Trump administration officials fought over whether — and ultimately declined — to fund the same antiviral drug that Merck announced yesterday significantly reduces hospitalizations and deaths among coronavirus patients.
Trump administration officials fought over whether — and ultimately declined — to fund the same antiviral drug that Merck announced yesterdayThe Trump administration's decision almost certainly delayed the development of the drug. Having an effective antiviral pill during the Delta wave could have substantially reduced its death toll.
The drug "was presented as a 'miracle cure' for influenza, Ebola and nearly every other virus, even though the developer had not yet conducted clinical trials and no data had been compiled to demonstrate either the efficacy or safety of the drug in humans," Bright wrote. But another top health official, Robert Kadlec, had "indicated his enthusiasm for [the drug]’s potential."
BARDA ultimately declined to fund the manufacturing of the drug — which had already received $30 million from the federal government for phase 1 clinical trials — until more data was available. In late February of last year, the Emory researcher and Ridgeback Biotherapeutics asked for federal funding of the drug again, but as a treatment for COVID-19. Officials fought again, and ultimately declined to fund the drug.
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Merck Pill Intended to Be Covid-19’s Tamiflu Succeeds in Key StudyMerck said its experimental pill helped prevent serious illness and death in high-risk people infected with Covid-19, a step toward the virus’s first at-home treatment
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Merck COVID-19 pill success slams Moderna shares, shakes up healthcare sectorPositive clinical trial results for Merck & Co's experimental antiviral COVID-19 pill reverberated through the healthcare sector on Friday, sending the drugmaker's stock price soaring while denting high-flying shares of vaccine companies and makers of other coronavirus therapies.
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Merck says its new Covid pill reduces the risk of hospitalization, death by half for some patientsMerck and Ridgeback Biotherapeutics will seek emergency authorization for their drug, which they say could have “a profound impact in controlling the pandemic.”
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