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  2. Nirmatrelvir/ritonavir - Wikipedia

    en.wikipedia.org/wiki/Nirmatrelvir/ritonavir

    In November 2023, the FDA revised the EUA for nirmatrelvir/ritonavir to authorize EUA- or NDA-labeled nirmatrelvir/ritonavir for the treatment of mild-to-moderate COVID‑19 in people aged twelve years of age and older weighing at least 40 kilograms (88 lb), who are at high risk for progression to severe COVID‑19, including hospitalization. [18]

  3. Treatment and management of COVID-19 - Wikipedia

    en.wikipedia.org/wiki/Treatment_and_management...

    On 16 April 2021, the FDA revoked the emergency use authorization (EUA) for the investigational monoclonal antibody therapy bamlanivimab, when administered alone, to be used for the treatment of mild-to-moderate COVID-19 in adults and certain pediatric patients.

  4. Remdesivir - Wikipedia

    en.wikipedia.org/wiki/Remdesivir

    On 22 October 2020, the FDA approved remdesivir and also revised the EUA to permit the use of remdesivir for treatment of suspected or laboratory confirmed COVID‑19 in hospitalized children weighing 3.5 kilograms (7.7 lb) to less than 40 kilograms (88 lb) or hospitalized children less than twelve years of age weighing at least 3.5 kilograms ...

  5. FDA approves Gilead’s remdesivir as coronavirus treatment - AOL

    www.aol.com/fda-approves-gilead-remdesivir...

    The U.S. Food and Drug Administration has officially approved remdesivir as a treatment for coronavirus, drug manufacturer Gilead Sciences announced Thursday. The Ebola drug was already being used ...

  6. FDA gives emergency authorization to most precise coronavirus ...

    www.aol.com/fda-gives-emergency-authorization...

    The test, which on Wednesday received emergency-use authorization from the U.S. Food and Drug Administration (FDA), measures the number of neutralizing antibodies that the body’s immune system ...

  7. FDA reportedly plans to authorize emergency use of largely ...

    www.aol.com/news/fda-reportedly-plans-authorize...

    The Food and Drug Administration will authorize the emergency use of the antiviral remdesivir on COVID-19 patients as soon as Wednesday, a senior administration official told The New York Times.

  8. Ensitrelvir - Wikipedia

    en.wikipedia.org/wiki/Ensitrelvir

    Shionogi announced they had reached a preliminary agreement to supply 1 million doses to the Japanese government once the drug is approved. The CEO said they could have capacity to make 10 million doses a year. [15] Ensitrelvir may be effective in treating smell and taste loss from COVID-19 infection. In a 2023 study, the drug was associated ...

  9. NEW YORK — A new, next-level coronavirus-antibody test that measures not just antibodies' presence but also how much protection they afford are on the way. The test, which on Wednesday received ...