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Completed

NCT Number: NCT00973986

Effect of CYP3A Genetic Polymorphisms on the Pharmacokinetics of Atorvastatin

The aim of the study is to investigate the effects of CYP3A polymorphisms on the pharmacokinetics of Atorvastatin in Chinese subjects with coronary heart disease.

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Key information

Age range

35 year–65 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Guangzhou General Hospital of Guangzhou Military Command

Guangzhou, Guangdong, 510010, China

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

atorvastatin

Drug

The subjects will receive atorvastatin (20 mg single dose) orally with approximately 240 ml of water. Blood samples(4 mL) will be taken prior to dosing and at 0.33, 0.66, 1, 1.5, 2, 2.5, 3, 4, 6, 9, 12, 24 and 48 h after drug administration.

Other names: Lipitor, Atorvastatin Calcium Tablets

Primary outcomes

  1. Compare the area under the plasma concentration versus time curve (AUC) and Area under the plasma concentration versus time curve (AUC) of atorvastatin with different CYP3A4*1G genotypes.

    Time frame: 48h

Secondary outcomes

  1. The pharmacokinetics of atorvastatin in Chinese with coronary heart disease.

    Time frame: 48h

Sponsors and collaborators

Lead sponsor

Liuhuaqiao Hospital

Other

Collaborators

  • Guangdong Province, Department of Science and Technology

Registry information

Official study title

Study the Effect of CYP3A Genetic Polymorphisms on the Pharmacokinetics of Atorvastatin in Chinese Subjects With Coronary Heart Disease

Acronym: ECGPPA

Important dates

Study start
2009
Primary completion
2010
Study completion
2011
First posted
Sep 9, 2009
Registry last updated
Nov 29, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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