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The bioequivalence study of atorvastatin and the effect of transporters, metabolic enzymes and food on pharmacokinetics of atorvastatin

The bioequivalence study of atorvastatin and the effect of transporters, metabolic enzymes and food on pharmacokinetics of atorvastatin

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15006175
Enrollment
Unknown
Registered
2015-04-01
Start date
2015-04-10
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hyperlipidaemia

Interventions

Four groups:Atorvastatin or Lipitor is administrated after taking food versus fasting

Sponsors

Institute of Clinical Pharmacology, Central South University
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Sex: male; 2. Age: 18~45 years old, the age difference in the same group is not more than 10 years; 3. weight is greater than or equal to 50 kg, the body mass index (BMI) in 19~24 kg/m2 (BMI= body weight (kg)/height 2 (M2)), including the boundary value; 4. On the basis of a physical examination, medical history, vital signs, electrocardiogram and clinical laboratory test results, the researchers believe that the subjects in good health, heart, liver, kidney, gastrointestinal, neurological, psychiatric disorders and metabolic disorders and other medical history; the complete physical examination and vital signs, body temperature, heart rate and blood pressure check display, respiratory conditions and laboratory examination including ECG, blood routine, urine routine, liver and kidney function, blood glucose, blood lipid, serum electrolytes, myocardial enzyme, blood coagulation function, blood transfusion, the laboratory examination showed no abnormality or no clinical significance of abnormal (to the clinician's judgment shall prevail); 5. subjects must be informed consent before the trial, and voluntarily signed the written informed consent; 6. subjects can communicate with the researchers and be able to finish the study in accordance with the protocol.

Exclusion criteria

Exclusion criteria: 1. allergic or known to this product or any of its accessories allergy; 2. circulating system, endocrine system, nervous system, digestive system, respiratory system, hematology, immunology, psychiatry and abnormal metabolism of any clinical history of serious illness or to interfere with the test results of any other disease or physical condition; 3. undergoing gastrointestinal problems, spasm, gastrointestinal ulcer, urinary infarction, intestinal obstruction, ureteral spasm, biliary tract disease, depression or liver disease; 4. with can affect drug absorption or metabolism of gastrointestinal and liver, kidney disease; 5. test within 4 weeks before treated with surgical operation; 6. known to affect the venous blood of serious hemorrhage factors; 7. with malignant tumor of history; 8. test 30 days before the use of any inhibition or induction of hepatic drug on drug metabolism (such as: inducing agent, barbiturates, phenytoin, C Masi Bing, glucocorticoid, Omeprazole; inhibitor SSRI antidepressants, cimetidine, diltiazem, macrolides, nitroimidazole, sedative hypnotics, Vera Pammy, fluoroquinolones, antihistamine) who; Abnormal ECG; 9. with clinical significance of vital signs) or abnormal (systolic blood pressure lower than 90 mmHg or higher than 140 mmHg, lower than 50 mmHg or higher than 90 mmHg diastolic blood pressure; heart rate less than 50 BPM or more than 100 BPM); 10. HIV, hepatitis B surface antigen, hepatitis or syphilis antibody positive; 11. alcoholic or 6 months before the test current drinkers, drinking more than 14 units of alcohol per week (1 units of =360 mL beer or 45 mL alcohol content of 40% spirits or 150 mL Wine); 12. smoker or test before 3 months of daily smoking more than 5 cigarettes; 13. drug abusers or test 3 months before the use of soft drugs (such as: marijuana) or test 1 years ago taking hard drugs (such as: cocaine, PCP etc.) who; 14. any food allergies or food to have special requirements, can not comply with the uniform diet; 15. every day drinking too much tea, Coffee and / or caffeinated beverages (more than 8 cups, 1 cup of =250 ml) who; 16. test 14 days before taking any drugs; 17. test in the 3 months before taking any drug clinical trials or in any drug clinical trials; 18. test 3 months before the blood donation or be sampled as the subjects; 19. subjects may be because of other reasons not to complete this study or research that should not be included in the party.

Design outcomes

Primary

MeasureTime frame
Concentration of atorvastatin and its metabolites in plasma;

Countries

China

Contacts

Public ContactDongsheng Ouyang
ouyangyj@163.com+86 13307313736

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026