請更新您的瀏覽器

您使用的瀏覽器版本較舊,已不再受支援。建議您更新瀏覽器版本,以獲得最佳使用體驗。

Eng

EMA conditionally approves Pfizer's COVID-19 pill

XINHUA

發布於 2022年01月27日16:59 • ,

This undated photo shows a Pfizer employee looking at the production of the oral drug Paxlovid. (Pfizer/Handout via Xinhua)

The endorsement allows EU member states to deploy the drug after the EMA gave guidance for its emergency use late last year.

BRUSSELS, Jan. 27 (Xinhua) -- The European Medicines Agency (EMA) on Thursday conditionally approved the use of U.S. multinational biotechnology firm Pfizer's COVID-19 pill for treating adults at risk of severe illness.

The endorsement allows the member states of the European Union (EU) to deploy the drug after the EMA gave guidance for its emergency use late last year.

The EMA said in a statement that its Committee for Medicinal Products for Human Use (CHMP) had "recommended granting a conditional marketing authorization for the oral antiviral medicine Paxlovid for treating COVID-19 in adults who do not require supplemental oxygen and who are at increased risk of the disease becoming severe."

Paxlovid is the first oral antiviral recommended in the EU for treating COVID-19. It consists of two active substances packaged together. One reduces the ability of SARS-CoV-2 to multiply in the body, while the other enables the first substance to remain longer in the body at levels that affect the multiplication of the virus.

This undated photo shows the oral drug Paxlovid made by Pfizer. (Pfizer/Handout via Xinhua)

The EMA said it had evaluated data from a study involving patients with COVID-19, which showed that treatment with Paxlovid significantly reduced the risk of hospitalization and death among patients with at least one underlying condition.

Most patients involved in the study were infected with the Delta variant of coronavirus. Based on laboratory studies, Paxlovid is also expected to be effective against Omicron and other variants, the EMA said, adding that the pill's side effects were mild.

The EMA's recommendation was sent to the European Commission for a rapid decision applicable in all EU member states.

Residents wait to receive AstraZeneca COVID-19 vaccines at a vaccination site in Cornella, Spain, April 7, 2021.  (Photo by Joan Gosa/Xinhua)■

0 0
reaction icon 0
reaction icon 0
reaction icon 0
reaction icon 0
reaction icon 0
reaction icon 0