Eli Lilly Seeks Approval for Experimental COVID-19 Antibody Drug
2020-10-08
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1Drug maker Eli Lilly and Company said Wednesday it has asked U.S. officials to approve emergency use of an experimental antibody treatment for COVID-19.
2Lilly said early results of a study show the treatment reduced hospital emergency room visits for persons with mild or moderate forms of COVID-19.
3It said the therapy also reduced signs of the disease, the amount of the virus and length of hospital stays for such patients.
4The company announced the study's partial results before a meeting with investors and the public.
5The findings have yet to be published or examined by independent scientists.
6The antibody treatment appears to work like one given to President Donald Trump last Friday.
7The treatment he took was developed by Regeneron Pharmaceuticals.
8Both therapies are designed to connect human antibodies to the coronavirus that causes COVID-19 and limit its ability to spread.
9The antibodies are usually given as a one-time treatment through intravenous therapy.
10Daniel Skovronsky is a doctor and Eli Lilly's chief scientific officer.
11He said in a statement, "We believe the data generated to date provide sufficient evidence that both monotherapy and combination therapy may be effective to treat COVID-19 in patients with a high risk for serious outcomes."
12The monotherapy involves an antibody called LY-CoV555.
13The combination therapy combines that antibody with an antibody called LY-CoV016.
14The medical news website StatNews reported that "Lilly had previously released results for a similar treatment using one antibody, which experts viewed as promising.
15But the new results, of a combination of two antibodies, appear, based on limited data provided in a press release, to be more robust."
16The drug maker is asking the U.S. Food and Drug Administration (FDA) to permit use of its single antibody treatment in emergency situations.
17The company expects to seek government approval of the combination treatment in November.
18At this time, the FDA has only approved the drug remdesivir for emergency use in COVID-19 patients.
19The president's personal doctor confirmed that Trump has also started a five-day treatment of remdesivir.
20Lilly said it has already started manufacturing the drug LY-CoV555.
21The company expects to have 100,000 doses ready in October and 1 million by the end of the year.
22It hopes to have 50,000 doses of the combination therapy ready by year's end.
23The drug maker added that it is also "working with regulators around the world to make these treatments available."
24I'm Jonathan Evans.
1Drug maker Eli Lilly and Company said Wednesday it has asked U.S. officials to approve emergency use of an experimental antibody treatment for COVID-19. 2Lilly said early results of a study show the treatment reduced hospital emergency room visits for persons with mild or moderate forms of COVID-19. It said the therapy also reduced signs of the disease, the amount of the virus and length of hospital stays for such patients. 3The company announced the study's partial results before a meeting with investors and the public. The findings have yet to be published or examined by independent scientists. 4The antibody treatment appears to work like one given to President Donald Trump last Friday. The treatment he took was developed by Regeneron Pharmaceuticals. 5Both therapies are designed to connect human antibodies to the coronavirus that causes COVID-19 and limit its ability to spread. The antibodies are usually given as a one-time treatment through intravenous therapy. 6Daniel Skovronsky is a doctor and Eli Lilly's chief scientific officer. He said in a statement, "We believe the data generated to date provide sufficient evidence that both monotherapy and combination therapy may be effective to treat COVID-19 in patients with a high risk for serious outcomes." 7The monotherapy involves an antibody called LY-CoV555. The combination therapy combines that antibody with an antibody called LY-CoV016. 8The medical news website StatNews reported that "Lilly had previously released results for a similar treatment using one antibody, which experts viewed as promising. But the new results, of a combination of two antibodies, appear, based on limited data provided in a press release, to be more robust." 9The drug maker is asking the U.S. Food and Drug Administration (FDA) to permit use of its single antibody treatment in emergency situations. The company expects to seek government approval of the combination treatment in November. 10At this time, the FDA has only approved the drug remdesivir for emergency use in COVID-19 patients. The president's personal doctor confirmed that Trump has also started a five-day treatment of remdesivir. 11Lilly said it has already started manufacturing the drug LY-CoV555. The company expects to have 100,000 doses ready in October and 1 million by the end of the year. It hopes to have 50,000 doses of the combination therapy ready by year's end. 12The drug maker added that it is also "working with regulators around the world to make these treatments available." 13I'm Jonathan Evans. 14Hai Do wrote this story for Learning English. George Grow was the editor. 15________________________________________________________________ 16Words in This Story 17intravenous - adj. through a vein 18monotherapy - n. the use of a single drug to treat a disease or condition 19outcome - n. something that happens as a result of an activity or process 20view - v. to think about something in a particular way 21robust - adj. strongly formed 22dose - n. the amount of medicine 23regulator - n. a government official who controls the public activity by making and enforcing rules