VXRT
NASDAQ · Healthcare · Biotechnology · US
Next report
Analyst consensus
- Next report date
- Nov 12, 2026
- EPS estimate
- -$0.31
- Revenue estimate
- $14.6M
Latest reported
- Last report date
- Aug 7, 2026
- EPS actual
- -$0.06
- EPS estimate
- -$0.12
- Revenue actual
- $27.2M
- Revenue estimate
- $26.2M
Track record
Trailing twelve quarters
- EPS beats (12Q)
- 9
- EPS misses (12Q)
- 1
- EPS in line (12Q)
- 2
- Avg surprise (4Q)
- +122.9%
- Revenue beats (12Q)
- 6
Q1 FY2026 · May 8, 2026
AI summary of management’s prepared remarks and analyst Q&A · For informational purposes only, not investment advice
Management highlights
• Progressed clinical programs and prepared for key data milestones, including COVID-19 program's Sentinel cohort data disclosure. • Strengthened financial position by establishing $25 million share purchase agreement and moving headquarters. • Added Dr. James Breitmaier to board for clinical and strategic oversight. • Continues dialogue with Sanofi on COVID-19 program. • Evaluating norovirus second-generation constructs and refining platform and manufacturing processes.
Guidance
• Anticipates primary efficacy and safety data readout from ~5,000 participant main COVID-19 study cohort in early 2027. • Norovirus next clinical trial planned for 2026 depending on partnership or funding. • Cash runway expected to extend into second quarter of 2027.
Segment performance
VaxArt ended the first quarter with cash, cash equivalents, and short-term investments of $61 million. Revenue for the first quarter was $39.2 million compared to $20.9 million last year, with growth driven by BARDA contract and Dynamax license and collaboration agreement. R&D and G&A expenses were reduced. The 400-person Sentinel cohort of Phase IIb COVID-19 trial is in data validation stage. Norovirus program is in preclinical stage with plan to initiate next clinical trial in 2026.
Risks & headwinds
• Uncertainty in clinical development and regulatory process. • Risks described in Form 10-K and other public periodic reports filed with SEC. • Procedural steps with BARDA for data disclosure taking longer than anticipated could impact timeline.
Analyst Q&A
Q: Primary focus of Sentinel readout and timeline for release.
A: Sentinel cohort for safety and immunogenicity, not definitive efficacy. Data in final administrative stage, aiming for Q2 release but dependent on BARDA protocols.
Q: Norovirus partnership and trial timeline.
A: Active discussions with partners, trial depends on funding.
Q: Interaction with Sanofi.
A: Continues productive dialogue, Sanofi sees value in COVID-19 program.
Q: Board changes rationale.
A: Added Dr. Breitmaier for clinical and regulatory expertise to navigate data milestones.
Reported results against consensus at the time of each report · Surprise is computed from the estimate on record · Data as of Nov 12, 2026