NEW DELHI : Biocon Biologics has received DCGI approval for emergency use of CytoSorb to treat critical COVID-19 patients.
The US Food and Drug Administration (USFDA) had recently approved CytoSorb for emergency use in COVID-19 patients. Biocon Ltd.
announced on Wednesday that its subsidiary Biocon Biologics has received the Drugs Controller General of India's (DCGI) approval for an extracorporeal blood purification (EBP) device CytoSorb to reduce pro-inflammatory cytokines levels in confirmed COVID-19 patients admitted to the intensive care unit (ICU) with confirmed or imminent respiratory failure.
Biocon Biologics has been granted licence for emergency use of CytoSorb in public interest by the Indian health regulator to treat COVID-19