Method Comparison of Ionify ISD and MPA Assays on the Cobas i 601 Analytical Unit

What is the Purpose of this Study?

The purpose of this study is to evaluate the performance of Roche assays (laboratory tests used to measure medication levels in the blood) on the cobas i601 analytical unit (a laboratory instrument used to analyze blood samples) and compare the results with currently used standard testing methods. Participants will be asked to provide a blood sample for research purposes. The samples will be shipped to a laboratory and tested on the i601 analytical unit and compared to results obtained from routine laboratory methods. Participants will be organ transplant recipients who are currently receiving immunosuppressive therapy. The study specifically involves patients who are receiving therapies such as tacrolimus, cyclosporine, sirolimus, everolimus, and/or mycophenolic acid following heart, liver, or kidney transplantation.


Eligibility

Not Available


Where can I participate?

Beverly


What is the full name of this clinical trial?

Method Comparison of Ionify ISD Assays, MPA, and MPAG on the Cobas i601 Analytical Unit

Study Details
Disease Type/Condition

Other

Principal Investigator

Yang, Ju Dong

Age Group

Adult

Phase

N/A

IRB Number

STUDY00004287


How do I learn more about this study?
Email
clinicaltrials@cshs.org
Study Detail
Disease Type/Condition

Other

Principal Investigator

Yang, Ju Dong

Age Group

Adult

Phase

N/A

IRB Number

RD006873


Contact
Email
clinicaltrials@cshs.org