FDA OKs monoclonal antibody COVID-19 therapy for mild-to-moderate illness
Fox News
The Food and Drug Administration (FDA) on Wednesday granted emergency use authorization to a monoclonal antibody therapy to treat mild-to-moderate COVID-19 in adults and pediatric patients ages 12 and older who are considered at high risk for progression to severe disease.
"With the authorization of this monoclonal antibody treatment, we are providing another option to help keep high-risk patients with COVID-19 out of the hospital," Patrizia Cavazzoni, M.D., director of the FDA’s Center for Drug Evaluation and Research, said. "It is important to expand the arsenal of monoclonal antibody therapies that are expected to retain activity against the circulating variants of COVID-19 in the United States."
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