Außerdem erhielt das Unternehmen heute von der US-amerikanischen Zulassungsbehörde FDA einen sogenannten "Not Approvable Letter", d.h. zunächst eine Ablehnung seines Zulassungsantrages für Icatibant in der Indikation HAE. Jerini prüft derzeit den Inhalt des Schreibens und plant, die in dem Schreiben aufgeführten Bedenken der Behörde dl rrracyq kko qdnyatg oah wyu FXN cy jiaknskh.
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