NCT04730635已完成1 期
A Clinical Study to Evaluate a Cognitive Platform to Support Development of Symptomatic Therapies in Participants at Risk for Alzheimer's Disease
适应症
干预措施
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 44
- 试验地点
- 10
- 主要终点
- Change From Baseline in Averaged Correct Response Rate on the One Card Learning Task to Week 8
研究概览
简要总结
The main purpose of this study is to assess the ability of a repeated high-frequency site-based computerized cognitive assessment to evaluate the potential treatment effects of donepezil (MK-0000) compared with placebo among participants with mild cognitive impairment (MCI) or mild Alzheimer's Disease (AD). The primary study hypothesis is that the average percentage of correct responses on one card learning (OCL) task will be ≥2 percentage points in participants receiving donepezil compared with participants receiving placebo.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Care Provider, Investigator)
盲法说明
Single-blind (placebo run-in) followed by double-blind
入排标准
- 年龄范围
- 55 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Has an Mini Mental State Examination (MMSE) score between 18 and 28 (inclusive) at Screening (Visit 1) and Baseline (Visit 2)
- •Has a diagnosis of mild cognitive impairment (MCI) or mild Alzheimer's Disease (AD)
- •Has an Modified Hachinski Ischemia Scale (MHIS) score of ≤4
- •Must have a reliable and competent study partner/informant who accompanies participant to study visits and participates in assessments
- •Be willing to provide a blood sample for Apolipoprotein E (APOE) genotyping
- •Does not have intellectual disability
- •Be able to speak, read, hear, and understand the language of the study staff and the Informed Consent Form (ICF)
- •Be able and willing to adhere to the study visit schedule
- •Have visual acuity, visual function, hearing, and gross and fine motor skills adequate to support study participation
- •Be capable of performing the Cogstate battery assessments, as demonstrated at the Baseline/Familiarization Visit (Visit 2)
- •A female participant is eligible to participate if she is a woman of nonchildbearing potential (WONCBP)
排除标准
- •Is at imminent risk of self-harm
- •Has evidence of a clinically relevant neurological disorder other than AD at screening, including but not limited to: Parkinson's disease, frontotemporal dementia, Huntington's disease, amyotrophic lateral sclerosis, multiple sclerosis, progressive supranuclear palsy, dementia with Lewy bodies, other types of dementia, neurosyphilis or that led to persistent cognitive deficits, or has a history of seizures or epilepsy within the last 5 years before screening
- •Has a known history of stroke or has a diagnosis of vascular dementia
- •Has history of multiple episodes of head trauma, or head trauma resulting in protracted loss of consciousness, or serious infectious disease affecting the brain, within the prior 3-5 years
- •Has evidence of a clinically relevant or unstable psychiatric disorder, based on Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5), including schizophrenia or other psychotic disorder, bipolar disorder, major depression, or delirium
- •Has a recent or ongoing, uncontrolled, clinically significant medical condition within 2 months of the Screening visit
- •Has a history of cancer
- •Has a relative contraindication to donepezil including sick sinus syndrome, first, second, or third-degree heart block, bradycardia, active gastrointestinal (GI) bleeding, Zollinger-Ellison syndrome, uncontrolled peptic ulcer disease, or uncontrolled asthma
- •Has a history of significant multiple and/or severe allergies or has had an anaphylactic reaction or significant intolerability to prescription or non-prescription drugs or food. Exception: Participants with selected allergies may be enrolled with Sponsor's approval
- •Is positive for Hepatitis B surface antigen (HBsAg), hepatitis C antibodies or human immunodeficiency virus (HIV) [participants with a history of chronic hepatitis C virus with a documented cure and/or a positive serologic test for HCV with a negative HCV viral load may be included]
- •Has clinically significant vitamin B12 or folate deficiency in the 6 months immediately before screening, or vitamin B12 or folate deficiency in addition to increased serum homocysteine and methylmalonic acid levels at screening
- •Has prior AD treatment
- •Has participated in another investigational study within 4 weeks
- •Has a known history of structural changes on screening magnetic resonance imaging (MRI) scan that are clinically important, including signs indicative of vascular dementia, large infarct, lacunes in critical areas, space-occupying lesions, or extensive white matter disease
- •Is unwilling to or not eligible to undergo a MRI scan (if a prior MRI scan is not available)
- •Is pregnant, is attempting to become pregnant, or is nursing children
- •Has a history of alcoholism or drug dependency/abuse within the last 5 years prior to the Screening visit
- •Consumes greater than 3 glasses of alcoholic beverages per day
- •Consumes excessive amounts, defined as greater than 6 servings of coffee, tea, cola, energy drinks, or other caffeinated beverages per day
- •Is a regular user of cannabis, any illicit drugs or has a history of drug abuse within approximately 5 years. A participant who is a recreational user of cannabis or other drugs within the past 2 years can be enrolled as long as recreational use does not meet the definition of drug abuse and participant agrees to refrain from substance use for duration of study participation
- •Participants must have a negative urine drug screen (UDS) prior to randomization
- •Had major surgery within 3 months prior to the Screening visit that would interfere in the participant's ability to fully participate in the study
- •Has undergone neuropsychological testing (including the MMSE) or cognitive remediation in the past 4 weeks
- •Is or has an immediate family member who is investigational site or Sponsor staff directly involved with this study
研究组 & 干预措施
Donepezil
Experimental
Participants receive donepezil in doses up to 10 mg once daily (QD), orally in a scheduled titration for Days 1-56. The total treatment duration is 56 days.
干预措施: Donepezil (Drug)
Placebo
Placebo Comparator
Participants receive placebo QD, orally for Days 1-56. The total treatment duration is 56 Days.
干预措施: Placebo (Drug)
结局指标
主要结局
Change From Baseline in Averaged Correct Response Rate on the One Card Learning Task to Week 8
时间窗: Baseline, Up to Week 8
One Card Learning (OCL) uses a pattern separation paradigm to assess visual memory. The change from baseline of correct responses on the OCL task up to Week 8 is compared in participants receiving donepezil with participants receiving placebo. Change from baseline was the averaged correct response rate at Week 8 minus the correct response rate at baseline.
次要结局
- Change From Baseline in Standard Deviation for Averaged Correct Response Rate on the OCL Task (Arcsine Square Root Transformed) to Week 8(Baseline, Up to Week 8)
- Change From Baseline in Averaged Correct Response Rate on the OCL Task to Week 8 in Participants Receiving Donepezil(Baseline, Up to Week 8)
研究者
研究点 (10)
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