The announcement follows the recent launch of Babson's IgG serology test, which yielded 93.2% sensitivity and 100.0% specificity in its clinical performance evaluation and has been submitted to the FDA for Emergency Use Authorization.
The longitudinal research study is designed to measure the adaptive immune response to SARS-CoV-2 by following individuals over a two-year period.
The initial phase of the study begins with 200 COVID-19 positive individuals, including patients and health care workers from UT Health Austin, the clinical practice of Dell Med. Babson will provide serology testing services as part of the collaboration.
The research is designed to inform the diagnosis and treatment of COVID-19 infections as well as guide the allocation of critical medical resources.
Babson's pipeline of fully automated serology assays are heterogeneous immunoassays analyzed on high-throughput commercial analyzers in the company's CLIA-certified, CAP-accredited, high-complexity clinical laboratory located in Austin.
The research initiative is a continuation of the collaborative relationship Babson and Dell Med have maintained since Babson became one of the first companies to take up residence within Dell Med's WorkSpaces, part of the Texas Health CoLab, a center for health product innovation entrepreneurship aligned with the medical school's mission.
Babson also initiated its own clinical study to further validate its serology testing services. To learn more about Babson's serology testing services and clinical studies.
Babson Diagnostics aims to bring diagnostic blood testing to the retail pharmacy counter, making it easier, faster, and more pleasant for customers to routinely monitor and improve their health.
Babson's proprietary technological ecosystem is designed to deliver accurate diagnostic results with a more human experience.
Akeso presents positive results from registrational Phase III study of ivonescimab
FDA grants Priority Review to Genentech's Enspryng for MOGAD
Seismic Pharmaceuticals enrols first patient in istaroxime global Phase 3 trial in cardiogenic shock
BioEdge Research Labs advances transparency in research compound documentation
Insilico Medicine doses first patient in Phase III trial of rentosertib
BridgeBio reports exploratory PROPEL 3 data showing wider clinical trends for oral infigratinib
Tyra Biosciences declares positive Phase 2 results for oral dabogratinib in bladder cancer
Harbour BioMed partner raises USD225m to advance neoadjuvant immuno-oncology therapy porustobart
Kazia Therapeutics doses first patient in paediatric AT/RT study
Fusion Antibodies secures Canadian patent for OptiMAL
Revvity to acquire Human Cell Design to expand metabolic disease drug discovery capabilities
Biophytis expands BIO101 obesity study to assess weight regain
THX Pharma secures European patent for Batten-1 in juvenile Batten disease
Orphalan commences Phase 3 study of trientine therapy in Wilson disease