FDA accepts Savara’s MOLBREEVI BLA for priority review in autoimmune PAP

Reuters

02/21

Savara Inc. said the U.S. Food and Drug Administration has filed for review its Biologics License Application for MOLBREEVI to treat autoimmune pulmonary alveolar proteinosis. The FDA granted Priority Review and set a PDUFA action date of August 22, 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. Savara Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20260220017435) on February 20, 2026, and is solely responsible for the information contained therein.

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The FDA granted Priority Review and set a PDUFA action date of August 22, 2026.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<p>\n<i>Disclaimer: <span>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. Savara Inc. published the original content used to generate this news brief via Business Wire (Ref. 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