FDA prüft Zulassung von Afrezza Inhalationsinsulin für Kinder und Jugendliche

Reuters
Feb 09
FDA prüft Zulassung von Afrezza Inhalationsinsulin für Kinder und Jugendliche

Die US-Arzneimittelbehörde FDA hat im Oktober 2025 die Überprüfung eines ergänzenden Biologics License Application (sBLA) für Afrezza Inhalationspulver bei Kindern und Jugendlichen mit Typ-1- oder Typ-2-Diabetes angenommen. Die MannKind Corporation ist an diesem Verfahren beteiligt. Das voraussichtliche Datum für eine Entscheidung (PDUFA) ist der 29. Mai 2026.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. MannKind Corporation published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 9650708) on February 09, 2026, and is solely responsible for the information contained therein.

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