Editor: What To Know
- BioPorto notes it is designed to provide a qualitative result in under 10 minutes from a minimally invasive sample, and to be easily administered at the point of care, the test could provide a much-needed solution to help improve access to viral testing.
- If we achieve our goals, the new COVID test, for the detection of the active virus, will demonstrate the value of our gRAD platform for fast and flexible creation of lateral flow assays, but more importantly, it could help make a real difference in global efforts to slow the virus through broad-based testing.
- If these efforts are ultimately successful, the Company intends to request an Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA) and to apply for CE Mark, which could lead to product launch before the end of the year.
September 17, 2020
BioPorto Diagnostics A/S (BioPorto) and the University of Southern Denmark (SDU) announced in April 2020 a fast-track collaboration to create a rapid test for SARS-CoV-2, the virus that causes COVID-19. Leveraging SDU’s antibody expertise and BioPorto’s Generic Rapid Assay Device (gRAD) platform for the development of lateral flow assays, the collaboration envisioned developing an instrument-free, simple solution to test patients for SARS-CoV-2.
BioPorto notes it is designed to provide a qualitative result in under 10 minutes from a minimally invasive sample, and to be easily administered at the point of care, the test could provide a much-needed solution to help improve access to viral testing.
Preliminary analytical studies of the newly created SARS-CoV-2 antibodies, for the detection of the active virus, have shown promising results in testing against heat-inactivated virus. These antibodies are highly specific to the virus’s spike protein, which should potentially result in a higher clinical specificity when compared to other commercially available rapid tests. In continued development over the next several months, BioPorto plans to evaluate, optimize, and validate the test using a variety of different sample types from known-positive patients.
If these efforts are ultimately successful, the Company intends to request an Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA) and to apply for CE Mark, which could lead to product launch before the end of the year.
“The expedited development of a gRAD-based COVID-19 test and our promising analytical results have been very encouraging,” said Peter Mørch Eriksen, CEO of BioPorto. “In a short time, we have been able to develop a test and bring it to the clinical evaluation stage. If we achieve our goals, the new COVID test, for the detection of the active virus, will demonstrate the value of our gRAD platform for fast and flexible creation of lateral flow assays, but more importantly, it could help make a real difference in global efforts to slow the virus through broad-based testing.”
