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Search / Trial NCT00973986

Effect of CYP3A Genetic Polymorphisms on the Pharmacokinetics of Atorvastatin

Launched by LIUHUAQIAO HOSPITAL · Sep 8, 2009

Trial Information

Current as of July 25, 2025

Completed

Keywords

Atorvastatin Genetic Polymorphisms Coronary Heart Disease Pharmacokinetics Cyp3 A

ClinConnect Summary

Large variability exists in the individual response to statins. CYP3A polymorphisms likely contribute to variable response to those drugs primarily metabolized by CYP3A including atorvastatin.

Gender

MALE

Eligibility criteria

  • Inclusion Criteria:
  • Subjects must demonstrate their willingness to participate in the study and comply with its procedures by signing a written informed consent.
  • Subjects must be \>=35 years and \<=70 years of age.
  • Subjects must have an LDL-C concentration \>=2.6 mmol/L and TC concentration \>=4.14 mmol/L
  • Body mass index (BMI) must be within the range of 19 to 30 for patients.
  • * Subjects must have documented coronary heart disease with one or more of the following features:
  • Documented stable angina (with evidence of ischemia on exercise testing)
  • History of myocardial infarction
  • History of percutaneous coronary intervention (with or without stent placement)
  • Documented history of unstable angina or non-Q wave myocardial infarction.
  • Exclusion Criteria:
  • Diabetes and endocrine or metabolic disease.
  • Congestive heart failure defined by New York Heart Association (NYHA) as Class III or IV.
  • Uncontrolled cardiac arrhythmia.
  • Uncontrolled hypertension (Systolic BP \>160 mm Hg and/or Diastolic BP \>100 mmHg on two consecutive measurements).
  • Liver or kidney disease confirmed by abnormal lab values or function.
  • Smokers who report cigarette use of more then 10 cigarette per day.
  • Subjects who consume \>2 alcoholic drinks a day. (A drink is: a can of beer, glass of wine, or single measure of spirits).
  • Known human immunodeficiency virus (HIV) positive.
  • Cancer.
  • * Subjects who are on any of the following concomitant medications:
  • Medications that are potent inhibitors of CYP3A, including cyclosporine, itraconazole, fluconazole, and ketoconazole, erythromycin or clarithromycin, nefazodone, protease inhibitors,mibefradil and large amounts of grapefruit juice (\>1 quart/day).
  • Lipid-lowering agent: niacin (\>200 mg/day) taken within 5 weeks, fibric acid derivatives taken within 8 weeks.

About Liuhuaqiao Hospital

Liuhuaqiao Hospital is a leading healthcare institution dedicated to advancing medical research and improving patient outcomes through innovative clinical trials. With a commitment to high standards of ethical practices and patient safety, the hospital collaborates with a multidisciplinary team of healthcare professionals to conduct rigorous studies across various therapeutic areas. By leveraging state-of-the-art facilities and a patient-centered approach, Liuhuaqiao Hospital aims to contribute valuable insights to the medical community, ultimately enhancing treatment options and fostering advancements in healthcare.

Locations

Guangzhou, Guangdong, China

Patients applied

0 patients applied

Trial Officials

Zhao Shujin, PhD

Study Director

Guangzhou General Hospital of Guangzhou Military Command

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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