Sun Pharma gets DCGI nod to initiate clinical trial with Nafamostat in Covid-19 patients
Nafamostat is approved in Japan for the improvement of acute symptoms of pancreatitis and the treatment of Disseminated Intravascular Coagulation (DIC)
Mumbai: Sun Pharmaceutical Industries Ltd. has announced that it has received approval from the Drugs Controller General of India (DCGI) to initiate a clinical trial with Nafamostat Mesilate in Covid-19 patients.
Nafamostat is approved in Japan for the improvement of acute symptoms of pancreatitis and the treatment of Disseminated Intravascular Coagulation (DIC).
A group of scientists from the University of Tokyo, Japan, and Leibniz Institute for Primate Research, Germany have recently demonstrated that Nafamostat, at very low concentrations, suppresses a protein (TMPRSS2) that the Covid-19 virus uses to enter human lung cells. Another group from Institut Pasteur, South Korea, also published data comparing antiviral efficacy of 24 drugs and Nafamostat, against SARSCoV-2 in in-vitro studies in human lung epithelial derived cells. In this research, Nafamostat was found to be the most potent drug and was able to inhibit virus entry at very low concentrations, consistent with findings from Japan and German labs.
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