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Alzheimer's disease
Purpose of Study: To evaluate the efficacy and safety of an investigational drug taken twice daily in adults with mild to moderate Alzheimer's disease compared to placebo.
Inclusion Criteria:
- Age 55+
- Diagnosed with probable Alzheimer's disease
- Must be able to read, understand and speak English
- CT or MRI 12 months prior to screening
- Must have reliable caregiver
Exclusion Criteria:
- Dementias other than Alzheimer's disease
- History or evidence of any other CNS disorder (stroke, hemorrhage, epilepsy, Parkinson's, etc.)
- Hypothyroidism, folic acid deficiency, or vitamin B12 deficiency
- Patients who have to drive during the study
- History of more than 1 myocardial infarction within 5 years before study entry
- Severe hypotension or hypertension requiring treatment unless controlled for at least 3 months
- History of major depressive episodes such as schizophrenia or bipolar affective disorder
- History or presence of gastro-intestinal, hepatic, or renal disease
- History or presence of cancer (excluding carcinoma in situ)
- Treatment with memory/cognitive enhancing drugs within 2 weeks before screening
- Frequent smoker (more than 10 cigarettes/day), frequent consumer of caffeine (more than 6 cups of tea/coffee per day)
- Pregnant or lactating women
- History of drug or alcohol abuse
If you qualify, all study related care is provided at no charge including:
- Study visits and study related procedures/tests
- Laboratory tests
- Study drug
- Possible reimbursement for time and travel
Inclusion/Exclusion Criteria Must Be Met
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