Zeit für Hoffnung? Die Europäische Arzneimittel-Agentur (EMA) plant kurzfristig eine bedingte Marktzulassung für die Behandlung von Covid-19-Patienten mit Remdesivir. Das bestätigte gestern EMA-Sprecherin Sophie Labbe auf Nachfrage von Tagesspiegel Background. Diese könnte bereits in den kommenden Tagen erteilt werden, hieß es aus Brüssel. Doch die Meinungen und Urteile gehen stark auseinander, wie viel Hoffnung tatsächlich geboten ist.
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