half of the shares offered were already bought by Zambon Pharma: 4.693 M shares that is the the 19.9% of the Savara outstanding shares.
Zanbon is an Italian private Co,with 2800 employees and with sales in Europe , Asia, China, South America but not US, then a perfect commercial partner for the non-US markets. They are also involved in Cystic Fibrosis and respiratory diseases.
IMO a merger could be possible as a medium-term target, likely after Molgradex results and Aerovanc results or interim results.
I hope a merger for a worldwide, multi billions combined company next year.
20% could be a down payment for future agreements.
http://www.zambonpharma.com/en/
http://www.zambonpharma.com/en/therapeutic-areas/rare-diseases/
Zanbon is an Italian private Co,with 2800 employees and with sales in Europe , Asia, China, South America but not US, then a perfect commercial partner for the non-US markets. They are also involved in Cystic Fibrosis and respiratory diseases.
IMO a merger could be possible as a medium-term target, likely after Molgradex results and Aerovanc results or interim results.
I hope a merger for a worldwide, multi billions combined company next year.
20% could be a down payment for future agreements.
http://www.zambonpharma.com/en/
http://www.zambonpharma.com/en/therapeutic-areas/rare-diseases/
Recent SVRA News
- 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 • Business Wire • 05/20/2026 12:15:00 PM
- 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) • Business Wire • 05/19/2026 06:15:00 PM
- 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) • Business Wire • 05/18/2026 06:55:00 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 05/12/2026 08:05:39 PM
- Savara Reports First Quarter Financial Results and Provides Business Update • Business Wire • 05/12/2026 08:05:00 PM
- Savara Announces Participation in the H.C. Wainwright & Co. 4th Annual BioConnect Investor Conference • Business Wire • 05/11/2026 08:05:00 PM
- Form ARS - Annual Report to Security Holders • Edgar (US Regulatory) • 04/24/2026 08:26:53 PM
- Form DEFA14A - Additional definitive proxy soliciting materials and Rule 14(a)(12) material • Edgar (US Regulatory) • 04/24/2026 08:24:46 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 04/24/2026 08:22:42 PM
- Savara Announces New Employment Inducement Grant • Business Wire • 04/17/2026 08:05:00 PM
- 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) • Business Wire • 04/15/2026 08:05:00 PM
- Savara To Present New Data at the American Thoracic Society (ATS) 2026 International Conference • Business Wire • 04/14/2026 12:05:00 PM
- Form PRE 14A - Other preliminary proxy statements • Edgar (US Regulatory) • 04/10/2026 08:18:47 PM
- 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) • Business Wire • 04/07/2026 12:05:00 PM
- Savara Announces European Medicines Agency (EMA) Validation of Marketing Authorization Application (MAA) for MOLBREEVI* in Autoimmune Pulmonary Alveolar Proteinosis (Autoimmune PAP) • Business Wire • 03/30/2026 12:05:00 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/20/2026 08:16:03 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 03/13/2026 12:30:15 PM
- Form 10-K - Annual report [Section 13 and 15(d), not S-K Item 405] • Edgar (US Regulatory) • 03/13/2026 12:10:55 PM
- Savara Reports Fourth Quarter and Year End 2025 Financial Results and Provides Business Update • Business Wire • 03/13/2026 12:05:00 PM
- Savara Provides Regulatory Update on the MOLBREEVI* Development Program in Autoimmune Pulmonary Alveolar Proteinosis (Autoimmune PAP) • Business Wire • 03/06/2026 09:05:00 PM
- Savara Announces Participation in 2026 Citizens Life Sciences Conference • Business Wire • 03/04/2026 09:05:00 PM
- Savara Announces the U.S. Food and Drug Administration (FDA) Filed the MOLBREEVI* Biologics License Application (BLA) in Autoimmune Pulmonary Alveolar Proteinosis (Autoimmune PAP) • Business Wire • 02/20/2026 09:15:00 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 02/17/2026 10:30:13 PM
