Savara (SVRA) Proxy filing summary
Event summary combining transcript, slides, and related documents.
Proxy filing summary
24 Apr, 2026Executive summary
Annual meeting scheduled for June 4, 2026, to be held virtually, with key proposals including director elections, amendments to the certificate of incorporation and incentive plan, auditor ratification, and a say-on-pay vote.
Company is preparing for potential commercial launch of molgramostim inhalation solution (MOLBREEVI) for autoimmune PAP, with regulatory reviews ongoing in the U.S., EU, and UK.
Recent financial actions include $149.5 million equity financing, a $75 million royalty funding agreement, and an amended debt facility for up to $75 million upon FDA approval.
Voting matters and shareholder proposals
Six directors nominated for election to serve until the next annual meeting.
Proposal to amend the certificate of incorporation to increase authorized common stock from 300 million to 600 million shares.
Proposal to amend the 2024 Omnibus Incentive Plan to add 18.9 million shares for issuance.
Ratification of RSM US LLP as independent auditor for fiscal year 2026.
Advisory vote on executive compensation (say-on-pay).
Board of directors and corporate governance
Board consists of six members with diverse expertise in pharmaceuticals, finance, and governance.
All directors except the CEO are independent under Nasdaq standards.
Board committees: Audit, Compensation, and Nominating & Governance, all comprised of independent directors.
Lead Independent Director role established; board meets at least quarterly, with independent sessions annually.
Director resignation policy in place for those not re-elected.
Prohibition on hedging and speculative transactions for directors and employees.
Latest events from Savara
- Key votes include director elections, share authorization increase, and auditor ratification.SVRA
Proxy filing24 Apr 2026 - MOLBREEVI nears FDA priority review, targeting August approval and rapid rare disease market entry.SVRA
Guggenheim Securities Emerging Outlook: Biotech Summit 202611 Apr 2026 - Key votes on board, capital, incentives, and auditor as company prepares for product launch.SVRA
Proxy filing10 Apr 2026 - MOLBREEVI shows strong efficacy and safety for autoimmune PAP, targeting a $2B+ U.S. market.SVRA
Corporate presentation7 Apr 2026 - MOLBREEVI demonstrated strong efficacy and safety in autoimmune PAP, targeting a $2B+ U.S. market.SVRA
Corporate presentation30 Mar 2026 - Regulatory progress and robust cash position set the stage for a potential 2026 launch.SVRA
Q4 202513 Mar 2026 - MOLBREEVI demonstrated strong efficacy and safety in autoimmune PAP, targeting a $2B+ U.S. market.SVRA
Corporate presentation13 Mar 2026 - MOLBREEVI nears FDA approval for autoimmune PAP, with launch prep and strong clinical data.SVRA
The Citizens Life Sciences Conference 202611 Mar 2026 - MOLBREEVI demonstrated significant efficacy and safety in autoimmune PAP, targeting a $2B+ U.S. market.SVRA
Corporate presentation11 Mar 2026