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S. Korea expects 3 more homegrown COVID-19 treatments in H1

Yonhap Korea Stories 12:00 February 13, 2021

By Kim Han-joo

SEOUL, Feb. 13 (Yonhap) -- Three homegrown treatments for the novel coronavirus are expected to receive approval as early as the first half of this year as the country speeds up the approval process amid the pandemic.

Last week, the country's drug safety agency approved pharmaceutical giant Celltrion Inc.'s CT-P59, an anti-COVID-19 monoclonal antibody treatment, marking the country's first homegrown treatment.

This photo, provided by South Korea drug firm Chong Kun Dang Pharmaceutical Corp. on Dec. 14, 2020, shows Nafabeltan, which is currently used as a blood anticoagulant and acute pancreatitis treatment. (PHOTO NOT FOR SALE) (Yonhap)

The treatment will be provided to medical institutions starting in mid-February. It can only be administered to patients who have received approval from the drug ministry. They will most likely be elderly patients aged over 60 or those with chronic illnesses.

Another three leading players -- Chong Kun Dang Pharmaceutical Corp., GC Pharma, and Daewoong Pharmaceutical Co. -- have joined the race to launch the country's second homegrown COVID-19 treatment.

Among the front runners are the acute pancreatitis drug Nafabeltan by Chong Kun Dang.

The firm is expected to seek conditional approval from the Ministry of Food and Drug Safety within this month, following the successful conclusion of its second phase clinical trial in Russia.

Chong Kun Dang said Nafabeltan -- currently used as a blood anticoagulant and acute pancreatitis treatment -- showed the most potent antiviral efficacy against the COVID-19 virus when it is administered to COVID-19 patients with severe symptoms of pneumonia.

This undated photo, provided by South Korean biotech company GC Pharma, shows a company official at its plant. (PHOTO NOT FOR SALE) (Yonhap)

GC Pharma also completed a phase two clinical trial of its plasma therapy treatment, known as GC5131A, in the local market.

The drug is a type of hyperimmune globulin drug that uses blood plasma taken from people who have fully recovered from COVID-19.

The company said it plans to file for a conditional approval in April after announcing the result of its clinical study in March.

GC Pharma said it has already completed the production of its third batch, meaning the treatment candidate is expected to be available at medical institutions immediately.

People who have recovered from COVID-19 develop natural defenses against the disease in their blood, in which antibodies are found in the part of the blood called plasma.

Daewoong Pharmaceutical is also planning to conduct a phase three clinical trial of its drug to treat the novel coronavirus. The company was unable to achieve meaningful data from its second phase clinical study.

Foistar, an oral protease inhibitor, will be administered to 1,012 COVID-19 patients at two hospitals in Seoul starting later this month, the company said. The drug, also known as Camostat, was approved in the country in 2012 as a therapeutic agent for chronic pancreatitis.

This undated photo, provided by South Korean drugmaker Daewoong Pharmaceutical Co., shows the company's headquarters. (PHOTO NOT FOR SALE) (Yonhap)

khj@Yna.co.kr
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