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AC-1202 (Ketasyn) is a nutritional beverage currently being studied in neurodegenerative conditions including Alzheimer's disease. The current study is a randomized, open-label trial to compare the safety, tolerability, and PK profiles of 3 formulations of Ketasyn administered on a daily basis for 14 days, with and without a 7-day titration period, in normal, healthy elderly volunteers.
Sixty healthy, elderly volunteers between the ages of 55 and 85 will be enrolled at one of four clinical sites in the Tampa/St. Petersburg area. Subjects with a history of GI inflammatory conditions (e.g., IBS or diverticulitis) or other clinically significant abnormalities will be excluded from enrollment. Subjects will be randomized to one of two dosing regimens (with or without a 7-day titration period) and to one of three formulations of Ketasyn containing the identical amount of active ingredient, but different amounts of proteins and carbohydrates. Subjects assigned to Group 1 will receive 10 grams active ingredient daily on Days 1-7, followed by a daily dose of 20 grams active ingredient on Days 8-14. Subjects assigned to Group 2 will receive 20 grams active ingredient on Days 1-14. All subjects will have clinic visits on Day 1 and 14; subjects assigned to Group 1 will also have a clinic visit on Day 8. Subjects will fast prior to each clinic visit and have vital signs and routine lab tests performed prior to dosing. A standard breakfast will be served along with the study product, following which blood samples will be collected for product concentration levels.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | 10 gram x 7 days, then 20 gram x 7 days active ingredient of original formulation |
| |
| 2 | 20 grams x 14 days active ingredient of original formulation |
| |
| 3 | 10 grams x 7 days; then 20 grams x 7 days of low protein formulation |
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| 4 | 20 grams x 14 days of low protein formulation |
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| 5 | 10 grams x 7 days; then 20 grams x 7 days of high protein formulation |
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| 6 | 20 grams x 14 days of high protein formulation |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ketasyn | Other | 10g for 7 days, 20g for 7 or 14 days |
|
| Measure | Description | Time Frame |
|---|---|---|
| Plasma peak concentration levels and AUC | two weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence and severity of adverse events | 3 weeks |
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Inclusion Criteria:
Exclusion Criteria:
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Healthy elderly male and female subjects 55 - 85 years of age
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| Name | Affiliation | Role |
|---|---|---|
| Lauren Costantini, PhD | Cerecin | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Meridien Research Center | St. Petersburg | Florida | 33709 | United States |
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| ID | Term |
|---|---|
| D000544 | Alzheimer Disease |
| ID | Term |
|---|---|
| D003704 | Dementia |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
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plasma beta-hydroxybutyrate
| D024801 |
| Tauopathies |
| D019636 | Neurodegenerative Diseases |
| D019965 | Neurocognitive Disorders |
| D001523 | Mental Disorders |