No Fast Route To EU Market For Dova's Avatrombopag
Dova’s avatrombopag, which was recently approved in the US under priority review, has been refused an accelerated assessment in the EU.
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Fourteen new products have been added to the European Medicines Agency’s list of medicines under review for marketing authorization across the EU.
There has been a sharp fall in the number of companies seeking accelerated assessment for their investigational products at the European Medicines Agency. One such company that has asked – Dova Pharmaceuticals – is staying silent on the outcome of its request.