Copanlisib erzielt objektive Ansprechrate des Tumors von 59% in CHRONOS-1-Studie bei Patienten mit indolentem Non-Hodgkin-Lymphom (iNHL) und zeigt dabei ein gut zu handhabendes Nebenwirkungsprofil
Daten werden in mündlichem Vortrag in einer "Clinical Trials Session" am 4. April beim AACR vorgestellt
Bayer in Gesprächen mit der US-Gesundheitsbehörde FDA bezüglich eines Antrags auf beschleunigte Zulassung ("accelerated approval") für Copanlisib bei follikulärem Lymphom (FL), einer Unterform von iNHL
Copanlisib hat in den USA Fast-Track-Status für FL und Orphan-Drug-Status für FL und Marginalzonenlymphom
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