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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

 ¡ãNafabelltan

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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