It is being offered as a testing service through ProterixBio's high-complexity clinical testing laboratory.
Validation results demonstrated a Positive Percent Agreement of 100% for samples acquired >15 days after symptoms onset and a Negative Percent Agreement of 100% in negative controls acquired prior to the pandemic.
The SARS-COV-2 IgG Antibody test detects antibodies that bind to the Receptor Binding Domain of the spike protein of the SARS-CoV-2 virus.
The assay output is numerical value related to the levels antibodies present in the sample that can be used to better understand the course of an individual's immune response.
The RBD is the region of the spike protein that binds to the ACE-2 receptor of host cells and facilitates virus entry.
Studies have shown that antibodies to the RBD are associated with neutralizing activity, which plays a critical role in the adaptive immune response and the potential development of immunity. Several of the leading candidate SARS-CoV-2 vaccine designs incorporate sequences of the RBD.
Serology assays are an important tool to support the development of vaccines, convalescent plasma and hyperimmune products as well as back-to-work/school programs and public health surveillance.
ProterixBio's high-complexity clinical testing laboratory is capable of analyzing 1,000's of samples per day and is further scaling capacity to meet increasing demand.
The SARS-CoV-2 IgG Antibody test meets or exceeds the requirements for COVID-19 serology assays set by the US Food and Drug Administration. ProterixBio has notified and submitted validation results to the FDA.
ProterixBio is a licensed high-complexity clinical testing laboratory that develops and commercializes diagnostic solutions that address critical unmet needs in population health and chronic care.
An area of focus has been vulnerable populations such as those with chronic obstructive pulmonary disease, diabetes and cardiovascular disease.
The company has developed algorithms utilizing combinations of blood-based biomarkers for identifying individuals at high risk for severe outcomes.
ProterixBio maintains a rigorous approach to test development that includes collaborating with leading academic medical centers and validating assays in large, carefully curated cohorts. ProterixBio is headquartered and operates a laboratory in Billerica, MA.
Tempus announces receipt of FDA clearance for AI pulmonary hypertension detection product
European Commission grants orphan designation for Lundbeck's asedebart
Hanmi Pharm enters exclusive licensing deal with Genentech for obesity therapy HM17321
PTC to acquire BLA-stage ST-920 Fabry disease programme
Olio Labs reveals study demonstrating AI-driven in vivo platform can predict clinical trial outcomes
Mezzion Pharma Co reports positive results from new in vivo study of udenafil
Incyte's Opzelura approved in European Union for moderate atopic dermatitis
American Regent recalls one lot of Papaverine Hydrochloride Injection due to particulate matter
Galmed announces breakthrough development of SCD1 inhibitor Aramchol for cardiac fibrosis