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Dynavax Technologies (DVAX) issued a correction to its stockholder letter regarding value generation metrics, revising from "$1 billion and 104% return" to "over $900 million and 62% return" versus the S&P Biotechnology Index. The company is currently engaged in a proxy battle with Deep Track Capital, defending its strategic direction and urging shareholders to vote for its four director nominees at the June 11, 2025 Annual Meeting.

The company reported strong Q1 2025 results with total revenue of $68.2 million (34% YoY increase), including HEPLISAV-B® revenue of $65 million (36% YoY increase). HEPLISAV-B® achieved ~43% U.S. market share. Dynavax has completed 85% of its $200 million share repurchase program and announced new pipeline programs including Pandemic Influenza and Lyme Disease vaccines.

The company expects 2025 Adjusted EBITDA of at least $75 million and HEPLISAV-B® full-year revenue in the top half of $305-325 million guidance range.

Dynavax Technologies (DVAX) ha corretto la sua lettera agli azionisti riguardo ai parametri di generazione di valore, modificando da "$1 miliardo e 104% di rendimento" a "oltre $900 milioni e 62% di rendimento" rispetto all'indice S&P Biotechnology. L'azienda è attualmente impegnata in una battaglia per il voto con Deep Track Capital, difendendo la propria strategia e invitando gli azionisti a votare per i suoi quattro candidati al consiglio di amministrazione durante l'Assemblea Annuale del 11 giugno 2025.

La società ha riportato risultati solidi nel primo trimestre 2025 con ricavi totali di $68,2 milioni (aumento del 34% su base annua), inclusi ricavi da HEPLISAV-B® di $65 milioni (incremento del 36% su base annua). HEPLISAV-B® ha raggiunto circa il 43% della quota di mercato negli Stati Uniti. Dynavax ha completato l'85% del suo programma di riacquisto azionario da $200 milioni e ha annunciato nuovi programmi in pipeline, tra cui vaccini per l'influenza pandemica e la malattia di Lyme.

La società prevede un EBITDA rettificato per il 2025 di almeno $75 milioni e ricavi annuali da HEPLISAV-B® nella metà superiore della fascia di previsione tra $305 e $325 milioni.

Dynavax Technologies (DVAX) emitió una corrección en su carta a los accionistas sobre las métricas de generación de valor, revisando de "$1 mil millones y 104% de retorno" a "más de $900 millones y 62% de retorno" frente al índice S&P Biotechnology. La empresa está actualmente involucrada en una batalla de poder con Deep Track Capital, defendiendo su dirección estratégica e instando a los accionistas a votar por sus cuatro candidatos a director en la Reunión Anual del 11 de junio de 2025.

La compañía reportó sólidos resultados en el primer trimestre de 2025 con ingresos totales de $68.2 millones (un aumento interanual del 34%), incluyendo ingresos de HEPLISAV-B® de $65 millones (un incremento interanual del 36%). HEPLISAV-B® alcanzó aproximadamente el 43% de la cuota de mercado en EE. UU. Dynavax ha completado el 85% de su programa de recompra de acciones de $200 millones y anunció nuevos programas en desarrollo, incluyendo vacunas para la Influenza Pandémica y la Enfermedad de Lyme.

La compañía espera un EBITDA ajustado para 2025 de al menos $75 millones y que los ingresos anuales de HEPLISAV-B® se sitúen en la mitad superior del rango previsto de $305-325 millones.

다이나백스 테크놀로지스(DVAX)는 가치 창출 지표에 관한 주주 서한을 수정하여 "10억 달러 및 104% 수익률"에서 "9억 달러 이상 및 62% 수익률"로 S&P 바이오테크놀로지 지수 대비 수치를 변경했습니다. 회사는 현재 딥 트랙 캐피털과 대리 전쟁을 벌이고 있으며, 전략 방향을 옹호하며 2025년 6월 11일 연례 총회에서 자사의 네 명의 이사 후보에 대한 주주들의 투표를 촉구하고 있습니다.

회사는 2025년 1분기 강력한 실적을 보고했으며, 총 매출액 6,820만 달러 (전년 대비 34% 증가), HEPLISAV-B® 매출 6,500만 달러 (전년 대비 36% 증가)를 포함합니다. HEPLISAV-B®는 미국 시장 점유율 약 43%를 달성했습니다. 다이나백스는 2억 달러 규모의 자사주 매입 프로그램의 85%를 완료했으며, 팬데믹 인플루엔자 및 라임병 백신 등 신규 파이프라인 프로그램을 발표했습니다.

회사는 2025년 조정 EBITDA가 최소 7,500만 달러에 이를 것으로 예상하며, HEPLISAV-B®의 연간 매출은 3억 500만 달러에서 3억 2,500만 달러 가이던스 범위의 상위 절반에 위치할 것으로 전망합니다.

Dynavax Technologies (DVAX) a publié une correction à sa lettre aux actionnaires concernant les indicateurs de création de valeur, révisant de « 1 milliard de dollars et un rendement de 104 % » à « plus de 900 millions de dollars et un rendement de 62 % » par rapport à l'indice S&P Biotechnology. La société est actuellement engagée dans une bataille de procuration avec Deep Track Capital, défendant sa stratégie et encourageant les actionnaires à voter pour ses quatre candidats au conseil d'administration lors de l'Assemblée Générale Annuelle du 11 juin 2025.

La société a annoncé de solides résultats pour le premier trimestre 2025 avec un chiffre d'affaires total de 68,2 millions de dollars (augmentation de 34 % sur un an), comprenant un chiffre d'affaires HEPLISAV-B® de 65 millions de dollars (augmentation de 36 % sur un an). HEPLISAV-B® a atteint environ 43 % de part de marché aux États-Unis. Dynavax a réalisé 85 % de son programme de rachat d'actions de 200 millions de dollars et a annoncé de nouveaux programmes en développement, incluant des vaccins contre la grippe pandémique et la maladie de Lyme.

La société prévoit un EBITDA ajusté d'au moins 75 millions de dollars pour 2025 et un chiffre d'affaires annuel de HEPLISAV-B® dans la moitié supérieure de la fourchette prévue de 305 à 325 millions de dollars.

Dynavax Technologies (DVAX) hat eine Korrektur seines Aktionärsschreibens bezüglich der Wertschöpfungskennzahlen veröffentlicht und die Angaben von „1 Milliarde Dollar und 104 % Rendite“ auf „über 900 Millionen Dollar und 62 % Rendite“ im Vergleich zum S&P Biotechnology Index revidiert. Das Unternehmen befindet sich derzeit in einem Stimmrechtsstreit mit Deep Track Capital, verteidigt seine strategische Ausrichtung und fordert die Aktionäre auf, bei der Hauptversammlung am 11. Juni 2025 für seine vier Direktorkandidaten zu stimmen.

Das Unternehmen meldete starke Ergebnisse für das erste Quartal 2025 mit Gesamtumsatz von 68,2 Millionen Dollar (34 % Wachstum im Jahresvergleich), einschließlich HEPLISAV-B®-Umsatz von 65 Millionen Dollar (36 % Wachstum im Jahresvergleich). HEPLISAV-B® erreichte etwa 43 % Marktanteil in den USA. Dynavax hat 85 % seines Aktienrückkaufprogramms in Höhe von 200 Millionen Dollar abgeschlossen und neue Pipeline-Programme angekündigt, darunter Impfstoffe gegen Pandemie-Influenza und Lyme-Borreliose.

Das Unternehmen erwartet für 2025 ein bereinigtes EBITDA von mindestens 75 Millionen Dollar und einen HEPLISAV-B®-Jahresumsatz im oberen Bereich der Prognose von 305 bis 325 Millionen Dollar.

Positive
  • Q1 2025 revenue increased 34% YoY to $68.2 million
  • HEPLISAV-B® revenue grew 36% YoY to $65 million with 43% market share
  • Executed 85% ($172M) of $200M share repurchase program
  • Expected 2025 Adjusted EBITDA of at least $75 million
  • Pipeline expansion with new Pandemic Influenza and Lyme Disease vaccine programs
  • 203% stockholder return over past five years, outperforming vaccine peers
Negative
  • Adjusted EBITDA still negative at -$4M in Q1 2025
  • Correction of stockholder value metrics from $1B/104% return to $900M/62% return
  • Ongoing proxy battle with Deep Track Capital creating uncertainty

In the news release, Dynavax Issues Statement and Mails Letter to Stockholders Emphasizing Record Financial Results and Continued Momentum, issued 07-May-2025 by Dynavax Technologies over PR Newswire, we are advised by the company that the second paragraph, second sentence of the stockholder letter should read "Dynavax has generated over $900 million of stockholder value, returning over 62% versus the S&P Biotechnology Select Industry Index's return of -7%[2]." rather than "Dynavax has generated approximately $1 billion of stockholder value, returning over 104% versus the S&P Biotechnology Select Industry Index's return of only 14%[2]." as originally issued inadvertently. The complete, corrected release follows:

Dynavax Issues Statement and Mails Letter to Stockholders Emphasizing Record Financial Results and Continued Momentum

Deep Track's Misleading Investor Presentation Demonstrates its Single-Minded Approach to Abandon Long-Term Value Opportunities in Exchange for Short-Term Return

Urges Stockholders to Vote "FOR" All Four Dynavax Director Nominees on the GOLD Proxy Card Today

EMERYVILLE, Calif., May 7, 2025 /PRNewswire/ -- Dynavax Technologies Corporation (Nasdaq: DVAX) ("Dynavax" or the "Company"), a commercial-stage biopharmaceutical company developing and commercializing innovative vaccines, today issued the following statement in response to the investor presentation issued by Deep Track Capital ("Deep Track"):

Deep Track's investor presentation demonstrates that Deep Track fundamentally does not understand how to run a successful commercial stage biotechnology company. Deep Track's one-dimensional plan to strip-mine Dynavax ignores market realities and the clear need to have a diversified portfolio and will destroy long-term stockholder value in pursuit of a quick return. Further, Deep Track has yet to provide any actionable ideas on how to grow HEPLISAV-B®, a core pillar of its own plan, which our Board and management team are already doing with great success. In contrast, Dynavax's strategic plan is working – we have delivered returns of 203% stockholders over the last five years, far outperforming vaccine peers, which have returned 9%, and the S&P Biotechnology Select Industry Index, which has declined 17%.

Strategically investing in growth through intentional pursuit of both internal and external assets and opportunistically returning capital to stockholders are not mutually exclusive and the Board has proven that the Company's disciplined capital allocation is the right approach for Dynavax stockholders who are invested for the long term. While attacking the Company's cash position – which was earned through exponential HEPLISAV-B® growth and prudent dealmaking execution during COVID-19 – Deep Track fails to acknowledge that Dynavax is one of the few vaccine companies to return meaningful capital to stockholders. Share repurchases represent 47%1 of Dynavax's use of capital.

As Deep Track's presentation highlights, it favors a near-term payoff at considerably lower value and has no reservations about jeopardizing a strong growth platform with tremendous long-term upside. By Deep Track's own admission, each of its settlement counterproposals were conditioned on either the appointment of its underqualified fund principal, a dramatically increased share repurchase program and/or the immediate declassification of the Board – all of which clearly point to Deep Track's desire to gain control of the Board and effectuate its plan. Indeed, the repeated refrain from Deep Track and its representatives throughout our negotiations was that Deep Track required the opportunity to obtain majority turnover on the Board by 2026. Throughout months of earnest negotiation from the Dynavax Board with four different settlement proposals that offered significant Board change, Deep Track's single-minded thinking was the impediment to a resolution. It is clear that Deep Track's recent investor presentation is replete with misleading and factually inaccurate statements.

Dynavax is delivering record financial and operational results and superior value to stockholders. The successful execution of the Company's balanced strategic plan is being overseen by a highly qualified and meaningfully refreshed Board with director nominees that outmatch Deep Track's candidates in every critical area, and we are confident that Dynavax is on the right path forward.

Dynavax also mailed a letter to its stockholders in connection with its 2025 Annual Meeting of Stockholders ("Annual Meeting") urging stockholders to vote the GOLD proxy card "FOR" all four of Dynavax's highly qualified directors standing for election – Brent MacGregor, Scott Myers, Lauren Silvernail and Elaine Sun. The Annual Meeting will be held on June 11, 2025, and Dynavax stockholders of record as of April 14, 2025, will be entitled to vote at the Annual Meeting.

The full text of the letter being mailed to stockholders follows:

Dear Fellow Stockholder,

As a result of the strategic decisions made by the current Board and management team, Dynavax is in the strongest position it has ever been in, and the Company's recent financial performance demonstrates that our strategy is delivering excellent results.

Since our 2019 pivot to prioritize Dynavax's vaccine business and launch HEPLISAV-B®, we have designed a clear and thoughtful strategic plan and methodically executed against it, which has directly translated into value for you, Dynavax stockholders. Dynavax has generated over $900 million of stockholder value, returning over 62% versus the S&P Biotechnology Select Industry Index's return of -7%2.

Our record first quarter 2025 earnings results announced on May 6, once again, demonstrate we have the right plan and team in place:

    • Total revenue of $68.2 million, a 34% increase compared to $50.8 million in Q1 2024.
    • HEPLISAV-B® achieved net product revenue of $65 million, an increase of 36% compared to $47.8 million in Q1 2024. This puts Dynavax on track to achieve the top half of our full year guidance range of $305 to $325 million.
    • HEPLISAV-B® total estimated U.S. market share increased to approximately 43%, compared to approximately 41% in Q1 2024.
    • Improved Adjusted EBITDA to negative $4 million, compared to negative $7 million in Q1 2024. Dynavax continues to expect Adjusted EBITDA to be at least $75 million in 2025, demonstrating our ability to grow adjusted EBITDA at more than 2 times the rate of product revenue.
    • Executed over 85% of the $200 million share repurchase program that was implemented in November 2024, with $172 million complete as of May 5, 2025.

A critical element of Dynavax's overarching strategy is leveraging our proprietary CpG 1018 adjuvant to advance our differentiated vaccine pipeline focused on well-established antigens and biology with clear regulatory pathways in order to enable long-term top-line growth and sustained stockholder value creation. Alongside our first quarter results, we announced new pipeline programs, in addition to our ongoing shingles and plague vaccine programs:

    • Pandemic Influenza: Will support global pandemic preparedness and response efforts. Dynavax expects to initiate a Phase 1/2 study in Q2 2025.
    • Lyme Disease: There are currently no approved human vaccines for Lyme disease and we believe that our investigational Lyme disease vaccine, adjuvanted with CpG 1018, has the potential for a differentiated and best-in-class vaccine profile. Dynavax expects to initiate clinical development in 2027.

Our differentiated expertise and capabilities, plus scaling and diversifying our pipeline and commercial product portfolio through internal R&D and corporate development, has led to a proven blueprint for long-term success in biopharma to drive continued value creation.

VOTE TODAY TO HELP ENSURE DYNAVAX'S CONTINUED MOMENTUM

The current Dynavax Board, including, our nominees up for re-election this year— Brent MacGregor, Scott Myers (our Chairman), Lauren Silvernail and Elaine Sun — are uniquely equipped with the necessary expertise to continue successfully advancing Dynavax's strategy and drive long-term stockholder value. We urge you to vote "FOR" Dynavax's four director nominees on the GOLD universal proxy card today.

Deep Track's proposed changes to the Board would install unqualified nominees who want to effectuate an outsized capital return and shutter efforts to accelerate growth with internal and external opportunities. This plan would destroy the future value of our business and jeopardize the long-term potential of your investment.

Our Board and management team remain focused on what matters most – working to deliver record results and sustained growth in 2025 and beyond.

Thank you for your continued support,
The Dynavax Board of Directors

Advisors

Goldman Sachs & Co. LLC is serving as financial advisor to Dynavax and Cooley LLP is serving as legal counsel.

About Dynavax

Dynavax is a commercial-stage biopharmaceutical company developing and commercializing innovative vaccines to help protect the world against infectious diseases. The Company has two commercial products, HEPLISAV-B® vaccine (Hepatitis B Vaccine (Recombinant), Adjuvanted), which is approved in the U.S., the European Union and the United Kingdom for the prevention of infection caused by all known subtypes of hepatitis B virus in adults 18 years of age and older, and CpG 1018® adjuvant, currently used in HEPLISAV-B and multiple adjuvanted COVID-19 vaccines. For more information about our marketed products and development pipeline, visit www.dynavax.com.

Forward-Looking Statements

This communication 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, which are subject to a number of risks and uncertainties. All statements that are not historical facts are forward-looking statements. Forward-looking statements can generally be identified by the use of words such as "believe," "continue," "estimate," "expect," "will," "plan," "potential," "would" and similar expressions, or the negatives thereof, or they may use future dates. Forward-looking statements made in this document include statements regarding expected contributions from our current directors, expectations regarding delivering value for our stockholders, our future growth, potential of our differentiated technology, the timing of initiation and completion of clinical trials and expected results, market share and size of the market, expected product revenue, our business strategy and long-term performance. Actual results may differ materially from those set forth in this communication due to the risks and uncertainties inherent in our business, including, the risk that circumstances surrounding or leading up to our 2025 Annual Meeting may change, risks relating to our ability to commercialize and supply HEPLISAV-B, the risks that market size or actual demand for our products may differ from our expectations, risks related to the timing of completion and results of current clinical studies, risks related to the development and pre-clinical and clinical testing of vaccines containing CpG 1018 adjuvant, and risks related to the implementation of our long-term growth objectives, as well as other risks detailed in the "Risk Factors" section of our Quarterly Report on Form 10-Q for the three months ended March 31, 2025 and any periodic filings made thereafter, as well as discussions of potential risks, uncertainties and other important factors in our other filings with the U.S. Securities and Exchange Commission. These forward-looking statements are made as of the date hereof, are qualified in their entirety by this cautionary statement and we undertake no obligation to revise or update information herein to reflect events or circumstances in the future, even if new information becomes available. Information on Dynavax's website at www.dynavax.com is not incorporated by reference in our current periodic reports with the SEC.

Important Additional Information and Where to Find It

On April 17, 2025, the Company filed a definitive proxy statement on Schedule 14A (the "Proxy Statement") and form of accompanying GOLD proxy card with the U.S. Securities and Exchange Commission (the "SEC") in connection with its 2025 Annual Meeting and its solicitation of proxies for the Company's director nominees and for other matters to be voted on. The Company may also file other relevant documents with the SEC regarding its solicitation of proxies for the 2025 Annual Meeting. This communication is not a substitute for any proxy statement or other document that the Company has filed or may file with the SEC in connection with any solicitation by the Company. STOCKHOLDERS OF THE COMPANY ARE STRONGLY ENCOURAGED TO READ THE PROXY STATEMENT, ACCOMPANYING GOLD PROXY CARD AND OTHER RELEVANT DOCUMENTS FILED WITH, OR FURNISHED TO, THE SEC CAREFULLY AND IN THEIR ENTIRETY AS THEY CONTAIN IMPORTANT INFORMATION. Stockholders may obtain a copy of the Proxy Statement, accompanying GOLD proxy card, any amendments or supplements to the Proxy Statement and any other relevant documents filed by the Company with the SEC at no charge at the SEC's website at www.sec.gov. Copies will also be available at no charge at the Company's website at https://investors.dynavax.com/sec-filings.

Certain Information Regarding Participants

This communication is neither a solicitation of a proxy or consent nor a substitute for any proxy statement or other filings that may be made with the SEC. The Company, its directors, its director nominees and certain of its executive officers and employees may be deemed to be participants in the solicitation of proxies for the 2025 Annual Meeting. Information regarding the names of such persons and their respective direct or indirect interests in the Company, by securities holdings or otherwise, is available in the Proxy Statement, which was filed with the SEC on April 17, 2025, including in the sections captioned "Compensation Discussion and Analysis," "Summary Compensation Table," "Grants of Plan Based Awards," "Outstanding Equity Awards at Fiscal Year End," "Pay Ratio Disclosure," "Director Compensation," "Certain Transactions," "Security Ownership of Certain Beneficial Owners and Management," and "Supplemental Information Regarding Participants in the Solicitation." To the extent that the Company's directors and executive officers have acquired or disposed of securities holdings since the applicable "as of" date disclosed in the Proxy Statement, such transactions have been or will be reflected on Statements of Changes in Ownership of Securities on Form 4 or Initial Statements of Beneficial Ownership of Securities on Form 3 filed with the SEC. These documents are or will be available free of charge at the SEC's website at www.sec.gov.

Non-GAAP Financial Measures 

To supplement our financial results presented on a GAAP basis, we have included information about adjusted EBITDA, a non-GAAP financial measure. We believe the presentation of this non-GAAP financial measure, when viewed with our results under GAAP, provide analysts, investors and other third parties with insights into how we evaluate normal operational activities, including our ability to generate cash from operations, on a comparable year-over-year basis and manage our budgeting and forecasting.

Adjusted EBITDA
Adjusted EBITDA is a non-GAAP financial measure that represents GAAP net income or loss adjusted to exclude interest expense, interest income, the benefit from or provision for income taxes, depreciation, amortization, stock-based compensation, and other adjustments to reflect changes that occur in our business but do not represent ongoing operations, including loss on debt extinguishment and proxy contest costs. Adjusted EBITDA, as used by us, may be calculated differently from, and therefore may not be comparable to, similarly titled measures used by other companies.

There are several limitations related to the use of adjusted EBITDA rather than net income or loss, which is the nearest GAAP equivalent, such as:

  • adjusted EBITDA excludes depreciation and amortization, and, although these are non-cash expenses, the assets being depreciated or amortized may have to be replaced in the future, the cash requirements for which are not reflected in adjusted EBITDA;
  • adjusted EBITDA does not reflect changes in, or cash requirements for, working capital needs;
  • adjusted EBITDA does not reflect the benefit from or provision for income taxes or the cash requirements to pay taxes;
  • adjusted EBITDA does not reflect historical cash expenditures or future requirements for capital expenditures or contractual commitments;
  • we exclude stock-based compensation expense from adjusted EBITDA although: (i) it has been, and will continue to be for the foreseeable future, a significant recurring expense for our business and an important part of our compensation strategy; and (ii) if we did not pay out a portion of our compensation in the form of stock-based compensation, the cash salary expense included in operating expenses would be higher, which would affect our cash position;
  • we may exclude other expenses, from time to time, that are episodic in nature and do not directly correlate to the cost of operating our business on an ongoing basis.

The Company has not provided a reconciliation of its full‐year 2025 guidance for Adjusted EBITDA to the most directly comparable forward‐looking GAAP measures because the Company is unable to predict, without unreasonable efforts, the timing and amount of items that would be included in such a reconciliation, including, but not limited to, stock‐based compensation expense, income tax expense or provision for income taxes. These items are uncertain and depend on various factors that are outside of the Company's control or cannot be reasonably predicted. While the Company is unable to address the probable significance of these items, they could have a material impact on GAAP net income for the guidance period. A reconciliation of Adjusted EBITDA would imply a degree of precision and certainty as to these future items that does not exist and could be confusing to investors.

For Investors:

Paul Cox
pcox@dynavax.com
510-665-0499

Or

MacKenzie Partners, Inc.
Bob Marese / John Bryan
Toll-Free: 1-800-322-2885
DVAX@mackenziepartners.com 

For Media:

Dan Moore / Tali Epstein
Dynavax-CS@collectedstrategies.com

1 Use of capital from 2020 to present, excluding CapEx and SG&A expense; reflects full execution of the $200 million share repurchase program.
2 Total stockholder return from May 23, 2019, the date Dynavax announced its strategic pivot, to April 17, 2025, the date Dynavax filed its definitive proxy.

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/dynavax-issues-statement-and-mails-letter-to-stockholders-emphasizing-record-financial-results-and-continued-momentum-302449223.html

SOURCE Dynavax Technologies

FAQ

What were Dynavax (DVAX) Q1 2025 earnings results?

Dynavax reported Q1 2025 total revenue of $68.2M (34% YoY increase), with HEPLISAV-B® revenue of $65M (36% YoY increase). Adjusted EBITDA improved to -$4M from -$7M in Q1 2024.

What is the market share of Dynavax's HEPLISAV-B® vaccine?

HEPLISAV-B® achieved approximately 43% U.S. market share in Q1 2025, up from 41% in Q1 2024.

What new vaccine programs did Dynavax (DVAX) announce?

Dynavax announced two new vaccine programs: a Pandemic Influenza vaccine (Phase 1/2 study starting Q2 2025) and a Lyme Disease vaccine (clinical development expected in 2027).

How much of Dynavax's share repurchase program has been completed?

As of May 5, 2025, Dynavax has executed over 85% ($172 million) of its $200 million share repurchase program implemented in November 2024.

What is Dynavax's revenue guidance for HEPLISAV-B® in 2025?

Dynavax expects HEPLISAV-B® revenue to reach the top half of their guidance range of $305-325 million for full-year 2025.
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