Ultra sensitive, Personalized MRD testing in Blood

M-inSight® is a Blood test that tracks very low level of M-protein, the biomarker secreted by the cancer cells in Multiple Myeloma. M-inSight® technology is based on Clonotypic Peptides Mass Spectrometry.

M-inSight® is now available

M-inSight® has been validated for clinical use. This is a Laboratory Developed Test (LDT) being offered by Corgenix Clinical Laboratory, a CLIA certified, CAP accredited, high complexity clinical laboratory.

MRD monitoring in blood is now possible!

MRD is a powerful tool for prognosis. MRD negativity is associated with better outcomes for the patients. Novel techniques measuring MRD with a simple blood draw are less invasive for the patients.

Sebia offers powerful tools for the Myeloma Patient's Journey

Sebia is the only global partner covering the continuum of M-Protein Testing from initial detection to MRD.

Sebia launches
M-inSight®, a test for monitoring multiple myeloma patients

Corgenix, a Sebia Group company, CAP/CLIA clinical laboratory, positions Sebia to globally commercialize M-inSight®, a novel non-invasive liquid biopsy assay for Minimal Residual Disease (MRD) monitoring in multiple myeloma
decoration
M-INSIGHT®

M-inSight® provides deeper
insights into Multiple Myeloma monitoring

Deeper sensitivity

Because deeper response require more sensitive testing, M-inSight® has been developed to detect very low levels of M-protein. M-inSight® on blood is at least as sensitive as the latest generation of MRD evaluation performed on bone marrow. The Clonotypic peptides targeting avoids the interference with the polyclonal background, leading to a ultra sensitive test.

Disease tracking

M-inSight® tracks low level disease over time and provides deeper insights into MM monitoring : kinetics of response, sustained MRD negativity monitoring and early progression detection. Thanks to its non-invasive sampling, clinicians can ask for M-inSight® as frequently as needed compared to bone marrow-tests that are not suitable for dynamic MRD monitoring.

Personalized

The monoclonal Ig clone signature is unique and harbors multiple mass spectrometry-suitable clonotypic peptides for each patient with Multiple Myeloma. M-inSight® is able to detect clonotypic peptides coming from different clones.

Non invasive

M-inSight® can monitor MRD with a simple blood draw. This is a major improvement compared to bone marrow – MRD testing that present critical limitations: require invasive and painful bone marrow aspirate, provide limited timepoints and introduce the risk of false negative results due to tumor heterogeneity.
PRODUCT INQUIRY

M-inSight® has been validated for clinical use

M-inSight® is a Laboratory Developed Test (LDT) being offered by Corgenix Clinical Laboratory, a CLIA certified, CAP accredited, high complexity clinical laboratory.