Pfizer touts antiviral pill results © Getty Images Pfizer announced on Friday that its experimental antiviral COVID-19 pill cut the risk of coronavirus hospitalizations and deaths by 89 percent compared to those who received a placebo, according to an analysis of study data. In a study examining adults who had contracted COVID-19 and were considered at high risk of becoming severely ill, the pharmaceutical company reported that out of 389 people who received the drug, 3 (0.8 percent) were hospitalized, but did not die. The drug is taken as part of a five day regimen —a combination of three pills, taken twice a day— within three days of symptoms beginning. Pfizer said that the study data would be submitted to the Food and Drug Administration (FDA) as soon as possible, which would be included in its emergency use authorization request for the drug. The results were so strong that the independent committee monitoring the trial recommended ending it early. “Today’s news is a real game-changer in the global efforts to halt the devastation of this pandemic. These data suggest that our oral antiviral candidate, if approved or authorized by regulatory authorities, has the potential to save patients’ lives, reduce the severity of COVID-19 infections, and eliminate up to nine out of ten hospitalizations,” Pfizer CEO and Chairman Albert Bourla said in a statement. Significance: Pills that can reduce the severity of a COVID-19 infection could be a game changer in the arsenal of tools helping to manage the pandemic. They aren't meant to replace vaccines, which remain the best way to get protected against severe infection, but could augment them. Drug company Merck has also developed its own antiviral COVID-19 pill, named molnupiravir, which has also been shown to be effective at curbing COVID-19 hospitalizations. An FDA panel is set to examine the evidence for authorization later this month. Read more here. |
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