Skip to main content
Premium Trial:

Request an Annual Quote

Myriad RBM, Sanofi Partner to Identify CV Biomarkers in Diabetes Patients

NEW YORK (GenomeWeb) – Myriad RBM announced today that it has signed an agreement to help Sanofi measure cardiovascular risk biomarkers in the blood samples of patients in a Phase III trial of its type II diabetes therapy lixisenatide.

Last year, Sanofi released data from the study — called Evaluation of Lixisenatide in Acute Coronary Syndrome, or ELIXA — showing that the drug did not improve cardiovascular outcomes for the trial's 6,000 diabetes patients who had been deemed high risk after having recently had a spontaneous acute coronary syndrome event. Lixisenatide treatment did not increase cardiovascular risk in these patients either.

Under the terms of their agreement, Sanofi will provide Myriad RBM with roughly 5,300 serum samples from the ELIXA trial. Myriad RBM will analyze these samples using its CustomMAP platform — essentially a version of its immunoassay-based DiscoveryMAP platform that uses pre-selected biomarkers — in order to measure protein biomarkers predictive of cardiovascular and microvascular risk in type II diabetes.

Financial terms of the deal were not disclosed.

The arrangement follows a 2012 partnership between the companies to identify protein biomarker  patterns in serum samples from a Sanofi study testing its long-lasting insulin Lantus (insulin glargine) in pre-diabetic and early type II diabetes patients. They identified a series of protein biomarkers associated with cardiovascular events or death in such patients, which were then confirmed using the CustomMAP platform.

"In prior studies, we demonstrated the power of DiscoveryMAP to identify panels of biomarkers that have important diagnostic and prognostic applications for people at a higher risk of a cardiovascular event," Myriad RBM President Ralph McDade said in a statement. "This new agreement with Sanofi will expand upon that experience. Our ultimate goal is to provide accurate estimates of the risk of a future cardiovascular event in patients so that drug developers and physicians can tailor care and achieve better health outcomes."
The Scan

Positive Framing of Genetic Studies Can Spark Mistrust Among Underrepresented Groups

Researchers in Human Genetics and Genomics Advances report that how researchers describe genomic studies may alienate potential participants.

Small Study of Gene Editing to Treat Sickle Cell Disease

In a Novartis-sponsored study in the New England Journal of Medicine, researchers found that a CRISPR-Cas9-based treatment targeting promoters of genes encoding fetal hemoglobin could reduce disease symptoms.

Gut Microbiome Changes Appear in Infants Before They Develop Eczema, Study Finds

Researchers report in mSystems that infants experienced an enrichment in Clostridium sensu stricto 1 and Finegoldia and a depletion of Bacteroides before developing eczema.

Acute Myeloid Leukemia Treatment Specificity Enhanced With Stem Cell Editing

A study in Nature suggests epitope editing in donor stem cells prior to bone marrow transplants can stave off toxicity when targeting acute myeloid leukemia with immunotherapy.