Sequenta, Inc.'s ClonoSIGHT MRD Test Can Detect Relapse Of Diffuse Large B-Cell Lymphoma More Than Seven Months Before CT Scan

NEW ORLEANS--(BUSINESS WIRE)--Sequenta, Inc. today announced that researchers from the National Cancer Institute (NCI) will present data showing that in the first five years post-treatment, the company’s sequencing-based minimal residual disease (MRD) assay can detect relapse of diffuse large B-cell lymphoma (DLBCL) a median of 7.4 months prior to when the disease is detected via CT scan. Sequenta’s recent announcement of the commercial launch of the ClonoSIGHT test for use in DLBCL patients is based on this clinical validation data, which will be presented at the 55th annual meeting of the American Society of Hematology (ASH).

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