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from: Kaohsiung
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| 2021-11-05 04:20:33 | onclick： | Britain took the lead in approving the use of Merck oral anti neocrown drugs |
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The British drug and health products administration announced on the 4th that it has approved the oral anti new crown drug monabilavir developed by Merck in the United States for specific new crown patients. This is the world's first anti Xinguan oral drug.
The British drug and health products administration said in a communique 4 days that the head of the new crown has been approved for mild to moderate symptoms. These patients have at least one risk factor for worsening of the disease, including obesity, over 60 years of age, diabetes and heart disease.
It is a small molecule broad-spectrum antiviral oral drug directed against RNA virus, which is developed by Merck Co and Rich Barker biopharmaceutical company of the United States. It inhibits COVID-19 replication. According to the interim analysis data of phase III clinical trial released by Merck in early October, the drug can reduce the risk of hospitalization or death of patients with mild to moderate symptoms by about 50%.
The communique said that the human drugs Committee, an independent expert advisory group of British regulators and the government, has strictly reviewed its safety, quality and effectiveness, making it the first oral antiviral drug approved for the treatment of new crown infection. The communique quoted British health secretary said Javed as saying that for the most vulnerable and immunosuppressed patients, approving the drug will "change the rules of the game", and these people will soon be able to receive breakthrough treatment.
The UK is the first country in the world to officially approve the use of monabilavir in the treatment of patients with new crowns. The European Drug Administration said on October 5 that it would consider starting the rapid approval of monabilavir. Merck submitted an application for emergency use authorization of the drug to the U.S. Food and Drug Administration in October.
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