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Vaxart (Nasdaq: VXRT) sees directors re-elected but executive pay vote fails

Filing Impact
(Moderate)
Filing Sentiment
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

Vaxart, Inc. reported the results of its 2026 annual meeting of stockholders held on July 16, 2026. Proxies representing approximately 45.7% of outstanding common shares constituted a quorum. Stockholders elected six directors to serve until the 2027 annual meeting and ratified the selection of WithumSmith+Brown, PC as independent registered public accounting firm for the year ending December 31, 2026. However, stockholders did not approve, on a non-binding, advisory basis, the compensation of the named executive officers, with 46,024,068 votes for, 51,842,781 against and 2,300,962 abstentions, plus 10,463,289 broker non-votes.

The company also described its focus as a clinical-stage biotechnology company developing oral recombinant pill vaccines, including a Phase 2b trial of its oral COVID-19 vaccine candidate supported in part by Project NextGen and the RRPV Consortium.

Positive

  • None.

Negative

  • Stockholders rejected the 2026 non-binding say-on-pay proposal on executive compensation, with 51,842,781 votes against versus 46,024,068 votes for and 2,300,962 abstentions, indicating a majority vote against the company’s current named executive officer pay program.
Item 5.07 Submission of Matters to a Vote of Security Holders Governance
Results of a shareholder vote on proposals at an annual or special meeting.
Item 7.01 Regulation FD Disclosure Disclosure
Material non-public information disclosed under Regulation Fair Disclosure, often investor presentations or guidance.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
Quorum represented 45.7% Proxies representing 45.7% of outstanding common stock were submitted for the 2026 annual meeting
Votes for James B. Breitmeyer as director 86,985,391 Votes cast for election of James B. Breitmeyer at the 2026 annual meeting
Votes for auditor ratification 80,448,931 Shares voting in favor of WithumSmith+Brown, PC as independent registered public accounting firm for 2026
Votes against say-on-pay 51,842,781 Shares voting against the non-binding advisory proposal on named executive officer compensation
Votes for say-on-pay 46,024,068 Shares voting in favor of the non-binding advisory proposal on named executive officer compensation
broker non-votes regulatory
"Votes For | Votes Against | Abstentions | Broker Non-Votes"
Broker non-votes occur when a brokerage firm is unable to vote on a shareholder’s behalf during a company election or decision because the shareholder has not given specific voting instructions, and the broker is not allowed or chooses not to vote on certain matters. They are important because they can affect the outcome of votes, especially when the results are close, by effectively reducing the total number of votes cast.
non-binding, advisory basis regulatory
"Stockholders did not approve, on a non-binding, advisory basis, the compensation"
A non-binding, advisory basis means a recommendation or decision that carries no legal force and does not obligate the parties to act; it’s similar to a friendly suggestion rather than a signed promise. For investors, this matters because such guidance can influence market expectations and management plans but offers no guarantee of follow-through, so investors should treat it as informative input rather than a firm commitment.
say-on-pay regulatory
"also known as “say-on-pay”"
A say-on-pay is a shareholder vote that gives investors a chance to approve or disapprove a company’s executive compensation packages, typically held at annual meetings. It matters because the vote signals investor satisfaction with how leaders are paid—like customers rating how well managers are rewarded—and can push boards to change pay plans, reducing governance risk and affecting investor confidence and stock value even though the vote is usually advisory rather than legally binding.
Phase 2b clinical trial medical
"Vaxart’s Phase 2b clinical trial of its oral pill COVID-19 vaccine candidate"
A phase 2b clinical trial is a mid-stage medical study that tests whether a new treatment works and which dose is best by enrolling a larger group of patients than earlier phase 2 studies. For investors, its results are a key signal of a drug’s real-world effectiveness and safety, and can strongly influence the chances of later regulatory approval, future funding needs, and a company’s stock outlook—like a larger pilot test before full rollout.
sentinel safety cohort medical
"the 400-participant sentinel safety cohort, the approximately 5,000-participant main 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.
Project NextGen/BARDA/RRPV award medical
"availability, permitted uses and sufficiency of funding under the Project NextGen/BARDA/RRPV award"

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

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FAQ

What were the main outcomes of Vaxart (VXRT) 2026 annual meeting?

Vaxart’s 2026 annual meeting elected six directors, ratified WithumSmith+Brown, PC as independent auditor, and saw stockholders reject the non-binding say-on-pay proposal on executive compensation. Proxies representing about 45.7% of outstanding common shares were submitted, constituting a quorum for the meeting.

Did Vaxart (VXRT) stockholders approve the 2026 say-on-pay proposal?

No. Vaxart stockholders did not approve the 2026 non-binding, advisory say-on-pay proposal. The vote was 46,024,068 shares for, 51,842,781 against, and 2,300,962 abstentions, with an additional 10,463,289 broker non-votes recorded on the executive compensation item.

How many Vaxart (VXRT) shares were represented at the 2026 annual meeting?

Proxies submitted represented approximately 45.7% of Vaxart’s outstanding common stock entitled to vote. This level of representation constituted a quorum, allowing the company to conduct official business and vote on director elections, auditor ratification, and the advisory say-on-pay proposal.

Which auditor did Vaxart (VXRT) stockholders ratify for 2026 and by what vote?

Stockholders ratified WithumSmith+Brown, PC as Vaxart’s independent registered public accounting firm for the year ending December 31, 2026. The vote totaled 80,448,931 shares for, 19,724,442 against, and 10,457,727 abstentions, with no broker non-votes reported on this ratification proposal.

What clinical programs did Vaxart (VXRT) highlight around the annual meeting results?

Vaxart emphasized its clinical-stage pipeline of oral recombinant pill vaccines, including a Phase 2b trial of its oral COVID-19 vaccine candidate with a 400-participant sentinel safety cohort and about 5,000-participant main cohort, supported in part by Project NextGen and the RRPV Consortium, with complete study data anticipated in 2027.
false 0000072444 0000072444 2026-07-16 2026-07-16
 
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): July 16, 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 150South San FranciscoCalifornia
 
94080
(Address of principal executive offices)
 
(Zip Code)
 
Registrant’s telephone number, including area code: (650550-3500
 
 
 
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 is quoted on the OTCQX® Best Market under the symbol “VXRT.”
 

 
Item 5.07
Submission of Matters to a Vote of Security Holders.
 
On July 16, 2026, Vaxart, Inc. (the “Company”) held the Company’s 2026 annual meeting of stockholders (the “Annual Meeting”). Proxies had been submitted by stockholders representing approximately 45.7% of the shares of the Company’s common stock outstanding and entitled to vote, which constituted a quorum. At the Annual Meeting, the Company’s stockholders voted on three Proposals, each of which is described in more detail in the proxy statement for the Annual Meeting (the “Proxy Statement”).
 
The following is a brief description of each matter voted upon and the results, including the number of votes cast for and against each matter and, if applicable, the number of abstentions and broker non-votes with respect to each matter. Proxies for the Annual Meeting were solicited pursuant to Section 14(a) of the Securities Exchange Act of 1934, as amended.
 
Proposal 1. Stockholders elected the six nominees for directors to serve until the Company’s 2027 annual meeting of stockholders or until their successors are duly elected and qualified. The voting results were as follows:
 
Director Name
 
Votes For
 
Votes Withheld
 
Broker Non-Votes
James B. Breitmeyer, M.D., Ph.D.
 
86,985,391
 
13,060,491
 
10,585,218
Kevin P. Finney
 
80,409,424
 
19,636,458
 
10,585,218
Elaine J. Heron, Ph.D.
 
51,372,172
 
48,672,711
 
10,586,217
Steven Lo
 
50,272,817
 
49,772,065
 
10,586,218
W. Mark Watson, C.P.A.
 
77,497,037
 
22,548,845
 
10,585,218
David Wheadon, M.D.
 
51,931,124
 
48,113,758
 
10,586,218
 
Proposal 2. Stockholders ratified the selection by the Audit Committee of WithumSmith+Brown, PC as the Company’s independent registered public accounting firm for the year ending December 31, 2026. The voting results were as follows:
 
Votes For
 
Votes Against
 
Abstentions
 
Broker Non-Votes
80,448,931
 
19,724,442
 
10,457,727
 
-
 
Proposal 3. Stockholders did not approve, on a non-binding, advisory basis, the compensation of the Company’s named executive officers as disclosed in the Proxy Statement. The voting results were as follows:
 
Votes For
 
Votes Against
 
Abstentions
 
Broker Non-Votes
46,024,068
 
51,842,781
 
2,300,962
 
10,463,289
 
Item 7.01
Regulation FD Disclosure.
 
On July 17, 2026, the Company issued a press release announcing the voting results of the Annual Meeting. A copy of the press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K.
 
The information in this Item 7.01, and Exhibit 99.1 attached hereto, is being furnished and shall not be deemed “filed” for the purposes of Section 18 of the Exchange Act, or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, regardless of any general incorporation language in such filing.
 
Item 9.01
Financial Statements and Exhibits.
 
Exhibit No.
 
Description
99.1
 
Press Release, dated July 17, 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, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
 
Date: July 17, 2026
 
VAXART, INC.
 
 
 
 
By:
/s/ Steven Lo
 
 
Steven Lo
 
 
President and Chief Executive Officer
 
 

Exhibit 99.1

 

Vaxart Announces Results of Annual Meeting of Stockholders

 

SOUTH SAN FRANCISCO, Calif., July 17, 2026 -- Vaxart, Inc. (Nasdaq: VXRT) (“Vaxart” or the “Company”), a clinical-stage biotechnology company developing a range of oral recombinant pill vaccines based on its proprietary delivery platform, yesterday held its Annual Meeting of Stockholders (the “Annual Meeting”) in a virtual-only format. Results from the Annual Meeting indicate that two proposals were approved and one proposal was rejected by Vaxart stockholders.

 

Stockholders voted in favor of the following proposals in alignment with the Board of Directors’ recommendations:

 

 

Election of six director nominees to serve until the 2027 Annual Meeting of Stockholders

 

Ratification of WithumSmith+Brown, PC as Vaxart’s independent registered public accounting firm

 

Stockholders did not approve, on a non-binding, advisory basis, the compensation of the Company’s named executive officers as disclosed in the proxy statement for the Annual Meeting, also known as “say-on-pay”.

 

The final results will be reported on a Current Report on Form 8-K to be filed by Vaxart with the U.S. Securities and Exchange Commission.

 

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.

 


 

Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 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 from preclinical and clinical trials and the timing of such results, and beliefs and expectations of management, including statements regarding Vaxart’s Phase 2b clinical trial of its oral pill COVID-19 vaccine candidate, the 400-participant sentinel safety cohort, the approximately 5,000-participant main cohort, further analyses of trial data, anticipated timing of complete study data, and funding under Project NextGen and the RRPV Consortium, are forward-looking statements. These forward-looking statements may be accompanied by such words as "should," "believe," "could," "potential," "will," "expected," “anticipate,” "plan," “intend,” “may,” “estimate,” “approximately,” “designed,” “powered,” “subject to,” and other words and terms of similar meaning. Examples of such statements include, but are not limited to, statements relating to Vaxart's ability to develop its product candidates and oral pill vaccine platform; Vaxart's expectations regarding clinical results and trial data, and the timing of receiving and reporting such clinical results and trial data, including further analyses of the sentinel safety cohort and complete study data anticipated in 2027; Vaxart’s expectations regarding the design, powering, conduct, completion and analysis of its Phase 2b COVID-19 trial and main cohort; and Vaxart’s expectations with respect to the safety, tolerability, efficacy, relative efficacy, immunogenicity and potential regulatory significance of its product candidates, as well as the availability, permitted uses and sufficiency of funding under the Project NextGen/BARDA/RRPV award. These forward-looking statements are based on Vaxart’s current expectations and assumptions as of the date of this press release. 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. Various important factors could cause actual results or events to differ materially from the forward-looking statements that Vaxart makes, including uncertainties inherent in research and development, including the ability to meet anticipated clinical endpoints, retain participants, collect follow-up data, generate sufficient evaluable cases and events, and complete, unblind, analyze and report data from the Phase 2b trial, including the main cohort, in the expected timeframes, as well as the possibility of unfavorable new clinical data and further analyses of existing clinical data, including analyses that may differ from or not confirm the topline data from the sentinel safety cohort or may not support conclusions regarding safety, tolerability, immunogenicity, efficacy or relative efficacy; the risk that clinical trial data, including data from the sentinel safety cohort and main cohort, are subject to differing interpretations and assessments by Vaxart, investigators, independent safety reviewers, funding agencies, regulatory authorities and other third parties; whether regulatory authorities will be satisfied with the design of and results from the clinical studies, including the study’s comparator, endpoints, statistical assumptions, strain selection, safety database and efficacy analyses; decisions by regulatory authorities impacting labeling, manufacturing processes, and safety that could affect the availability or commercial potential of any product candidate, including the possibility that Vaxart's product candidates may not be approved, authorized or licensed by the FDA or non-U.S. regulatory authorities; and that results from the Phase 2b trial may not be sufficient to support regulatory submissions, regulatory interactions, approval, authorization, licensure or commercialization of Vaxart’s oral pill COVID-19 vaccine candidate; risks related to government funding for the Phase 2b trial, including whether amounts under the Project NextGen/BARDA/RRPV award will be available, released, reimbursed or sufficient in the amounts or at the times expected, and whether the award may be modified, reduced, delayed, suspended or terminated or subject to conditions, audits or other compliance requirements; that Vaxart or its partners may experience manufacturing, supply, storage, shipment, stability, quality control or quality assurance issues and delays due to events within, or outside of, Vaxart's or its partners' control; difficulties in production, particularly in scaling up initial production, including difficulties with production costs and yields, quality control, including stability of the product candidate and quality assurance testing, shortages of qualified personnel or key raw materials, and compliance with strictly enforced federal, state, and foreign regulations; Vaxart's ability to obtain sufficient capital to fund its operations on terms acceptable to Vaxart, if at all, including expenses not covered by government funding; the impact of changes in government public-health, procurement and funding priorities; changes in COVID-19 incidence, circulating variants, vaccination recommendations and market demand; and competition from approved and investigational COVID-19 vaccines and other vaccine technologies; and other risks described in the “Risk Factors” sections of Vaxart’s most recent Annual Report on Form 10-K, Quarterly Reports on Form 10-Q and other filings filed with or furnished to the SEC. Vaxart does not assume any obligation to update any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law.

 

Contact

VaxartMedia and Investor Relations         

FINN Partners

IR@vaxart.com

 

Filing Exhibits & Attachments

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