Status:

TERMINATED

A Study to Evaluate the Effects of MK-0249 and an Alzheimer's Disease Medication on Cognitive Function in Adults With Alzheimer's Disease (MK-0249-023)

Lead Sponsor:

Merck Sharp & Dohme LLC

Conditions:

Alzheimer's Disease

Dementia

Eligibility:

All Genders

65+ years

Phase:

PHASE1

Brief Summary

This study will evaluate acute symptomatic improvements in cognitive performance in healthy elderly participants with mild-to-moderate Alzheimer's disease. A four-week pilot study will first evaluate ...

Eligibility Criteria

Inclusion

  • Patient Specific:
  • Female is not of reproductive potential
  • Male who has a female partner(s) of child bearing potential, agrees to use acceptable method of contraception during the study
  • Has at least 10 years of education or work history
  • Has been a nonsmoker or has not used nicotine for at least 6 months
  • Has a diagnosis of mild-to-moderate Alzheimer's Disease
  • Has a reliable caregiver who consents to accompany the patient to all clinic visits, provide information to the study staff, and return for follow-up visits and procedures
  • Healthy Elderly Volunteer Specific:
  • Is in good general health
  • Has no clinically significant abnormality on electrocardiogram (ECG)

Exclusion

  • Participant Specific:
  • Has a history of a neurological disorder other than Alzheimer's disease
  • Is living in a nursing home
  • Has a history of stroke
  • Has a history of psychotic disorder, an active major depressive disorder, or history of schizophrenia
  • Has a history of a sleep disorder
  • Has a history of a cardiovascular disorder
  • Has a history of malignancy
  • Is participating or has participated in a study with an investigational compound, device, or vaccine for Alzheimer's disease
  • Consumes greater than 6 servings of caffeine (coffee, tea or cola etc.) per day
  • Consumes greater than 3 alcoholic beverages per day
  • Has had major surgery, donated or loss blood in past 8 weeks
  • Healthy Elderly Volunteer Specific:
  • Is mentally or legally incapacitated, has significant emotional problems, or has a history of a psychiatric disorder over the last 5-10 years

Key Trial Info

Start Date :

April 6 2009

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 20 2009

Estimated Enrollment :

4 Patients enrolled

Trial Details

Trial ID

NCT00874939

Start Date

April 6 2009

End Date

April 20 2009

Last Update

October 17 2018

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