Logotype for Vaxart Inc

Vaxart (VXRT) Q2 2026 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Vaxart Inc

Q2 2026 earnings summary

12 Aug, 2026

Executive summary

  • Achieved positive 12-month safety data from the Phase 2b COVID-19 oral pill vaccine sentinel cohort, showing no vaccine-related serious adverse events and a favorable safety profile compared to mRNA comparators, validating the oral vaccine platform and supporting further clinical progress.

  • Finalized a BARDA contract modification, unlocking dedicated funding for deeper scientific analysis and expanded trial analytics, with total authorized study funding now at $344.8 million.

  • Collaboration with Dynavax (now part of Sanofi) for the COVID-19 oral vaccine continues, with potential milestone payments pending trial outcomes.

  • Enhanced corporate governance through board reorganization, new committee formation, and a cooperation agreement with a shareholder group.

  • Focused on oral recombinant vaccines for infectious diseases, with lead programs in norovirus and COVID-19, and early-stage HPV and influenza candidates.

Financial highlights

  • Q2 2026 revenue was $27.2 million, down 32% year-over-year from $39.7 million, primarily from BARDA contracts and $2.9 million from a Dynavax agreement; six-month revenue was $66.4 million, up 10%.

  • Research and development expenses decreased to $33.7 million from $49.7 million year-over-year, while general and administrative expenses increased to $6.6 million from $4.6 million.

  • Net loss for Q2 2026 was $13.5 million ($0.06/share), improved from $15 million ($0.07/share) in Q2 2025; six-month net loss was $8.3 million, a 73% improvement year-over-year.

  • Cash, cash equivalents, and short-term investments totaled $64.0 million as of June 30, 2026, with a projected runway into Q2 2027.

  • Maintains a $25 million share purchase agreement with Lincoln Park Capital for flexible capital access, with minimal drawdown to date.

Outlook and guidance

  • Topline efficacy and safety data from the full ~5,400 participant Phase 2b COVID-19 trial cohort expected in the first half of 2027.

  • Actively seeking non-dilutive funding and strategic partnerships to extend cash runway and support pipeline advancement; management may reduce or delay expenses if unable to raise further capital.

  • Norovirus program advancement contingent on securing partnership or non-dilutive funding; timeline not disclosed due to funding uncertainty.

Partial view of Summaries dataset, powered by Quartr API
AI can get things wrong. Verify important information.
All investor relations material. One API.
Learn more