EMA plans fast evaluation of Dexamethasone Taw for COVID-19

3 September 2020

The European Medicines Agency has started evaluating an application for the authorization of Dexamethasone Taw for treating hospitalized adult patients with COVID-19.

The application, from UK-based drugmaker Taw Pharma, will be evaluated by the EMA’s human medicines committee, the CHMP, according to an accelerated assessment timetable. This will enable the CHMP to issue an opinion on the benefits and risks of Dexamethasone Taw within the shortest possible timeframe.

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