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Novavax 2024-2025 Formula COVID-19 Vaccine Available at Major Pharmacies Across the U.S.

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Novavax (Nasdaq: NVAX) announced the availability of its updated 2024-2025 Formula COVID-19 Vaccine at major U.S. pharmacies.

This protein-based vaccine, approved under Emergency Use Authorization (EUA) by the FDA on August 30, 2024, targets the JN.1 strain and shows cross-reactivity with other strains.

It's formulated for individuals aged 12 and older and is available in pre-filled syringes at CVS, Rite Aid, Walgreens, Costco, Sam's Club, and other retailers.

Novavax has expanded its distribution network, more than doubling the locations from last year. Important safety information includes risks of myocarditis and pericarditis, and common adverse reactions like injection site pain and fatigue.

Novavax (Nasdaq: NVAX) ha annunciato la disponibilità della sua nuova Vaccino COVID-19 Formula 2024-2025 nelle principali farmacie degli Stati Uniti.

Questo vaccino a base di proteine, approvato sotto l'Autorizzazione all'Uso di Emergenza (EUA) dalla FDA il 30 agosto 2024, si concentra sul ceppo JN.1 e mostra reattività incrociata con altri ceppi.

È formulato per individui di età pari o superiore a 12 anni ed è disponibile in siringhe pre-riempite presso CVS, Rite Aid, Walgreens, Costco, Sam's Club e altri rivenditori.

Novavax ha ampliato la sua rete di distribuzione, raddoppiando le sedi rispetto all'anno scorso. Informazioni importanti sulla sicurezza includono i rischi di miocardite e pericardite, e reazioni avverse comuni come dolore nel sito di iniezione e affaticamento.

Novavax (Nasdaq: NVAX) anunció la disponibilidad de su nueva Vacuna COVID-19 Fórmula 2024-2025 en las principales farmacias de EE. UU.

Esta vacuna basada en proteínas, aprobada bajo la Autorización de Uso de Emergencia (EUA) por la FDA el 30 de agosto de 2024, tiene como objetivo la cepa JN.1 y muestra reactividad cruzada con otras cepas.

Está formulada para personas de 12 años o más y está disponible en jeringas precargadas en CVS, Rite Aid, Walgreens, Costco, Sam's Club y otros minoristas.

Novavax ha ampliado su red de distribución, más que duplicando los lugares en comparación con el año pasado. La información importante de seguridad incluye riesgos de miocarditis y pericarditis, así como reacciones adversas comunes como dolor en el sitio de inyección y fatiga.

노바백스 (Nasdaq: NVAX)는 주요 미국 약국에서 2024-2025년도 COVID-19 백신 포뮬러의 가용성을 발표했습니다.

이 단백질 기반 백신은 2024년 8월 30일 FDA의 긴급 사용 승인 (EUA)을 받았으며, JN.1 변이를 목표로 하고 있으며 다른 변이에 대해서도 교차 반응성을 보입니다.

12세 이상의 개인을 위해 제조되었으며, CVS, Rite Aid, Walgreens, Costco, Sam's Club 및 기타 소매업체에서 미리 채워진 주사기로 제공됩니다.

노바백스는 유통 네트워크를 확장하여 작년보다 위치를 두 배 이상 늘렸습니다. 중요한 안전 정보에는 심근염 및 심낭염의 위험과 주사 부위 통증 및 피로와 같은 일반적인 부작용이 포함됩니다.

Novavax (Nasdaq: NVAX) a annoncé la disponibilité de son nouveau Vaccin COVID-19 Formule 2024-2025 dans les principales pharmacies américaines.

Ce vaccin à base de protéines, approuvé le 30 août 2024 par la FDA sous Autorisation d'Utilisation d'Urgence (EUA), cible la souche JN.1 et montre une réactivité croisée avec d'autres souches.

Il est formulé pour les individus âgés de 12 ans et plus et est disponible en seringues pré-remplies chez CVS, Rite Aid, Walgreens, Costco, Sam's Club et d'autres détaillants.

Novavax a élargi son réseau de distribution, doublant ainsi le nombre de points de vente par rapport à l'année dernière. Les informations importantes sur la sécurité incluent les risques de myocardite et de péricardite, ainsi que des réactions indésirables courantes telles que douleur au site d'injection et fatigue.

Novavax (Nasdaq: NVAX) hat die Verfügbarkeit seines aktualisierten COVID-19 Impfstoffs 2024-2025 in großen US-Apotheken bekannt gegeben.

Dieser proteinbasierte Impfstoff, der am 30. August 2024 von der FDA unter Notzulassung (EUA) genehmigt wurde, richtet sich gegen den JN.1 Stamm und zeigt Kreuzreaktivität mit anderen Stämmen.

Er ist für Personen ab 12 Jahren formuliert und in vorgefüllten Spritzen bei CVS, Rite Aid, Walgreens, Costco, Sam's Club und anderen Einzelhändlern erhältlich.

Novavax hat sein Vertriebsnetz erweitert und die Standorte im Vergleich zum letzten Jahr mehr als verdoppelt. Wichtige Sicherheitsinformationen umfassen Risiken für Myokarditis und Perikarditis sowie häufige Nebenwirkungen wie Schmerzen an der Injektionsstelle und Müdigkeit.

Positive
  • Emergency Use Authorization (EUA) received from the FDA.
  • Exclusive protein-based COVID-19 vaccine option in the U.S. this fall.
  • Expanded distribution network, more than doubling the locations from last year.
Negative
  • Risks of myocarditis and pericarditis associated with the vaccine.
  • Common adverse reactions include injection site pain, fatigue, and headaches.

Novavax's 2024-2025 Formula COVID-19 vaccine rollout marks a significant development in the ongoing pandemic response. As the only protein-based option available this fall, it offers a distinct advantage in a market dominated by mRNA vaccines. The expanded distribution network, now including major pharmacy chains, should boost accessibility and potentially increase market share.

The vaccine's demonstrated cross-reactivity against current virus variants could be a key selling point. However, investors should note that Emergency Use Authorization status still carries some uncertainty. The pre-filled syringe presentation may improve ease of use, potentially driving adoption among healthcare providers and consumers.

While this news is generally positive for Novavax, the impact on financials will depend on actual uptake rates and competition from established players. The safety warnings, particularly regarding myocarditis and pericarditis risks, warrant monitoring as they could affect public perception and uptake.

Novavax's protein-based vaccine offers a crucial alternative in the COVID-19 vaccine landscape. Its targeting of the JN.1 "parent strain" and cross-reactivity with current variants demonstrate a forward-thinking approach to vaccine development. This could provide broader protection against evolving strains, a significant advantage in ongoing pandemic management.

The protein-based technology may appeal to individuals hesitant about mRNA platforms, potentially increasing overall vaccination rates. However, the reported risks of myocarditis and pericarditis need careful consideration. These side effects, while rare, could impact public perception and acceptance.

The pre-filled syringe presentation is a notable improvement, likely to reduce administration errors and enhance convenience. This could be particularly beneficial in mass vaccination settings, potentially accelerating distribution efforts.

The widespread availability of Novavax's updated COVID-19 vaccine through major pharmacy chains represents a significant step in public health strategy. This expanded access could help maintain vaccination momentum as public attention to COVID-19 wanes. The protein-based formulation provides a valuable option for those who have hesitated to receive mRNA vaccines, potentially increasing overall vaccination rates.

However, the continued reliance on Emergency Use Authorization might raise questions about long-term vaccine strategy. Public health officials will need to balance communication about the vaccine's benefits with transparent discussion of known risks, particularly regarding myocarditis and pericarditis.

The cross-reactivity against current variants is promising for ongoing pandemic management. Yet, the effectiveness against future mutations remains uncertain. Continued surveillance and potential reformulation may be necessary to maintain protection against evolving strains.

  • Doses of Novavax's 2024-2025 Formula COVID-19 vaccine now available at thousands of locations nationwide
  • Novavax's updated vaccine is the only protein-based option available in the U.S. this fall for individuals aged 12 and older

GAITHERSBURG, Md., Sept. 13, 2024 /PRNewswire/ -- Novavax, Inc. (Nasdaq: NVAX), a global company advancing protein-based vaccines with its Matrix-M™ adjuvant, today announced that doses of the Novavax COVID-19 Vaccine, Adjuvanted (2024-2025 Formula) (NVX-CoV2705) to prevent COVID-19 in individuals aged 12 and older are in stock  at major pharmacy retailers across the U.S.

Through agreements with pharmacies, Novavax's updated vaccine is expected to be widely available in locations including, but not limited to, CVS Pharmacy, Rite Aid, Walgreens, Costco, Publix, Sam's Club, Kroger, Meijer, hundreds of other regional grocers and thousands of independent pharmacies. Novavax's updated vaccine received Emergency Use Authorization (EUA) on August 30, 2024 from the U.S. Food and Drug Administration (FDA).

"We have worked hard to ensure greater ease of access for consumers this vaccination season by more than doubling the number of locations stocking our vaccine compared to last year and offering a more convenient presentation in a pre-filled syringe," said John C. Jacobs, President and Chief Executive Officer, Novavax. "Our vaccine targets JN.1, the 'parent strain' of those currently circulating, and our vaccine has demonstrated cross-reactivity against JN.1 lineage viruses, including KP.2.3, KP.3, KP.3.1.1 and LB.1.1"

Novavax's vaccine is the only protein-based option available in the U.S. this fall and is in pre-filled syringe presentation. Doses of Novavax's vaccine can be located on us.novavaxcovidvaccine.com.

AUTHORIZED USE IN THE U.S.
Novavax COVID-19 Vaccine, Adjuvanted (2024-2025 Formula) has not been approved or licensed by the FDA but has been authorized for emergency use by the FDA, under an EUA to prevent Coronavirus Disease 2019 (COVID-19) for use in individuals 12 years of age and older. Refer to the full Fact Sheet for information about the Novavax COVID-19 Vaccine, Adjuvanted.

The EUA of this product will remain in effect for the duration of the COVID-19 EUA declaration justifying emergency use of the product, unless the authorization is revoked sooner.

VACCINE AUTHORIZATION (U.S.)
Novavax COVID-19 Vaccine, Adjuvanted (2024-2025 Formula) is indicated for active immunization to prevent coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in individuals 12 years of age and older.

IMPORTANT SAFETY INFORMATION
Contraindications

  • Do not administer the Novavax COVID-19 Vaccine, Adjuvanted to individuals with a known history of a severe allergic reaction (e.g., anaphylaxis) to any component of the Novavax COVID-19 Vaccine, Adjuvanted.

Warnings and Precautions

  • Management of Acute Allergic Reactions: Appropriate medical treatment must be immediately available to manage potential anaphylactic reactions following administration of the Novavax COVID-19 Vaccine, Adjuvanted.
  • Myocarditis and Pericarditis: Clinical trials data provide evidence for increased risks of myocarditis and pericarditis following administration of Novavax COVID-19 Vaccine, Adjuvanted.
  • Syncope (fainting): may occur in association with administration of injectable vaccines. Procedures should be in place to avoid injury from fainting.
  • Altered Immunocompetence: Immunocompromised persons, including individuals receiving immunosuppressant therapy, may have a diminished immune response to the Novavax COVID-19 Vaccine, Adjuvanted.
  • Limitations of Vaccine Effectiveness: The Novavax COVID-19 Vaccine, Adjuvanted may not protect all vaccine recipients.

Adverse Reactions
Solicited adverse reactions included: Injection site pain/tenderness, fatigue/malaise, muscle pain, headache, joint pain, nausea/vomiting, injection site redness, injection site swelling and fever.

Reporting Adverse Events and Vaccine Administration Errors

The vaccination provider is responsible for mandatory reporting of certain adverse events to the Vaccine Adverse Event Reporting System (VAERS) online at https://vaers.hhs.gov/reportevent.html, by calling 1-800-822-7967 or send an email to info@vaers.org.

About the Novavax COVID-19 2024-2025 Formula (NVX-CoV2705) 
NVX-CoV2705 is an updated version of Novavax's prototype COVID-19 vaccine (NVX-CoV2373) formulated to target the JN.1 variant. It is a protein-based vaccine made by creating copies of the surface spike protein of SARS-CoV-2 that causes COVID-19. With Novavax's unique recombinant nanoparticle technology, the non-infectious spike protein serves as the antigen that primes the immune system to recognize the virus, while Novavax's Matrix-M adjuvant enhances and broadens the immune response. The vaccine is packaged as a ready-to-use liquid formulation and is stored at 2° to 8°C, enabling the use of existing vaccine supply and cold chain channels. 

About Matrix-M™ Adjuvant
When added to vaccines, Novavax's patented saponin-based Matrix-M adjuvant enhances the immune system response, making it broader and more durable.2 The Matrix-M adjuvant stimulates the entry of antigen-presenting cells at the injection site and enhances antigen presentation in local lymph nodes.

About Novavax
Novavax, Inc. (Nasdaq: NVAX) promotes improved health by discovering, developing and commercializing innovative vaccines to help protect against serious infectious diseases. Novavax, a global company based in Gaithersburg, Md., U.S., offers a differentiated vaccine platform that combines a recombinant protein approach, innovative nanoparticle technology and Novavax's patented Matrix-M adjuvant to enhance the immune response. The Company's portfolio includes its COVID-19 vaccine and its pipeline includes a vaccine for influenza and COVID-19 and influenza combined. In addition, Novavax's adjuvant is included in the University of Oxford and Serum Institute of India's R21/Matrix-M malaria vaccine. Please visit novavax.com and LinkedIn for more information. 

Forward-Looking Statements
Statements herein relating to the future of Novavax, its operating plans and prospects, the immunogenic response of its vaccine technology against variant strains and the scope, timing and outcome of future regulatory filings and actions, including the plan to be ready to deliver a JN.1 protein-based non-mRNA COVID-19 vaccine, and the extent of the availability of its vaccine at various locations, are forward-looking statements. Novavax cautions that these forward-looking statements are subject to numerous risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. These risks and uncertainties include, without limitation, antigenic drift or shift in the SARS-CoV2 spike protein, challenges satisfying, alone or together with partners, various safety, efficacy, and product characterization requirements, including those related to process qualification and assay validation, necessary to satisfy applicable regulatory authorities; difficulty obtaining scarce raw materials and supplies; resource constraints, including human capital and manufacturing capacity, on the ability of Novavax to pursue planned regulatory pathways; challenges or delays in obtaining regulatory authorization for its product candidates, including  an JN.1 protein-based non-mRNA COVID-19 vaccine or for future COVID-19 variant strain changes; challenges or delays in clinical trials; manufacturing, distribution or export delays or challenges; Novavax's exclusive dependence on Serum Institute of India Pvt. Ltd. for co-formulation and filling and the impact of any delays or disruptions in their operations on the delivery of customer orders; retail customer stocking strategies; warehouse order fulfilment execution, challenges meeting contractual requirements under agreements with multiple commercial, governmental, and other entities; and those other risk factors identified in the "Risk Factors" and "Management's Discussion and Analysis of Financial Condition and Results of Operations" sections of Novavax's Annual Report on Form 10-K for the year ended December 31, 2023, and subsequent Quarterly Reports on Form 10-Q, as filed with the Securities and Exchange Commission (SEC). We caution investors not to place considerable reliance on forward-looking statements contained in this press release. You are encouraged to read our filings with the SEC, available at www.sec.gov and www.novavax.com, for a discussion of these and other risks and uncertainties. The forward-looking statements in this press release speak only as of the date of this document, and we undertake no obligation to update or revise any of the statements. Our business is subject to substantial risks and uncertainties, including those referenced above. Investors, potential investors, and others should give careful consideration to these risks and uncertainties. 

Contacts:
Investors
Erika Schultz
240-268-2022
ir@novavax.com

Media
Giovanna Chandler
240-720-7804
media@novavax.com

References

  1. U.S. Centers for Disease Control and Prevention. Variant Proportions [Data set]. In COVID Data Tracker. 2024. Available at: https://covid.cdc.gov/covid-data-tracker/#variant-proportions
  2. Stertman L, Palm AE, Zarnegar B, et al. The Matrix-M™ adjuvant: A critical component of vaccines for the 21st century. Hum Vaccin Immunother. 2023;19(1):2189885. doi:10.1080/21645515.2023.2189885.

 

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/novavax-2024-2025-formula-covid-19-vaccine-available-at-major-pharmacies-across-the-us-302247738.html

SOURCE Novavax, Inc.

FAQ

When was Novavax's 2024-2025 Formula COVID-19 Vaccine authorized by the FDA?

The FDA authorized Novavax's 2024-2025 Formula COVID-19 Vaccine under Emergency Use Authorization (EUA) on August 30, 2024.

What age group is eligible for Novavax's 2024-2025 COVID-19 Vaccine?

Novavax's 2024-2025 COVID-19 Vaccine is authorized for individuals aged 12 and older.

Where can I find Novavax’s 2024-2025 COVID-19 Vaccine?

The vaccine is available at major pharmacy retailers like CVS, Rite Aid, Walgreens, Costco, and many others.

What are the common side effects of Novavax’s 2024-2025 COVID-19 Vaccine?

Common side effects include injection site pain, fatigue, headaches, and muscle pain.

What strains does Novavax's 2024-2025 COVID-19 Vaccine target?

The vaccine targets the JN.1 strain and shows cross-reactivity with KP.2.3, KP.3, KP.3.1.1, and LB.1.1 strains.

What safety risks are associated with Novavax's 2024-2025 COVID-19 Vaccine?

The vaccine poses risks of myocarditis, pericarditis, and potential anaphylactic reactions.

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