Ultra sensitive MRD testing in Blood for Multiple Myeloma patients

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® is a Laboratory Developed Test (LDT) validated for clinical use, being offered by Corgenix, US-based Clinical Laboratory, 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's poster at ADLM Chicago 2024 received 2 awards!

Our poster "Next Generation monitoring: M-inSight® Clinical Application in Multiple Myeloma" was awarded the "Mass Spectrometry and Separation Science Division Abstract" award and the "Personalized Medicine Division Abstract" award during ADLM Chicago 2024.
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M-INSIGHT®

M-inSight® provides deeper
insights into Multiple Myeloma monitoring

High sensitivity, at MRD level

Because deeper response require more sensitive testing, M-inSight® has been developed to detect very low level of M-protein. M-inSight® sensitivity in blood is equivalent to MRD evaluation in bone marrow and 1,000 x more sensitive than IFE. The Clonotypic peptides targeting avoids the interference with the polyclonal background and with therapeutic monoclonal antibodies.

Treatment performance monitoring

M-inSight® tracks low level disease over time, monitors kinetics and depth of response and detects early progression of the disease. Thanks to its non-invasive sampling, clinicians can ask for M-inSight® as frequently as needed for a dynamic monitoring of MRD.

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.