Phase III clinical trials showed that the treatment significantly reduced deterioration of COVID-19 symptoms to severe levels and shortened recovery, the Ministry of Food and Drug Safety said in a statement on Friday.

The treatment lowered the rate of high-risk patients developing severe symptoms by 72% and shortened recovery by 4.12 days, the ministry said.

Celltrion said in a separate regulatory filing it plans to apply for emergency use approval and permission for the treatment from each country through continuous discussions with each regulatory agency.

Celltrion shares closed up 3.2% on Friday, compared with a 0.3% rise in the wider market.

(Reporting by Joyce Lee; editing by Jason Neely)