National Active Surveillance Network and Pharmacogenomics of Adverse Drug Reactions in Children

NCT00414115 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 7000

Last updated 2026-05-01

No results posted yet for this study

Summary

The purpose of the study is (1) to identify and collect samples from children and adults who take drugs and have adverse drug reactions AND children and adults who take drugs and do not experience any adverse drug effects; (2) to determine if genetic differences between the two groups contribute to causing the adverse drug reactions; and (3) to develop patient specific drug dosing guidelines to prevent future adverse drug reactions. We also wish to compare the use of prescription drugs, medical and hospital services and vital statistics between BC participants who experience adverse drug reactions and those who do not.

Study hypothesis: Genetic differences may contribute to patients' response to drugs and may be responsible for adverse drug reactions.

Conditions

  • Adverse Drug Reaction (ADR)

Sponsors & Collaborators

  • Genome Canada

    collaborator OTHER
  • Genome British Columbia

    collaborator INDUSTRY
  • Child and Family Research Institute

    collaborator OTHER
  • Western University, Canada

    collaborator OTHER
  • Provincial Health Services Authority British Columbia

    collaborator OTHER
  • Health Canada

    collaborator OTHER_GOV
  • Canada Gene Cure

    collaborator UNKNOWN
  • Eli Lilly and Company

    collaborator INDUSTRY
  • Pfizer

    collaborator INDUSTRY
  • Merck Sharp & Dohme LLC

    collaborator INDUSTRY
  • Canadian Society of Clinical Pharmacology

    collaborator UNKNOWN
  • Canadian Institutes of Health Research (CIHR)

    collaborator OTHER_GOV
  • Canada Foundation for Innovation

    collaborator OTHER
  • British Columbia Clinical Genomics Network

    collaborator OTHER
  • University of British Columbia

    lead OTHER

Principal Investigators

  • Bruce Carleton, Pharm. D. · University of British Columbia

  • Michael Hayden, MD, Ph.D · University of British Columbia

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2005-08-31
Primary Completion
2029-03-31
Completion
2029-03-31

Countries

  • Canada

Study Locations

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Entities

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 NCT00414115 on ClinicalTrials.gov