Highlights

05-18 Savara Inc Announces New Exercise Capacity Data From The IMPALA-2 Phase 3 Clinical Trial Of Molgramostim Inhalation Solution In Autoimmune Pulmonary Alveolar Proteinosis CI
05-12 Savara Q1 Loss Widens MT
05-12 Earnings Flash (SVRA) Savara Posts Q1 Per Share Loss $-0.15, vs. FactSet Est of $-0.13 Loss MT
05-12 Savara Inc. Reports Earnings Results for the First Quarter Ended March 31, 2026 CI
04-15 Savara Announces the U.S. Food & Drug Administration Has Extended the Review Period for the Molgramostim Inhalation Solution (Molgramostim) Biologics License Application in Autoimmune Pulmonary Alveolar Proteinosis CI
04-07 Savara Inc. Announces MHRA Accepts Molbreevi Marketing Authorisation Application for Autoimmune PAP CI
04-07 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 (autoimmune PAP) RE
03-30 Savara Says EMA Validates Marketing Authorization Application for Molbreevi to Treat Lung Disease MT
03-30 Savara Inc. Announces Validation Of Marketing Authorization Application For Molbreevi In Autoimmune Pulmonary Alveolar Proteinosis CI
03-13 Savara Inc. Reports Earnings Results for the Fourth Quarter Ended December 31, 2025 CI
03-13 Savara Q4 Loss Unchanged From Year Earlier MT
03-13 Savara Inc Enters into Agreement of Lease for New Headquarters CI
03-13 Earnings Flash (SVRA) Savara Posts Q4 Loss $0.13 a Share, vs. FactSet Est of $0.12 Loss MT
03-06 Savara Says FDA Letter Indicates No Advisory Committee Meeting Planned for Molbreevi Application MT
03-06 Savara Inc Provides Regulatory Update on the Molbreevi Development Program in Autoimmune Pulmonary Alveolar Proteinosis CI
02-20 Savara Inc. Announces U.S. Food and Drug Administration Filed the MOLBREEVI Biologics License Application in Autoimmune Pulmonary Alveolar Proteinosis (Autoimmune PAP) CI
01-08 Savara Inc. Announces an Exclusive Distribution Agreement for MOLBREEVI CI
12-22 Savara resubmits the Biologics License Application to the U.S. Food and Drug Administration for Molbreevi RE
12-22 Savara Inc. Resubmits the Biologics License Application to the U.S. Food and Drug Administration for Molbreevi for the Potential Treatment of Autoimmune Pulmonary Alveolar Proteinosis CI
12-11 Savara Inc. Announces European Patent Office Intends to Grant A Patent for the Liquid Formulation of MOLBREEVI CI
12-02 Savara, PARI Granted European Patent Covering Drug-Device Combination MT
11-12 Savara Q3 net loss widens  RE
11-12 Savara Inc. Reports Earnings Results for the Third Quarter and Nine Months Ended September 30, 2025 CI
31/10/25 Savara Closes $149.5 Million Public Offering MT
30/10/25 Savara announces pricing of public offering at $4.20 per share RE
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