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The primary purpose of the study is to assess whether SAM-531, an investigational drug, is safe and well tolerated, compared with placebo (a medically inactive substance), in subjects with mild to moderate Alzheimer's disease.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental |
| |
| 2 | Placebo Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| SAM-531 | Drug |
| ||
| placebo |
| Measure | Description | Time Frame |
|---|---|---|
| Routine safety and tolerability will be evaluated. | 28 days |
| Measure | Description | Time Frame |
|---|---|---|
| This study will also investigate the pharmacokinetics(PK, how the drug is metabolized) and pharmacodynamics (PD, how the drug affects bodily and mental function) of SAM-531 compared to placebo. | 28 days |
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Inclusion Criteria
Exclusion Criteria
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| Name | Affiliation | Role |
|---|---|---|
| Medical Monitor | Wyeth is now a wholly owned subsidiary of Pfizer | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Delray Beach | Florida | 33445 | United States | |||
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|
| Hallandale |
| Florida |
| 33009 |
| United States |
| St. Petersburg | Florida | 33709 | United States |
| Atlanta | Georgia | 30308 | United States |
| Long Branch | New Jersey | 07740 | United States |
| New York | New York | 10032 | United States |
| Bennington | Vermont | 05201 | United States |
| ID | Term |
|---|---|
| D000544 | Alzheimer Disease |
| ID | Term |
|---|---|
| D003704 | Dementia |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D024801 | Tauopathies |
| D019636 | Neurodegenerative Diseases |
| D019965 | Neurocognitive Disorders |
| D001523 | Mental Disorders |
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| ID | Term |
|---|---|
| C581984 | SAM-531 |
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