Clinical Performance Evaluation of the NeuMoDx™ EBV Quant Assay 2.0 in Immunocompromised Transplant Patients

CompletedOBSERVATIONAL
Enrollment

1,070

Participants

Timeline

Start Date

August 31, 2022

Primary Completion Date

December 31, 2023

Study Completion Date

March 15, 2024

Conditions
EBV Viremia
Interventions
DIAGNOSTIC_TEST

NeuMoDx EBV Quant 2.0 Assay

The NeuMoDx™ EBV Quant Assay 2.0 is an automated in vitro nucleic acid amplification test for the quantification of Epstein-Barr virus (EBV) DNA in EDTA plasma from immunocompromised transplant patients. Transplant patients are screened for EBV viral load as part of their standard of care. The remaining samples from these in vitro diagnostic nucleic acid amplification tests (NAAT) will be analyzed using the NeuMoDx EBV Quant Assay 2.0 to quantify EBV DNA in EDTA plasma. That result will be compared to a comparator in vitro diagnostic assay to evaluate the performance of the NeuMoDx EBV Quant 2.0 assay.

Trial Locations (1)

M130BH

QIAGEN Gaithersburg, Inc., Manchester

All Listed Sponsors
lead

QIAGEN Gaithersburg, Inc

INDUSTRY