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Trials / Completed

CompletedNCT01623895

Pharmacogenetic Study in Patients Received Iron Chelating Agent

Status
Completed
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
Seoul National University Hospital · Academic / Other
Sex
All
Age
21 Years
Healthy volunteers
Not accepted

Summary

To investigate effect of genetic variations on the toxicities and find optimal target population, the investigators planned to analyze the genetic polymorphisms of UDP-glucuronosyltransferase.

Detailed description

Transfusion-associated iron overload induces systemic toxicity. Recently, deferasirox, a convenient long acting oral agent, has been introduced in clinical practice with promising efficacy. However, some patients experience drug-related toxicities and cannot tolerate it. To investigate effect of genetic variations on the toxicities and find optimal target population, we planned to analyze the genetic polymorphisms of UDP-glucuronosyltransferase 1A (UGT1A) subfamily, multi-drug resistance-associated protein 2 (MRP2) and breast cancer resistance protein (BCRP) among pediatric patients received deferasirox.

Conditions

Timeline

Start date
2007-12-01
Primary completion
2013-06-01
Completion
2013-06-01
First posted
2012-06-20
Last updated
2014-07-14

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01623895. Inclusion in this directory is not an endorsement.

Pharmacogenetic Study in Patients Received Iron Chelating Agent (NCT01623895) · Clinical Trials Directory