The Effect of High Fat Diet on the Pharmacokinetics of AD16 Tablets in Healthy Chinese Adult Subjects
NCT ID: NCT05787041
Last Updated: 2023-12-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
16 participants
INTERVENTIONAL
2019-06-14
2019-12-14
Brief Summary
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Compared with fasting administration, a high-fat diet reduced the rate of AD16 tablet absorption in healthy adult subjects and had no effect on overall exposure to AD16.
The elimination and distribution characteristics of AD16 in vivo were similar under the conditions of feeding and fasting administration.
A single dose of AD16 tablets after fasting and high fat diet showed good safety.
Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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High-fat diet group
A single dose of AD16 tablets was taken orally after a high fat diet
high-fat diet group（AD16 20mg）
AD16 was administered with 240 mL water 30 minutes after the subjects ate a high-fat, high-calorie food.
Fasting group
A single dose of AD16 tablets was taken orally under fasting conditions
fasted group（AD16 20mg）
Subjects took AD16 on an empty stomach and fasted within 4 hours after taking the drug.
Interventions
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high-fat diet group（AD16 20mg）
AD16 was administered with 240 mL water 30 minutes after the subjects ate a high-fat, high-calorie food.
fasted group（AD16 20mg）
Subjects took AD16 on an empty stomach and fasted within 4 hours after taking the drug.
Eligibility Criteria
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Inclusion Criteria
2. Weight ≥50kg (male) or ≥45kg (female), and body mass index (BMI) of 19-24kg/m2 (including the boundary values at both ends).
3. Have fully understood this study, voluntarily participated in it, and signed the Informed Consent.
4. Subjects are able to communicate well with researchers and complete the study according to protocol.
5. The subjects were deemed to be in good health based on physical examination, medical history, vital signs, electrocardiogram, chest X-ray, abdominal ultrasound, and laboratory tests.
6. Subject (including partner) is willing to have no pregnancy plan for the next 30 days (female subject) or 90 days (male subject) and is willing to use effective contraception.
Exclusion Criteria
2. The patient has symptoms or related history of any serious disease, including but not limited to heart, liver, kidney, or other acute or chronic digestive tract or respiratory tract diseases, as well as diseases of the blood, endocrine, neurological, psychiatric and other systems, or any other disease or physiological condition that can interfere with the study results.
3. A history of postural hypotension with frequent episodes.
4. A history of frequent nausea or vomiting due to any cause.
5. Any clear history of drug or food allergies, especially allergies to ingredients similar to the drugs in this study.
6. Have special dietary requirements and cannot comply with the uniform diet provided by the clinical research center.
7. Previous drug abuse history or positive urine drug screening during screening period.
8. Smokers who smoked more than 5 cigarettes a day in the 3 months before the test.
9. Heavy drinkers or regular drinkers in the 6 months prior to the study screening, who drank more than 14 units of alcohol per week (1 unit of alcohol ≈360 mL beer or 45 mL 40% spirits or 150 mL wine) or had a positive alcohol breath test during the screening period.
10. Excessive consumption of tea, coffee (more than 6 cups) and/or caffeinated beverages (more than 1L) per day.
11. Take food or drink rich in xanthine, grapefruit or alcohol, caffeine (e.g., dragon fruit, mango, grapefruit, chocolate, coffee or tea) within 48 hours before administration.
12. Surgical procedures, transfusions of blood or blood components in the month prior to study screening.
13. Blood loss or donation of more than 400 mL in the 2 months prior to screening.
14. Participated in other clinical studies and took experimental drugs within 3 months prior to study screening.
15. Study participants who had received any medication in the 28 days prior to screening.
16. Pregnant or lactating women or women who have had unprotected sex within 14 days.
17. Those unable to complete the study for other reasons or deemed unsuitable for inclusion by the researcher.
18 Years
45 Years
ALL
Yes
Sponsors
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Xiangya Hospital of Central South University
OTHER
South China Center For Innovative Pharmaceuticals
OTHER
Responsible Party
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Locations
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The Central South University Xiang Ya Hospital
Changsha, , China
Countries
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References
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Peng D, Xu S, Zou T, Wang Y, Ouyang W, Zhang Y, Dong C, Li D, Guo J, Shen Q, Hu X, Zhou W, Li X, Qin Q. Safety, tolerability, pharmacokinetics and effects of diet on AD16, a novel neuroinflammatory inhibitor for Alzheimer's disease: a randomized phase 1 study. BMC Med. 2023 Nov 23;21(1):459. doi: 10.1186/s12916-023-03126-9.
Other Identifiers
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SCCIP-AD16-2018-02
Identifier Type: -
Identifier Source: org_study_id