Savara Inc. announced that the European Patent Office has notified the company of its intention to grant a patent application covering the liquid formulation of MOLBREEVI, an orally inhaled recombinant human GM-CSF for the treatment of autoimmune pulmonary alveolar proteinosis (PAP). The liquid formulation and drug-device patents are expected to provide protection in Europe through March 2041 and March 2043, respectively. MOLBREEVI has also received multiple regulatory designations, including Orphan Drug status in both the U.S. and Europe.
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: 20251211393845) on December 11, 2025, and is solely responsible for the information contained therein.
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