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VXRT

Vaxart, Inc.

NASDAQ · Healthcare · Biotechnology · US

$0.50
+0.51%
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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
Earnings call summaryRead the full call →

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