Case Control Study of Pharmacogenomic Factors Associated With Hepatocellular Injury Following Exposure to Lapaquistat Acetate

NCT00890448 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 66

Last updated 2012-05-24

No results posted yet for this study

Summary

The purpose of this study is to examine the genetic contribution to the mechanism of lapaquistat acetate- induced hepatic abnormalities.

Conditions

  • Toxicity

Interventions

OTHER

Pharmacogenomic whole blood sampling

10 mL, whole blood, one sample on Visit 2

Sponsors & Collaborators

Principal Investigators

  • Medical Director · Takeda

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-05-31
Primary Completion
2010-05-31
Completion
2010-05-31

Countries

  • United States
  • Argentina
  • Canada
  • Chile
  • Czechia
  • Finland
  • Germany
  • Latvia
  • Netherlands
  • Poland
  • Russia
  • Slovakia
  • South Africa
  • United Kingdom

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00890448 on ClinicalTrials.gov