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Savara, Inc. (NASDAQ:SVRA) news

Savara, Inc. news releases on 6ix. Latest, Aug 25, 2026: Savara Announces Encore Presentations of Results from the Phase 3 Clinical Trial of Molgramostim…

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Press releases & updates

Savara Announces Encore Presentations of Results from the Phase 3 Clinical Trial of Molgramostim Inhalation Solution (Molgramostim) in Autoimmune Pulmonary Alveolar Proteinosis (APAP)

August 25, 2026

Savara Announces Encore Presentations of Results from the Phase 3 Clinical Trial of Molgramostim Inhalation Solution (Molgramostim) in Autoimmune Pulmonary Alveolar Proteinosis (APAP) at the European Respiratory Society (ERS) Congress 2026

August 24, 2026

Savara Reports Second Quarter 2026 Financial Results and Provides Business Update

August 11, 2026

Savara Announces European and Australian Patent Offices Have Granted Patents for the Liquid Formulation of MOLBREEVI*, Providing Protection in Europe and Australia Until March 2041

July 30, 2026

Savara Announces Chief Financial and Administrative Officer Transition

June 8, 2026

Savara Announces Participation in the 2026 Jefferies Global Healthcare Conference

May 27, 2026

Savara Presented New Biomarker Data from the IMPALA-2 Phase 3 Clinical Trial of Molgramostim Inhalation Solution (Molgramostim) in Autoimmune Pulmonary Alveolar Proteinosis (aPAP) at the American Thoracic Society (ATS) International Conference 2026

May 20, 2026

Savara Presented Long-Term Efficacy and Safety Data from the Ongoing IMPALA-2 Phase 3 Clinical Trial Open-Label (OL) Extension of Molgramostim Inhalation Solution (Molgramostim) in Autoimmune Pulmonary Alveolar Proteinosis (aPAP)

May 19, 2026

Savara Announces New Exercise Capacity Data from the IMPALA-2 Phase 3 Clinical Trial of Molgramostim Inhalation Solution (Molgramostim) in Autoimmune Pulmonary Alveolar Proteinosis (aPAP)

May 18, 2026

Savara Announces Participation in the H.C. Wainwright & Co. 4th Annual BioConnect Investor Conference

May 11, 2026

Savara Announces the U.S. Food & Drug Administration (FDA) Has Extended the Review Period for the Molgramostim Inhalation Solution (Molgramostim) Biologics License Application (BLA) in Autoimmune Pulmonary Alveolar Proteinosis (Autoimmune PAP)

April 14, 2026

Savara To Present New Data at the American Thoracic Society (ATS) 2026 International Conference

April 14, 2026

Savara Announces the U.K. Medicines and Healthcare Products Regulatory Agency Has Accepted the MOLBREEVI Marketing Authorisation Application for Autoimmune Pulmonary Alveolar Proteinosis

April 8, 2026

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)

April 6, 2026

Savara Announces European Medicines Agency (EMA) Validation of Marketing Authorization Application (MAA) for MOLBREEVI* in Autoimmune Pulmonary Alveolar Proteinosis (Autoimmune PAP)

March 29, 2026

Savara Reports Fourth Quarter and Year End 2025 Financial Results and Provides Business Update

March 13, 2026

Savara Provides Regulatory Update on the MOLBREEVI Development Program in Autoimmune Pulmonary Alveolar Proteinosis

March 9, 2026

Savara Provides Regulatory Update on the MOLBREEVI* Development Program in Autoimmune Pulmonary Alveolar Proteinosis (Autoimmune PAP)

March 5, 2026

Savara Announces Participation in 2026 Citizens Life Sciences Conference

March 3, 2026

Savara Announces the U.S. Food and Drug Administration (FDA) Filed the MOLBREEVI* Biologics License Application (BLA) in Autoimmune Pulmonary Alveolar Proteinosis (Autoimmune PAP)

February 20, 2026

Savara Announces Amendment to Hercules Capital Debt Facility Providing up to $75M of Additional Debt Funding Upon U.S. Food and Drug Administration (FDA) Approval of MOLBREEVI*

January 26, 2026

Savara Announces New Employment Inducement Grant

January 16, 2026

PANTHERx® Rare Selected by Savara as the U.S. Exclusive Specialty Pharmacy for MOLBREEVI*

January 8, 2026

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 (Autoimmune PAP)

December 21, 2025

Savara Announces Participation in the 44th Annual J.P. Morgan Healthcare Conference

December 16, 2025

Savara Announces European Patent Office (EPO) Intends to Grant a Patent for the Liquid Formulation of MOLBREEVI*

December 10, 2025

Savara and PARI Granted a European Patent Covering the Drug-Device Combination of MOLBREEVI* Delivered Via the Proprietary eFlow® Nebulizer System

December 1, 2025

Savara Announces Participation in Upcoming Investor Healthcare Conferences

November 19, 2025

Savara Reports Third Quarter 2025 Financial Results and Provides Business Update

November 11, 2025

Savara Announces Closing of Public Offering and Full Exercise of the Underwriters’ Option to Purchase Additional Shares for Total Gross Proceeds of $149.5M

October 30, 2025

Savara Announces Proposed Public Offering

October 28, 2025

Savara Announces Pricing of $130.0 Million Public Offering of Common Stock and Pre-funded Warrants

October 28, 2025

Savara announces $75M Royalty Funding Agreement with RTW to Support the Potential Launch of MOLBREEVI* in Autoimmune Pulmonary Alveolar Proteinosis (Autoimmune PAP)

October 28, 2025

Savara Announces Chief Medical Officer (CMO) Transition

October 16, 2025

Savara Announces Encore Presentations of Results From the Phase 3 IMPALA-2 Clinical Trial of Molgramostim Inhalation Solution (Molgramostim) in Patients with Autoimmune Pulmonary Alveolar Proteinosis (aPAP) at CHEST 2025

October 1, 2025

Savara Presents New Data From the Phase 3 IMPALA-2 Clinical Trial of Molgramostim Inhalation Solution (Molgramostim) in Patients With Autoimmune Pulmonary Alveolar Proteinosis (aPAP) at the European Respiratory Society (ERS) Congress 2025

September 28, 2025

Savara Announces New U.S. Health Claims Data Analysis Finds Over 50% Increase in the Estimated Number of Autoimmune Pulmonary Alveolar Proteinosis (Autoimmune PAP) Patients Compared to Previous Claims Analysis

September 1, 2025

New England Journal of Medicine (NEJM) to Publish Results From Savara’s Pivotal Phase 3 IMPALA-2 Clinical Trial in Autoimmune Pulmonary Alveolar Proteinosis (Autoimmune PAP)

August 19, 2025

Savara to Present New Data from the Phase 3 IMPALA-2 Trial of Molgramostim Inhalation Solution (Molgramostim) in Patients with Autoimmune Pulmonary Alveolar Proteinosis (aPAP) at the European Respiratory Society Congress 2025

August 17, 2025

Savara Reports Second Quarter 2025 Financial Results and Provides a Business Update

August 12, 2025

Savara Receives Refusal to File (RTF) Letter From the U.S. Food and Drug Administration (FDA) for the Biologics License Application (BLA) for MOLBREEVI* to Treat Patients With Autoimmune Pulmonary Alveolar Proteinosis (autoimmune PAP)

May 26, 2025

Savara Announces Participation in Jefferies Global Healthcare Conference

May 21, 2025

Savara Presented New Data From Pivotal Phase 3 IMPALA-2 Trial of Molgramostim Inhalation Solution (Molgramostim) in Patients With Autoimmune Pulmonary Alveolar Proteinosis (aPAP) at American Thoracic Society Conference (ATS) 2025

May 17, 2025

Savara Reports First Quarter 2025 Financial Results and Provides a Business Update

May 12, 2025

Savara Announces Participation in the H.C. Wainwright & Co. 3rd Annual BioConnect Investor Conference

May 11, 2025

Savara Announces Participation in the Upcoming Citizens Life Sciences Conference

May 1, 2025

Savara Announces Participation in the Upcoming Citizens Life Sciences Conference

April 30, 2025

Savara Announces Encore Presentations From the Phase 3 IMPALA-2 Trial of Molgramostim Inhalation Solution (Molgramostim) in Patients With Autoimmune Pulmonary Alveolar Proteinosis (aPAP) at Two Upcoming Scientific Conferences

April 6, 2025

Savara Reports Fourth Quarter and Year End 2024 Financial Results and Provides Business Update

March 26, 2025

Savara Enters Into Non-Dilutive Debt Financing for up to $200M With Hercules Capital

March 25, 2025

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