A Study to Investigate the Food Effect on the Pharmacokinetics of Ensartinib Capsules in Chinese Healthy Volunteers.
Study Details
Study Description
Brief Summary
The main objective of this study is to evaluate the Effect of Food on the Pharmacokinetics of Ensartinib Capsules.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1 |
Detailed Description
The main objective of this study is to evaluate the Effect of Food on the Pharmacokinetics of Ensartinib Capsules in Chinese Healthy Volunteers. In addition, the safety of Ensartinib Capsules in Chinese Healthy Volunteers who with High-fat meal or fasting state will also be evaluated.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Period 1: fed control → Period 2: fasted control Period 1: administration of Ensartinib 225mg at 7:30am, 30 minutes after the breakfast；Period 2: administration of Ensartinib 225mg at 7:30am, without the breakfast |
Drug: Ensartinib with fed or fasting
The two groups of subjects were given an equal dose of Ensartinib capsules (225 mg) after a single cross-over fasting or high-fat high-calorie diet in two different test cycles to examine the effect of food on the pharmacokinetics of Ensartinib.
|
| Experimental: Period 1: fasted control → Period 2: fed control Period 1: administration of Ensartinib 225mg at 7:30am, without the breakfast；Period 2: administration of Ensartinib 225mg at 7:30am, 30 minutes after the breakfast |
Drug: Ensartinib with fed or fasting
The two groups of subjects were given an equal dose of Ensartinib capsules (225 mg) after a single cross-over fasting or high-fat high-calorie diet in two different test cycles to examine the effect of food on the pharmacokinetics of Ensartinib.
|
Outcome Measures
Primary Outcome Measures
- Peak plasma concentration (Cmax) of Ensartinib [pre-dose(30minute),30min,1,1.5,2,2.5,3,3.5,4,4.5,5,6,8,12,24,36,48,72,96,120hour]
The effect of food on Cmax after high fat diet and fasting Blood sampling over a 120 hour period post dose in all dosing sessions
- Area under the plasma concentration versus time curve (AUC) of Ensartinib [pre-dose(30minute),30min,1,1.5,2,2.5,3,3.5,4,4.5,5,6,8,12,24,36,48,72,96,120hour]
The effect of food on AUC after high fat diet and fasting Blood sampling over a 120 hour period post dose in all dosing sessions
- Time of maximum concentration（Tmax）of Ensartinib [pre-dose(30minute),30min,1,1.5,2,2.5,3,3.5,4,4.5,5,6,8,12,24,36,48,72,96,120hour]
The effect of food on Tmax after high fat diet and fasting Blood sampling over a 120 hour period post dose in all dosing sessions
- Half life（T1/2）of Ensartinib [pre-dose(30minute),30min,1,1.5,2,2.5,3,3.5,4,4.5,5,6,8,12,24,36,48,72,96,120hour]
The effect of food on T1/2 after high fat diet and fasting Blood sampling over a 120 hour period post dose in all dosing sessions
Secondary Outcome Measures
- Percentage of adverse events [From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 months]
Percentage of adverse events as assessed by CTCAE v4.0
Eligibility Criteria
Criteria
Inclusion Criteria:
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age: 20 - 45 years;
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sex: male and female;
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body weight: Male ≥ 50 kg,female ≥ 45 kg, body mass index BMI (weight (kg)/height 2 (m2)) between 19-26 kg/m2 (including border);
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Healthy as judged by the investigator/subinvestigator based on the results of physical examinations and all lab tests;
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written informed consent;
Exclusion Criteria:
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Received any investigational drugs within 14 days before the screening test;
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Donated 200 mL of whole blood within 30 days before the screening test,or Donated 200 mL of whole blood during the study or within 30 days after completion of the study;
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Females who are lactating, pregnant, potentially child-bearing, or willing to get pregnant during the study period;
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History of drug or food allergies;
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Abnormal blood pressure or pulse，Abnormal laboratory tests;
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Participated in other clinical trials within 3 months before screening;
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Smoking and drinking within 3 months before screening or test results of smoke, alcohol, and drug abuse are positive;Positive for HBsAg, Hepatitis C virus (HCV) antibody, HIV antibody or syphilis antibody;Clinically apparent disease/infection within 1 month before screening;
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Positive for HBsAg, Hepatitis C virus (HCV) antibody, HIV antibody or syphilis antibody;
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Clinically apparent disease/infection within 1 month before screening;
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | The 1st Phase Clinical Research Center of the Second Affiliated Hospital of Zhejiang University Medical College | Hangzhou | Zhejiang | China | 311009 |
Sponsors and Collaborators
- Betta Pharmaceuticals Co., Ltd.
Investigators
- Study Chair: zourong ruan, the Second Affiliated Hospital of Zhejiang University Medical College
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- BTP-44313