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Vaxart Provides Business Update and Reports Third Quarter 2024 Financial Results

VXRT 11.13.2024

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Date of Upcoming Event:2024-10-01

Name of Upcoming Event:IDWeek

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Expects to complete enrollment of the 400-participant sentinel cohort for the COVID-19 Phase 2b study inNovember 2024

Solid financial position enablesVaxartto attain multiple regulatory and clinical milestones

Conference call today at4:30 p.m. ET

SOUTH SAN FRANCISCO, Calif.,Nov. 13, 2024(GLOBE NEWSWIRE) --Vaxart, Inc.(Nasdaq: VXRT) today announced its business update and financial results for the third quarter of 2024.

“Our successful initiation of sentinel cohort dosing is a testament to our rapid execution in helping to ensure that we remain on track to meet the milestones of ourBiomedical Advanced Research Development Authority(BARDA) contract,” saidSteven Lo, Vaxart’s Chief Executive Officer. “We are pleased to be nearing completion of enrollment of the sentinel cohort. Then, if theU.S. Food and Drug Administration(FDA) and independent Data and Safety Monitoring Board’s (DSMB’s) 30-day safety data review is favorable, we will initiate the 10,000-participant portion of the Phase 2b trial. Our continued progress brings us closer to our goal of demonstrating advantages of our mucosal technology against an approved mRNA vaccine.”

“On our norovirus program, we received constructive feedback from the FDA on our proposed correlate of protection and are evaluating next steps,”Mr. Loadded. “Additionally, our scientific team created potentially more potent norovirus GI.1 and GII.4 constructs compared to the constructs previously evaluated in our clinical trials. We are excited about the potential these improvements may yield and remain committed to moving forward with our norovirus program.”

Recent Business Highlights

COVID-19 Vaccine Developments

InSeptember 2024,Vaxartinitiated the 400-participant sentinel cohort of its Phase 2b trial to evaluate Vaxart’s oral pill COVID-19 vaccine candidate against an approved mRNA vaccine comparator. The sentinel cohort is being funded as part of the Phase 2b NextGen COVID-19 clinical trial, valued at up to$456 millionthrough the Rapid Response Partnership Vehicle under theU.S.government’s Project NextGen.
- Enrollment of the sentinel cohort is expected to be completed inNovember 2024. The 30-day safety data of the sentinel cohort will then be reviewed by the independent DSMB and the FDA.
- If the review of safety data by the DSMB and FDA is favorable,Vaxartexpects the study to progress to the second part of the trial in early 2025 by enrolling approximately 10,000 participants.
- The primary efficacy analysis will be performed when all participants have either discontinued or completed a study visit 12 months post-vaccination.

Norovirus Vaccine Developments

In the second half of 2024,Vaxartheld productive conversations with the FDA on its data for potential correlates of protection and next steps for Vaxart’s norovirus program.
- Based on the latest feedback, the FDA requested new clinical data before proceeding with further review of Vaxart’s potential correlate.
- Vaxartcreated additional norovirus GI.1 and GII.4 constructs that may be more potent than the constructs being evaluated in clinical trials.Vaxartis discussing regulatory feedback, clinical data on current constructs, and preclinical data generated on its new constructs with certain key opinion leaders in determining the best way to progress its norovirus program.
InOctober 2024,Vaxartpresented clinical research demonstrating the potential of its norovirus oral pill vaccine candidate at IDWeek.

Other Programs

InAugust 2024, preclinical data was published inVaccines,demonstrating the potential of Vaxart’s mucosal vaccine technology platform in enabling therapeutic vaccination against HPV-related cervical dysplasia.

Financial Results for the Third Quarter Ended September 30, 2024

Cash, cash equivalents and investments totaled$58.7 millionas ofSeptember 30, 2024.Vaxartcontinues to anticipate cash runway into 2026.
Vaxartreported a net loss of $14.1 million for the third quarter of 2024, compared to$17.4 millionfor the third quarter of 2023. Net loss per share for the third quarter of 2024 was $0.06, compared to a net loss per share of $0.11 for the third quarter of 2023.
Revenue for the third quarter of 2024 was $4.9 million, compared to $2.1 million for the third quarter of 2023. Revenue in the third quarter of 2024 was primarily from government contracts related to the BARDA contracts awarded inJanuary 2024andJune 2024. Revenue in the third quarter of 2023 was primarily from revenue recognized for work performed under Vaxart’s grant from theBill & Melinda Gates Foundationand non-cash royalty revenue from increased sales of Inavir inJapan.
Research and development expenses were $15.1 million for the third quarter of 2024, compared to $15.0 million for the third quarter of 2023. The R&D expenses in the latest quarter were primarily due to increases in clinical trial expenses related to Vaxart’s COVID-19 vaccine candidate and preclinical expenses across multiple programs and facilities expenses, partially offset by decreases in clinical trial expenses related to Vaxart’s norovirus vaccine candidate, stock-based compensation expenses and personnel-related costs, and manufacturing expenses.
General and administrative expenses were$4.3million for the third quarter of 2024, compared to $4.9 million for the third quarter of 2023. The decrease was primarily due to decreases in stock-based compensation expense and directors’ and officers’ insurance costs, partially offset by increases in legal and other professional fees.

Conference CallTheVaxartsenior management team will host a conference call to discuss the business update and financial results for the third quarter of 2024 today, beginning at4:30 p.m. ET.

The conference call can be accessed using the following information:

Webcast:Click hereDate:Wednesday, November 13, 2024–4:30 p.m. ETDomestic: (877) 407-0832International: (201) 689-8433Conference ID: 13749666

Investors may submit written questions in advance of the conference call toir@vaxart.com.

A replay of the webcast will be available for 30 days on Vaxart’s website atwww.vaxart.comfollowing the conclusion of the event.

AboutVaxartVaxartis a clinical-stage biotechnology company developing a range of oral recombinant vaccines based on its proprietary delivery platform.Vaxartvaccines are designed to be administered using pills that can be stored and shipped without refrigeration and eliminate the risk of needle-stick injury.Vaxartbelieves 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.Vaxarthas 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 StatementsThis press release contains forward-looking statements that involve substantial risks and uncertainties. All statements, other than statements of historical facts, included in this press release regardingVaxart'sstrategy, prospects, plans and objectives, receipt of funding from BARDA, results from preclinical and clinical trials and the timing of such results and such trials, commercialization agreements and licenses, and beliefs and expectations of management are forward-looking statements. These forward-looking statements may be accompanied by such words as “should,” “believe,” “could,” “potential,” “will,” “expected,” “anticipate,” “plan,” and other words and terms of similar meaning. Examples of such statements include, but are not limited to, statements relating to Vaxart’s receipt of funding from BARDA for the Phase 2b study (or for any other purpose);Vaxart'sability to develop and commercialize its product candidates, including its vaccine booster products;Vaxart'sexpectations regarding clinical results and trial data, including their design, and the timing of such trials and of receiving and reporting such clinical results and trial data; Vaxart’s expectations regarding timing of enrollment in studies; andVaxart'sexpectations with respect to the effectiveness of its product candidates and the potential of its vaccine pill platform.Vaxartmay 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 thatVaxartmakes, including uncertainties inherent in research and development, including the ability to meet anticipated clinical endpoints, commencement, and/or completion dates for clinical trials, regulatory submission dates, regulatory approval dates, and/or launch dates, as well as the possibility of unfavorable new clinical data and further analyses of existing clinical data; the risk that clinical trial data are subject to differing interpretations and assessments by regulatory authorities; whether regulatory authorities will be satisfied with the design of and results from the clinical studies; 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 thatVaxart'sproduct 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'sproduct candidates may not achieve broad market acceptance; that aVaxartcollaborator may not attain development and commercial milestones; thatVaxartor its partners may experience manufacturing issues and delays due to events within, or outside of,Vaxart'sor 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; thatVaxartmay not be able to obtain, maintain, and enforce necessary patent and other intellectual property protection; thatVaxart'scapital resources may be inadequate;Vaxart'sability to resolve pending legal matters;Vaxart'sability to obtain sufficient capital to fund its operations on terms acceptable toVaxart, if at all; the impact of government healthcare proposals and policies; competitive factors; and other risks described in the "Risk Factors" sections ofVaxart'sQuarterly and Annual Reports filed with theU.S. Securities and Exchange Commission.Vaxartdoes not assume any obligation to update any forward-looking statements, except as required by law.Contact

Vaxart Media and Investor RelationsMatt SteinbergFINN PartnersIR@vaxart.com(646) 871-8481

Vaxart, Inc.
Condensed Consolidated Balance Sheets

	September 30,			December 31,
		2024			2023
	(Unaudited)				(1)
			(in thousands)
Assets
Cash and cash equivalents	$	22,035		$	34,755
Investments in marketable debt securities		36,676			4,958
Accounts receivable		591			3,008
Unbilled receivable from government contracts		3,085			-
Prepaid expenses and other assets		4,911			3,741
Property and equipment, net		9,476			11,731
Long-term prepaid clinical services		60,116			-
Right-of-use assets, net		21,536			24,840
Intangible assets, net		3,740			4,289
Goodwill		4,508			4,508
Total assets	$	166,674		$	91,830

Liabilities and stockholders’ equity
Accounts payable	$	2,524		$	1,584
Deferred government revenue		65,447			-
Accrued and other liabilities		7,185			5,927
Operating lease liability		18,201			20,088
Liability related to sale of future royalties		4,875			6,426
Total liabilities		98,232			34,025
Stockholders’ equity		68,442			57,805
Total liabilities and stockholders’ equity	$	166,674		$	91,830

(1) Derived from the audited consolidated financial statements ofVaxart, Inc.for the year endedDecember 31, 2023, included on the Form 10-K filed with theSecurities and Exchange CommissiononMarch 14, 2024.

Vaxart, Inc.
Condensed Consolidated Statements of Operations
(Unaudited)

	Three Months EndedSeptember 30,						Nine Months EndedSeptember 30,
		2024			2023			2024			2023
	(in thousands, except share and per share amounts)

Revenue	$	4,933		$	2,101		$	13,515		$	4,134
Operating expenses:
Research and development		15,066			15,002			51,559			53,437
General and administrative		4,342			4,921			16,757			17,144
Total operating expenses		19,408			19,923			68,316			70,581
Operating loss		(14,475	)		(17,822	)		(54,801	)		(66,447	)
Other income (expense), net		413			461			(78	)		1,444
Loss before income taxes		(14,062	)		(17,361	)		(54,879	)		(65,003	)
Provision for income taxes		18			39			84			87
Net loss	$	(14,080	)	$	(17,400	)	$	(54,963	)	$	(65,090	)
Net loss per share, basic and diluted	$	(0.06	)	$	(0.11	)	$	(0.28	)	$	(0.45	)
Shares used in computing net loss per share, basic and diluted		227,452,883			152,026,112			193,655,660			145,810,175

Source: Vaxart, Inc.

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