South Korean drugmaker Celltrion Inc said on Monday it has received regulatory approval for Phase 3 clinical trials of an experimental COVID-19 treatment.
The approval comes as the company plans to seek conditional approval for its antibody-drug, CT-P59, for emergency use by the end of this year.
The treatment, the most advanced antibody-drug in terms of research in South Korea, is directed against the surface of the virus and designed to block it from locking on to human cells.
The third stage trials will be conducted on some 1,000 asymptomatic coronavirus patients and those who have come into close contact with COVID-19 patients in Korea, Celltrion said in a statement.
The Ministry of Food and Drug Safety recently approved a Phase 2/3 study on patients with mild and moderate cases of COVID-19, Lee Sang-joon, Celltrion's senior executive vice president, told Reuters.
Celltrion began commercial production of the drug in September - likely to amount to around 1 million doses - in anticipation of demand in both domestic and overseas markets.
In July, Celltrion separately launched overseas human trials of its treatment in Britain.


Tanzania's Hassan declared landslide winner in election marred by violence
Vietnam's ancient town Hoi An works to restore tourism after devastating floods
Indian temple stampede kills nine, injures several
Turkey to host Gaza meeting amid ceasefire concerns
Tanzania opposition says hundreds killed in vote protests
Turkey sentences 11 people to life in prison over ski resort hotel fire
China sends its youngest astronaut to 'Heavenly Palace' space station
Israel launches more strikes on Gaza overnight, testing fragile truce
