Pill lowers risk of hospitalization, death: study © Pfizer Media Relations via AP Pfizer announced Tuesday that a study found that its oral, antiviral COVID-19 pill Paxlovid reduced the risk of hospitalization or death by 89 percent in high-risk patients. Pfizer said that the 2,246 patients in the study were given the pill within three days of symptom onset, adding that they had mild to moderate symptoms as well as an underlying medical condition or an increased risk of becoming severely infected by COVID-19. The company said the results have been shared with the Food and Drug Administration (FDA) as a part of the company's request for emergency use authorization. Pfizer requested emergency use authorization from the FDA for Paxlovid in mid-November. Takeaway: Health officials stress the pill is not a substitute for the vaccine, but it does have the potential to significantly cut down on hospitalizations and deaths, assuming people start taking the pill within three days of their symptoms starting. Pfizer added that it believes that the pill will work on the new omicron variant, but additional studies are underway. “This news provides further corroboration that our oral antiviral candidate, if authorized or approved, could have a meaningful impact on the lives of many," said Albert Bourla, Pfizer's chairman and chief executive officer. “Emerging variants of concern, like Omicron, have exacerbated the need for accessible treatment options for those who contract the virus, and we are confident that, if authorized or approved, this potential treatment could be a critical tool to help quell the pandemic.” Supply is expected to be extremely limited at first. The company is expected to deliver only enough of its pills to cover 300,000 Americans before the end of February. Read more here. |
No comments:
Post a Comment