RecruitingNCT03568266

Pharmacogenomics of Asparaginase Induced Hepatotoxicity

Pharmacogenomics of Age-Specific, Asparaginase-Induced Hepatotoxicity in Patients With Acute Lymphoblastic Leukemia


Sponsor

University of Southern California

Enrollment

500 participants

Start Date

May 22, 2018

Study Type

OBSERVATIONAL

Conditions

Summary

This pilot trial studies the impact of genetic information on developing liver damage caused by asparaginase in participants with newly diagnosed acute lymphoblastic leukemia. Testing saliva samples may help doctors find certain genetic markers that may predict whether participants will tolerate asparaginase, which is given as part of clinical care for acute lymphoblastic leukemia.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study investigates why some patients with a blood cancer called acute lymphoblastic leukemia (ALL) develop liver damage (hepatotoxicity) from a standard chemotherapy drug called asparaginase, by looking at differences in patients' genes that might explain this reaction. **You may be eligible if...** - You have been newly diagnosed with acute lymphoblastic leukemia (ALL) and have not yet started treatment for it - You are receiving asparaginase as part of your cancer treatment plan - You are able to understand and sign an informed consent form - For retrospective (past patient) enrollment: you received asparaginase between 2012 and 2017 and are a current patient at the University of Southern California **You may NOT be eligible if...** - You are unable to give informed consent Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREBiospecimen Collection

Undergo collection of saliva


Locations(1)

USC / Norris Comprehensive Cancer Center

Los Angeles, California, United States

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NCT03568266


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