Zevra Therapeutics (ZVRA) Proxy filing summary
Event summary combining transcript, slides, and related documents.
Proxy filing summary
6 Apr, 2026Executive summary
Achieved $106.5M in net revenue for 2025, with $87.4M from MIPLYFFA, reaching over 40% of diagnosed NPC patients in the U.S. in its first full year of commercialization.
Advanced global pipeline, including EU Marketing Authorization Application for arimoclomol and progress in Phase 3 DISCOVER trial of celiprolol.
Strengthened financial position by selling a Rare Pediatric Disease Priority Review Voucher for $150M and fully repaying term loan.
Enhanced leadership with new CFO and Board member appointments, and relocated headquarters to Boston for better access to biotech talent.
Voting matters and shareholder proposals
Election of two Class II directors (Douglas W. Calder and Corey Watton) to serve until the 2029 annual meeting.
Ratification of Ernst & Young LLP as independent registered public accounting firm for fiscal year ending December 31, 2026.
Approval of amendment to phase out classified Board structure, moving to annual election of all directors starting in 2027.
Board of directors and corporate governance
Board consists of eight members, 87.5% independent, with diverse skills in leadership, finance, and industry.
Board Chair and CEO roles are separated to reinforce independence; Board regularly reviews governance practices and composition.
Board committees (Audit, Compensation, Nominating & Corporate Governance) are 100% independent.
Board conducts annual performance reviews and succession planning.
If declassification is approved, Board will transition to annual elections by 2029.
Latest events from Zevra Therapeutics
- MIPLYFFA drives growth as a foundational NPC therapy, fueling expansion and pipeline innovation.ZVRA
Corporate presentation16 Mar 2026 - MIPLYFFA drives rare disease growth with strong revenue, global expansion, and pipeline progress.ZVRA
The Citizens Life Sciences Conference 202611 Mar 2026 - FY 2025 net income was $83.2M on $106.5M revenue, driven by MIPLYFFA's strong growth.ZVRA
Q4 20259 Mar 2026 - Strong rare disease portfolio, rapid product uptake, and robust financial position drive growth.ZVRA
TD Cowen 45th Annual Healthcare Conference3 Feb 2026 - Arimoclomol set for U.S. launch, with global expansion and robust pipeline development underway.ZVRA
Canaccord Genuity 44th Annual Growth Conference & Private Company Showcase 20242 Feb 2026 - Favorable FDA vote, OLPRUVA progress, and $64.5M offering extend cash runway into 2027.ZVRA
Q2 20241 Feb 2026 - Strong physician interest, market synergy, and pipeline progress drive optimism for upcoming approvals.ZVRA
H.C. Wainwright 26th Annual Global Investment Conference 202421 Jan 2026 - Preparing for arimoclomol launch, expanding rare disease reach, and advancing a strong pipeline.ZVRA
2024 Cantor Fitzgerald Global Healthcare Conference20 Jan 2026 - FDA approved MIPLYFFA for NPC, halting disease progression and enabling broad patient access.ZVRA
FDA Announcement20 Jan 2026