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  • Phase III clinical trial plan for Rimatil has been submitted
  • by Nho, Byung Chul | translator Choi HeeYoung | Jul 8, 2020 09:14am
Canadian pharmaceutical company submitted clinical approval plan to FDA on 30th of last month
Bucillamine, effective in COVID-19 patients
Introduced from Santen, Japan, verify safety and secure exclusive domestic sales rights
Chong Kun Dang added a clinical pipeline for COVID-19 treatment following Nafabeltan.

On the 18th of last month, Chong Kun Dang began the development of a COVID-19 treatment (clinical phase II) for its anticoagulant and acute pancreatitis treatment drug Nafabeltan (Nafamostat) on the 18th of last month.

It is estimated that the mechanism of Nafamostat inhibits protease TMPRSS2, which is known to play a major role in the cell invasion process of COVID-19, and shows several hundred times more antiviral efficacy in human lung cell experiments compared to Remdesivir.

On the 30th, IND application for Rimatil (Bucillamine) which is marketed as a rheumatoid arthritis treatment was submitted to the FDA.

The Phase
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