Chong Kun Dang applied for COVID-19 treatment
By An, Kyung-Jin | translator Choi HeeYoung
21.03.08 11:14:29
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The effect of improving symptoms and shortening the recovery period was confirmed in patients with severe high-risk groups
Discussions on exports with a number of foreign countries such as the UK, France, and Russia are in progress
Simultaneous application for phase 3 clinical trial plan for 600 severely ill patients
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Chong Kun Dang announced on the 8th that it has applied to the MFDS for approval of the conditional marketing authorization (CMA) and phase 3 clinical trial plan of Nafabelltan (Nafamostat) as a treatment for COVID-19 for patients with severe and high risk.Nafabelltan is a drug used as a therapeutic agent for acute pancreatitis and as an anticoagulant. Nafabelltan inhibits the proteolytic enzyme TMPRSS2, which is known to be involved in the cell penetration process of COVID-19. Chong Kun Dang confirmed the possibility of developing it as a COVID-19 treatment in a drug re-creation study by Institut Pasteur Korea, and has been promoting the development of COVID-19 treatment with Institut Pasteur Korea a
An, Kyung-Jin(kjan@dailypharm.com)
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