memory Loss

Treatment

N/A

Clinical Study ID

NCT02711683
XJTU1AF-CRF-2015-027
  • Ages 50-85
  • All Genders

Study Summary

Alzheimer's disease (AD) is the commonest cause of dementia. There is no effective treatment to cure the disease. Cholinesterase inhibitors, such as donepezil, are widely recommended to patients with mild to moderate AD. But the cognitive function of most of the patients using donepezil gradually aggravate, with Mini-Mental State Examination(MMSE) score falling by 2 points per year on average, and donepezil cannot effectively delay AD progress.

DL-3-n-butylphthalide(NBP) is a synthetic chiral compound containing L- and D-isomers of butylphthalide. It is developed from L-3-n-butylphthalide, which was initially isolated as a pure component from seeds of Apium graveolens in 1978 by researchers of Institute of Medicine of Chinese Academy of Medical Sciences. Studies in the past several decades have demonstrated that NBP is effective in alleviating oxidative damage and mitochondria dysfunction, improving microcirculation. NBP was approved by the State Food and Drug Administration of China (SFDA) as a therapeutic drug for treatment of ischemic stroke in 2005 Not only for ischemic stroke, NBP has been reported to increase the expression of N-methyl-D-aspartate subtype glutamate receptor 2B(NR2B) and synaptophysin in hippocampus of aged rats after chronic cerebral hypoperfusion and increasing brain acetylcholine level, which are important processes involved in learning and memory. It could alleviate the learning and memory deficits induced by cerebral ischemia in rats. A multicentre, randomized, double-blind, placebo-controlled trial conducted by Professor Jia investigated that NBP was effective for improving cognitive and global functioning in patients with subcortical vascular cognitive impairment without dementia and exhibited good safety over the 6-month treatment period. The pathogenesis of AD involved mitochondria dysfunction and microcirculation dysfunction, which are the action targets of NBP. Investigators observed that MMSE score lowering slowly when using NBP treatment in patients with mild to moderate AD already receiving donepezil. But investigators lack of system evaluation and follow-up. Hence, investigators hypothesized that NBP may have therapeutic efficacy for patients with AD and designed the present study.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • literate Chinese, aged 50-85 years, with a consistent caregiver who accompanied thesubjects at least 4 days a week，2 hours a day;

  • complaint and/or informant report of cognitive impairment involving memory and/orother cognitive domains lasting for at least 12 months; and progressing gradually.

  • diagnosis of probable AD according to the National Institute of Neurological andCommunicative Disorders and Stroke-Alzheimer's Disease and Related DisordersAssociation (NINCDS-ADRDA) criteria;

  • a mini-mental state examination (MMSE) score ≥11 and ≤22 (primary school) or ≥11 and ≤26 (junior school or above) ;

  • Hachinski ischemia scale score ≤4;

  • All patients meeting the clinical criteria underwent brain magnetic resonance imaging (MRI) scan including hippocampal assessment at screening. The MRI entry criteria areas follows: the number of cerebral infarcts (≥20 mm in diameter)less than 2, withoutinfarcts in thalamus, hippocampal or entorhinal cortex, the medial temporal lobeatrophy visual rating scale (MTA) score more than 2 degree.

  • absent of neurological sign;

  • having used donepezil more than 3 months and remained relatively stable；

  • sign the informed consent.

Exclusion

Exclusion Criteria:

  • severe white matter lesion(WML)(score ≥3 according to the Fazekas rating scale), thenumber of cerebral infarcts (≥20 mm in diameter)more than 2, with infarcts in theimportant sites, such as thalamus, hippocampal or entorhinal cortex;

  • dementia due to other causes, such as vascular dementia, infection of central nervoussystem，dementia with Lewy body(DLB)，etc

  • suffered from other neurological disease, such as stroke, Parkinson's disease,epilepsy；

  • suffered from mental disorders, such as schizophrenia，bipolar disorder，severedepression, delirium;

  • suffered from unstable or severe disorders of heart, lung, liver, kidney and bloodsystem;

  • Severe impairment of vision and hearing;

  • Using other cholinesterase inhibitors or memantine.

Study Design

Total Participants: 92
Study Start date:
March 01, 2016
Estimated Completion Date:
December 31, 2019

Connect with a study center

  • First Affiliated Hospital of Xi'an Jiaotong University

    Xi'an, Shaanxi 710061
    China

    Site Not Available

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