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Santersus AG, a privately held therapeutic apheresis company, announced today that their medical device product, NucleoCapture, has been granted designation as a Breakthrough Device by The Center for Devices and Radiological Health (CDRH) of the US Food and Drug Administration (FDA). The indication cited in the breakthrough designation is as an adjunctive treatment to antibiotics in patients with sepsis.
January 20, 2022
It was shown that circulating NETs might support Inflamm-ageing chronic low grade inflammation typical of ageing, being common biological factor responsible for the decline and the onset of disease in the elderly. At Santersus, we are investigating the use of NucleoCapture to prevent Inflamm-ageing and slow down functional decline in the elderly.
September 30, 2021
Santersus AG announces the successful completion of their first in human clinical trials relating to Sepsis and COVID-19.
This important publication reveals the profound impact of cell-free DNA clearance and its involvement in the survival of patients who suffer from severe SARS-CoV-2 infection. This obviously presents a novel therapeutic opportunity for our technology, NucleoCapture, which allows for selective removal of NETs from blood without compromising the defensive function of neutrophils.