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FDA to authorize emergency use of new coronavirus treatment

The Trump administration is fast-tracking authorization of the drug remdesivir as a treatment for COVID-19.

The Food and Drug Administration (FDA) on Friday announced the drug will receive an “emergency use authorization” after it showed promising results during a clinical trial.

Early results released this week showed the drug had modest success in reducing the time COVID-19 patients were in the hospital. Continue reading.

Data and Research Manager: