FDA
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Savara Announces Participation in the 2026 Jefferies Global Healthcare Conference
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Savara Announces the U.K. Medicines and Healthcare Products Regulatory Agency (MHRA) Has Accepted the MOLBREEVI* Marketing Authorisation Application (MAA) for Autoimmune Pulmonary Alveolar Proteinosis
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Savara receives FDA day 74 letter, submits European filing for MOLBREEVI
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Savara Announces Participation in Upcoming Investor Healthcare Conferences
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Savara Resubmits the Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) for MOLBREEVI* for the Potential Treatment of Autoimmune Pulmonary Alveolar Proteinosis (Autoimm
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Savara Reports Third Quarter 2025 Financial Results and Provides Business Update
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Savara Announces Proposed Public Offering
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