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Vaxart Q3 2026 revenue falls to $10.6M; loss widens

Topline data from Vaxart's Phase 2b COVID-19 trial, including its sentinel and main cohorts, are anticipated by mid-year 2027.

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Form Type
8-K

Rhea-AI Filing Summary

Vaxart, Inc. reported third-quarter 2026 revenue of $10.620 million and a net loss of $17.689 million. Revenue for the three months ended September 30, 2025 was $72.413 million; net loss for that period was $8.141 million. For the nine months ended September 30, 2026, revenue was $77.032 million and net loss was $26.004 million, compared with $133.019 million in revenue and a $38.718 million net loss a year earlier. Cash and cash equivalents were $35.117 million at September 30, 2026, versus $53.814 million at December 31, 2025; short-term investments were $30.427 million and $9.993 million, respectively.

Topline data from Vaxart's Phase 2b COVID-19 trial, covering a 400-person sentinel safety cohort and approximately 5,000 patients in the main cohort, are anticipated by mid-year 2027. Vaxart also expanded its intellectual property portfolio with a new European patent that further protects core intellectual property for its oral recombinant norovirus vaccine candidate and appointed Raquel “Rocky” C. Bono, M.D., Vice Admiral, U.S. Navy (Ret.), to its Board of Directors.

1 point · 0 major

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Rhea-AI Sentiment measures something else, the tone of the wording.

0 major · 2 points

How the balance works

Positive

  • Moderate pointNine-month net loss narrowed to $26.004 million from $38.718 million.

Negative

  • Moderate pointThird-quarter revenue was $10.620 million, versus $72.413 million a year earlier.
  • Moderate pointThird-quarter net loss was $17.689 million, versus $8.141 million a year earlier.

Filing Explained

Vaxart furnished its third-quarter 2026 results release with this Form 8-K; the filing says it is not deemed filed for Section 18 purposes or subject to liability under Securities Act Sections 11 and 12(a)(2). The release also is not incorporated by reference into any other Vaxart SEC filing.

Item 2.02 Results of Operations and Financial Condition Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, or exhibit attachments filed with this report.
Revenue $10.620 million Three months ended September 30, 2026; $72.413 million for the same period in 2025
Net loss $17.689 million Three months ended September 30, 2026; $8.141 million for the same period in 2025
Revenue $77.032 million Nine months ended September 30, 2026; $133.019 million for the same period in 2025
Net loss $26.004 million Nine months ended September 30, 2026; $38.718 million for the same period in 2025
Cash and cash equivalents $35.117 million As of September 30, 2026
Short-term investments $30.427 million As of September 30, 2026
sentinel safety cohort medical
"400-person sentinel safety cohort"
A sentinel safety cohort is a small initial group of trial participants treated and observed closely before a larger group is enrolled, used to detect early safety problems or unexpected side effects. Like a test run or a pilot group, it helps regulators and sponsors confirm that dosing and procedures are safe, which can affect trial timing, regulatory reviews, and the pace at which a program can advance.
unbilled receivable from government contracts financial
"Unbilled receivable from government contracts"
deferred collaboration revenue financial
"Deferred collaboration revenue"
Revenue $10.620 million Versus $72.413 million for the three months ended September 30, 2025
Net loss $17.689 million Versus $8.141 million for the three months ended September 30, 2025

FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

How much revenue did VXRT report for Q3 2026?

VXRT reported revenue of $10.620 million for the three months ended September 30, 2026. Revenue for the same period in 2025 was $72.413 million.

What was Vaxart's net loss in Q3 2026?

Vaxart reported a net loss of $17.689 million for the three months ended September 30, 2026, compared with a net loss of $8.141 million in the same 2025 period.

When does Vaxart anticipate topline COVID-19 trial data?

Vaxart anticipates topline data by mid-year 2027 from its Phase 2b COVID-19 trial, including a 400-person sentinel safety cohort and approximately 5,000 patients in the main cohort.

Who joined Vaxart's board?

Raquel “Rocky” C. Bono, M.D., Vice Admiral, U.S. Navy (Ret.), was appointed to Vaxart's Board of Directors as chair of its newly established Stockholder Engagement Committee.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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false 0000072444 0000072444 2026-11-05 2026-11-05
 
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
 
FORM 8-K
 
CURRENT REPORT
Pursuant to Section 13 or 15(d) of The Securities Exchange Act of 1934
 
Date of Report (Date of earliest event reported):
 
November 5, 2026
 
 
Vaxart, Inc.
 
 
(Exact name of registrant as specified in its charter)
 
 
 
Delaware
 
001-35285
 
59-1212264
(State or other jurisdiction of incorporation)
 
(Commission File Number)
 
(IRS Employer Identification No.)
         
310 Utah Avenue, Suite 150, South San Francisco, California
 
94080
(Address of principal executive offices)
 
(Zip Code)
 
Registrant’s telephone number, including area code:
 
(650) 550-3500
 
 
Not Applicable
 
 
(Former name or former address, if changed since last report.)
 
 
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
 
☐
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
 
☐
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
 
☐
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
 
☐
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
 
Securities registered pursuant to Section 12(b) of the Act:
 
Title of each class
 
Trading symbol
 
Name of each exchange on which registered
*
 
*
 
*
 
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
 
Emerging Growth Company          ☐
 
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.          ☐
 
* The registrant’s common stock trades exclusively on the OTCQX® Best Market under the symbol “VXRT.”
 
 

 
 
Item 2.02
Results of Operations and Financial Condition.
 
On November 5, 2026, Vaxart, Inc. (the “Company”) issued a press release (the “Press Release”) announcing its financial results for the quarter ended September 30, 2026. A copy of the Press Release is attached to this Current Report on Form 8-K as Exhibit 99.1 and, other than the quotes by Steven Lo, is incorporated herein by reference.
 
The information in this report, including Exhibit 99.1 attached hereto, is being furnished and shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or subject to the liabilities of that section or Sections 11 and 12(a)(2) of the Securities Act of 1933, as amended. The information contained herein and in the accompanying Exhibit 99.1 shall not be deemed incorporated by reference into any filing with the U.S. Securities and Exchange Commission made by Vaxart, Inc., whether made before or after the date hereof regardless of any general incorporation language in such filing.
 
 

 
 
Item 9.01
Financial Statements and Exhibits.
 
 
(d)
Exhibits
 
Exhibit No.
 
Description
99.1
 
Press Release, dated November 5, 2026.
     
104
 
Cover Page Interactive Data File (embedded within the Inline XBRL document).
 
 

 
 
SIGNATURES
 
Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
 
Date: November 5, 2026
 
VAXART, INC.
     
   
/s/ STEVEN LO
   
Steven Lo
   
President and Chief Executive Officer
 
 

Exhibit 99.1

 

Vaxart Provides Business Update and Reports Third Quarter 2026 Financial Results

 

Topline data from 400-person sentinel safety cohort and approximately 5,000 patients in main cohort Phase 2b COVID-19 trial anticipated by mid-year 2027

 

Expanded intellectual property portfolio with new European patent that further protects core IP for Vaxart's oral recombinant norovirus vaccine candidate

 

Appointed Raquel “Rocky” C. Bono, M.D., Vice Admiral, U.S. Navy (Ret.), a nationally recognized healthcare executive and physician leader to its Board of Directors

 

Live stockholder fireside chat scheduled for November 6, 2026, at 4:30 p.m. ET

 

SOUTH SAN FRANCISCO, Calif., November 5, 2026 -- Vaxart, Inc. (OTCQX: VXRT) ("Vaxart" or the "Company"), a clinical-stage biotechnology company developing oral recombinant vaccines administered via tablet, today announced its business update and financial results for the third quarter of 2026.

 

"During the third quarter, the Vaxart team worked diligently to advance our Phase 2b COVID-19 trial," said Steven Lo, Chief Executive Officer of Vaxart. "The release of the topline efficacy and safety data from the main cohort remains a top priority, and we continue to actively work toward completion of analytical testing and disclosure of the trial results, in collaboration with our partner BARDA. In parallel, we continue to reinforce our competitive positioning, recently expanding our global intellectual property portfolio with a key European patent protecting our oral recombinant norovirus vaccine candidate and derivatives thereof. Beyond our clinical work, we remain focused on expanding board governance and fostering open dialogue with our retail stockholders as highlighted by the addition of Dr. Raquel Bono to our Board as Chair of our newly established Stockholder Engagement Committee."

 

Recent Business Highlights

 

COVID-19 Program Update

 

 

●

The Company expects to release topline efficacy and safety data from the complete study, comprising the 400 participants in the sentinel safety cohort and approximately 5,000 participants in the main cohort, by mid-year 2027.

 

BARDA COVID-19 Contract Update

 

 

●

As of September 30, 2026, Vaxart has received cumulative cash payments of $278.0 million associated with the BARDA contract awarded in 2024.

 

 

 

Norovirus Vaccine Developments

 

 

●

In August 2026, Vaxart announced receipt of a new patent from the European Patent Office for key aspects of Vaxart's room-temperature stable, needle-free pill technology for the use of against norovirus. The patent extends the Company’s intellectual property protection through at least 2036 across major European jurisdictions, including Germany, France, Italy, Spain and the United Kingdom.

 

Influenza Program Developments

 

 

●

In October 2026, Vaxart announced the publication of positive preclinical study results for its second-generation vaccine candidate, VXA-H5-02, against Highly Pathogenic Avian Influenza (HPAI) H5N1. The results demonstrated complete protection against a fatal dose of the current dominant virus strain.

 

Corporate Governance Enhancements

 

 

●

In October 2026, the Company announced the appointment of Retired Vice Admiral Raquel C. Bono, M.D., to its Board of Directors. Dr. Bono, a board-certified surgeon and former Director of the Defense Health Agency, brings extensive leadership, public health and governance experience. Dr. Bono was appointed pursuant to the Cooperation Agreement Vaxart entered into with a group of its stockholders in July 2026. She will serve as Chair of the Stockholder Engagement Committee and as a member of the Nominating and Governance Committee and the Clinical and Regulatory Affairs Committee.

 

Financial Results for the Third Quarter Ended September 30, 2026

 

 

●

Cash, cash equivalents, and short-term investments totaled $65.5 million as of September 30, 2026. Vaxart currently anticipates cash runway into the second quarter of 2027. The Company remains aggressive in exploring various strategies to extend its cash runway through business development partnerships and non-dilutive funding options, with the goal of achieving its upcoming clinical and regulatory milestones and maximizing stockholder value.

 

 

●

Revenue for the third quarter of 2026 was $10.6 million, compared to $72.4 million for the third quarter of 2025. Revenue in the third quarter of 2026 and the third quarter of 2025 was primarily from government contracts related to the BARDA contract awarded in June 2024, with third quarter 2026 also including revenue recognized from the Dynavax license and collaboration agreement signed in November 2025.

 

 

●

Research and development expenses were $22.8 million for the third quarter of 2026, compared to $75.9 million for the third quarter of 2025. The decrease is primarily due to a decrease in clinical trial expenses related to our COVID-19 and norovirus vaccine candidates, personnel costs, facilities costs and manufacturing costs.

 

 

 

 

●

General and administrative expenses were $5.1 million for the third quarter of 2026, compared to $4.3 million for the third quarter of 2025. The net increase is primarily due to an increase in professional and legal fees.

 

 

●

Vaxart reported a net loss of $17.7 million for the third quarter of 2026, compared to a net loss of $8.1 million for the third quarter of 2025. Net loss per share for the third quarter of 2026 was ($0.07), compared to a net loss per share of ($0.04) for the third quarter of 2025.

 

Stockholder Fireside Chat
Vaxart will host a live stockholder fireside chat to answer frequently asked stockholder questions on Friday, November 6, 2026, at 4:30 p.m. ET.

 

A live webcast of the fireside chat will be available in the Investor section on the Company’s website at www.vaxart.com. Questions may be submitted in advance to ir@vaxart.com.

 

About Vaxart
Vaxart is a clinical-stage biotechnology company developing a range of oral recombinant vaccines based on its proprietary delivery platform. Vaxart vaccines are designed to be administered using pills that can be stored and shipped without refrigeration and eliminate the risk of needle-stick injury. Vaxart believes that its proprietary pill vaccine delivery platform is suitable to deliver recombinant vaccines, positioning the Company to develop oral versions of currently marketed vaccines and to design recombinant vaccines for new indications. Vaxart’s development programs currently include pill vaccines designed to protect against coronavirus, norovirus, and influenza, as well as a therapeutic vaccine for human papillomavirus (HPV), Vaxart’s first immune-oncology indication. Vaxart has filed broad domestic and international patent applications covering its proprietary technology and creations for oral vaccination using adenovirus and TLR3 agonists.

 

 

 

Cautionary Note Regarding Forward-Looking Statements

 

This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, that involve substantial risks and uncertainties. All statements, other than statements of historical facts, included in this press release regarding Vaxart’s strategy, prospects, plans and objectives, results and timing of results from preclinical and clinical trials, commercialization agreements and licenses, and beliefs and expectations of management are forward-looking statements, including statements contained in the quotations of Vaxart’s management in this press release. These forward-looking statements may be accompanied by such words as “should,” “believe,” “could,” “potential,” “will,” “expected,” “anticipate,” “plan,” "target," "seek," "intend," "may," "predict," "project," "would," and other words and terms of similar meaning. Examples of such statements include, but are not limited to, statements regarding the potential of VXA-H5-02 and Vaxart’s oral mucosal vaccine platform to induce protective immune responses against H5N1 or other influenza strains in humans; Vaxart’s ability to maintain or extend its intellectual property protection; Vaxart’s ability to develop and commercialize its product candidates; and Vaxart’s expectations regarding the role of its platform in influenza prevention and pandemic preparedness. These forward-looking statements are based on current expectations, estimates, forecasts, and projections about the industry and markets in which Vaxart operates as well as management’s current beliefs and assumptions. Vaxart may not actually achieve the plans, carry out the intentions, or meet the expectations or projections disclosed in the forward-looking statements, and you should not place undue reliance on these forward-looking statements. Actual results or events could differ materially from the plans, intentions, expectations, and projections disclosed in the forward-looking statements, including the possibility that Vaxart’s product candidates may not be approved by the FDA or non-U.S. regulatory authorities; that, even if approved by the FDA or non-U.S. regulatory authorities, Vaxart’s product candidates may not achieve broad market acceptance; and other risks and uncertainties described in the “Risk Factors” sections of Vaxart’s most recent Annual Report on Form 10-K and subsequent Quarterly Reports on Form 10-Q filed with the U.S. Securities and Exchange Commission, which are available on the SEC’s website at www.sec.gov. The forward-looking statements in this press release speak only as of the date of this press release. Vaxart undertakes no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events, or otherwise, except as required by applicable law.

 

Contact
Vaxart Media and Investor Relations:
FINN Partners
IR@vaxart.com

 

 

 

 

Vaxart, Inc.

Condensed Consolidated Balance Sheets

 

 

   

September 30,

   

December 31,

 
   

2026

   

2025

 
   

(Unaudited)

   

(1)

 
   

(in thousands)

 

Assets

               

Cash and cash equivalents

  $ 35,117     $ 53,814  

Short-term investments

    30,427       9,993  

Accounts receivable

    21,027       14,564  

Unbilled receivable from government contracts

    9,471       36,781  

Prepaid expenses and other assets

    30,959       21,510  

Property and equipment, net

    5,008       5,433  

Prepaid clinical services, long-term

    -       25,218  

Right-of-use assets, net

    9,386       11,432  

Intangible assets, net

    2,278       2,826  

Goodwill

    4,508       4,508  

Total assets

  $ 148,181     $ 186,079  
                 

Liabilities and stockholders’ equity

               

Accounts payable

  $ 29,775     $ 21,496  

Deferred government revenue

    57       68  

Deferred collaboration revenue

    6,322       14,976  

Accrued and other liabilities

    33,166       48,696  

Operating lease liability

    7,222       8,985  

Liability related to sale of future royalties

    5,346       4,060  

Total liabilities

    81,888       98,281  

Stockholders’ equity

    66,293       87,798  

Total liabilities and stockholders’ equity

  $ 148,181     $ 186,079  

 

 

(1)

Derived from the audited consolidated financial statements of Vaxart, Inc. for the year ended December 31, 2025, included on the Form 10-K filed with the Securities and Exchange Commission on March 13, 2026.

 

 

 

 

Vaxart, Inc.

Condensed Consolidated Statements of Operations

(Unaudited)

 

 

   

QTD

   

YTD

 
                                 
   

Three Months Ended September 30,

   

Nine Months Ended September 30,

 
   

2026

   

2025

   

2026

   

2025

 
   

( in thousands, except share and per share amounts )

 
                                 

Revenue

  $ 10,620     $ 72,413     $ 77,032     $ 133,019  

Operating expenses:

                               

Research and development

    22,829       75,947       85,996       156,426  

General and administrative

    5,074       4,277       16,318       13,942  

Total operating expenses

    27,903       80,224       102,314       170,368  

Operating loss

    -17,283       -7,811       -25,282       -37,349  

Other expense, net

    -94       -313       -352       -1,237  

Loss before income taxes

    -17,377       -8,124       -25,634       -38,586  

Provision for income taxes

    312       17       370       132  

Net loss

  $ (17,689 )   $ (8,141 )   $ (26,004 )   $ (38,718 )

Net loss per share, basic and diluted

  $ (0.07 )   $ (0.04 )   $ (0.11 )   $ (0.17 )

Shares used in computing net income (loss) per share, basic and diluted

    243,143,667       228,926,340       241,986,284       228,405,929  

 

 

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