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Novavax Submits Application to Health Canada for Updated Protein-based 2024-2025 Formula COVID-19 Vaccine

Novavax Submits Application to Health Canada for Updated Protein-based 2024-2025 Formula COVID-19 Vaccine

诺瓦瓦克斯医药向加拿大卫生部提交了新的基于蛋白质的2024-2025年新冠疫苗申请
诺瓦瓦克斯医药 ·  07/02 00:00
  • Novavax's COVID-19 vaccine would be the only protein-based option available in Canada, if authorized
  • Novavax's filing is aligned with NACI, U.S. FDA, EMA and WHO recommendations on vaccine composition
  • 如果获得授权,诺瓦瓦克斯的COVID-19生物-疫苗将是加拿大唯一的基于蛋白质的选择。
  • 诺瓦瓦克斯的申报与NACI,美国FDA,EMA和WHO关于疫苗构成的建议一致。

GAITHERSBURG, Md., July 2, 2024 /PRNewswire/ -- Novavax, Inc. (Nasdaq: NVAX), a global company advancing protein-based vaccines with its Matrix-M adjuvant, announced that it has filed for authorization with Health Canada for its 2024-2025 Formula COVID-19 vaccine (NVX-CoV2705) for individuals aged 12 and older. The submission follows the National Advisory Committee on Immunization (NACI) guidance to use the latest selected strain and the guidance from the U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA) and World Health Organization (WHO).1-4

美国马里兰州盖瑟斯堡市,2024年7月2日/美通社/--全球货币推进基于蛋白质的疫苗的诺瓦瓦克斯公司(纳斯达克:NVAX)Matrix-M佐剂。宣布已向加拿大卫生部提出授权NVX-CoV2705生物-疫苗(适用于12岁及以上人群)的申请。此提交遵循国家免疫顾问委员会(NACI)的指导,使用最新的选择菌株,并遵循美国食品药品监督管理局(FDA),欧洲药品管理局(EMA)和世界卫生组织(WHO)的指导。美国食品药品监督管理局(FDA)欧洲药品管理局(EMA)和世界卫生组织和欧洲药品管理局一致推荐并获得VRBPAC今天的一致推荐,升级至 JN.1 系谱或 JN.1 可在今年秋季提供对 COVID-19 的保护所需。(WHO)。1-4

"Novavax is working closely with Health Canada to have an updated protein-based COVID-19 vaccine option approved for all eligible Canadians this fall," said John C. Jacobs, President and Chief Executive Officer, Novavax. "Our updated COVID-19 vaccine is active against JN.1, KP.2 and KP.3, in addition to other JN.1 sublineage strains."

“诺瓦瓦克斯正在与加拿大卫生部密切合作,以在今年秋季为所有符合条件的加拿大人批准更新的基于蛋白质的COVID-19疫苗选择,”John C. Jacobs ,诺瓦瓦克斯总裁兼首席执行官说:“我们更新的COVID-19疫苗对JN.1,KP.2和KP.3都是有效的,另外还对其他JN.1亚谱系菌株也是有效的。”

Nonclinical data have demonstrated that Novavax's updated COVID-19 vaccine induces broad neutralization responses to JN.1 lineage viruses, including those containing the F456L and R346T mutations, to "FLiRT" variants and to "FLuQE" variants such as KP.3.4-6 Novavax's vaccine also produces conserved polyfunctional, Th1-biased CD4+ T cell responses to a wide range of JN.1 lineage variants.4 These responses indicate that Novavax's vaccine technology induces broadly neutralizing responses against multiple variant strains, including responses to circulating forward drift variants.

非临床数据证明,诺瓦瓦克斯更新的COVID-19疫苗对包括F456L和R346T突变的JN.1 类病毒在内的广泛中和反应、FLiRT变异株和KP.3等“FLuQE”变异株具有广泛的中和反应。4-6诺瓦瓦克斯的疫苗还能产生对一系列JN.1系列变体的保守多功能、Th1偏向的CD4+ T细胞反应。4这些反应表明,诺瓦瓦克斯的疫苗技术对多个变异株具有广谱中和反应,包括对循环前向漂移变异株的反应。

Novavax intends to have its vaccine available in Canada for immediate release post-authorization, should public health programs choose to provide this option. Novavax has filed with the U.S. FDA and EMA, and is working with other regulatory authorities globally on authorization or approval of its updated COVID-19 vaccine.

诺瓦瓦克斯打算在获得授权后立即在加拿大提供疫苗,如果公共卫生计划选择提供这种选择。诺瓦瓦克斯已向医药监管部门提交了更新的COVID-19疫苗申请。美国食品和药物管理局和页面。EMA(European Medicines Agency)欧洲药品管理局但也正在与全球的其他监管机构合作,以获得其更新的COVID-19疫苗的授权或批准。

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.

关于Novavax COVID-19 2024-2025配方(NVX-CoV2705):
NVX-CoV2705是Novavax原型COVID-19疫苗(NVX-CoV2373)的升级版本,针对JN.1变体进行了制定。它是一种蛋白质疫苗,通过创建SARS-CoV-2表面削峰蛋白的副本来制造。Novavax独特的重组纳米粒子技术使得非传染性削峰蛋白作为抗原,使免疫系统能够识别病毒,而Novavax的Matrix-M佐剂增强和扩展了免疫反应。该疫苗作为一种现成的液体制剂包装,存储在2°到8°C之间,可以利用现有的疫苗供应和冷链渠道。

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.7 The Matrix-M adjuvant stimulates the entry of antigen-presenting cells at the injection site and enhances antigen presentation in local lymph nodes.

关于Matrix-M佐剂:
当添加到疫苗中时,诺瓦瓦克斯的专利皂苷基Matrix-M佐剂增强了免疫系统的反应,使之更广泛和更持久。Matrix-M佐剂刺激了注射部位的抗原递呈细胞进入和局部淋巴结中的抗原递呈。7全球货币(Nasdaq:NVAX)通过发现、开发和商业化创新疫苗的方式促进健康,帮助防止严重传染性疾病。总部位于美国马里兰州盖瑟斯堡市的诺瓦瓦克斯提供了一种不同于其他疫苗产品的疫苗平台,其中包括重组蛋白质方法、创新的纳米颗粒技术和诺瓦瓦克斯的专利Matrix-M佐剂,以增强免疫反应。该公司的产品组合包括COVID-19疫苗和流感和COVID-19流感联合疫苗。此外,诺瓦瓦克斯的佐剂被包括印度牛津大学和印度血清研究所的R21/Matrix-M疟疾疫苗在内的其他疫苗中采用。

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.

关于诺瓦瓦克斯
这里所述与诺瓦瓦克斯的未来、运营计划和前景、其疫苗技术对变异株的免疫反应以及未来监管申报和行动(包括任何加拿大卫生部、EMA或FDA建议的)范围、时间和结果等相关事宜的声明属于前瞻性声明。诺瓦瓦克斯提醒这些前瞻性声明受到许多风险和不确定性的影响,这些风险和不确定性可能导致实际结果与这些声明所表达的结果有所不同。这些风险和不确定性包括但不限于SARS-CoV2尖峰蛋白抗原漂移或转变,在提供符合应用法律法规的各种安全性、有效性和产品特征要求(包括相关于工艺资格和测定验证的要求),以及各种单独或联合满足相关的监管机构要求的挑战,可能存在的原材料和供应品稀缺困难,合作伙伴等方面的资源限制对诺瓦瓦克斯追求计划中的监管途径的影响,针对基于JN.1蛋白质的COVID-19疫苗或未来COVID-19变异株更改的监管授权或批准中的挑战或延迟,临床试验中的挑战或延迟,制造,分配或出口时的挑战或延迟,以及Novavax 公司与 Serum Institute of India Pvt. Ltd. 的合作关系对于无配合和填充及他们经营对客户订单的交付的影响等等,以及上述列举的其他风险因素在2023年12月31日的10-K年度报告以及随后的10-Q季度报告中所列明的"风险因素"和"管理讨论和分析财务状况和业绩"部分中有所指明。我们提醒投资者不要在此新闻稿中重大依赖前瞻性声明。我们鼓励您仔细阅读我们在SEC提交的备案文件,可在www.sec.gov和www.novavax.com上获取,以讨论这些和其他风险和不确定性。本新闻稿中的前瞻性声明仅准确无误地反映了文档发布之日的情况,我们不承担更新或修订任何声明的义务。我们的业务面临着重大的风险和不确定性,包括上述引用的风险和不确定性。投资者、潜在投资者和其他人应认真考虑这些风险和不确定性。novavax.com和页面。LinkedIn了解更多信息。

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 any Health Canada, EMA or FDA recommendations, the timing of its delivery for a JN.1 protein-based COVID-19 vaccine this fall, 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 a JN.1 protein-based 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; 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.

前瞻性声明
"更好的健康,全球货币(Nasdaq:NVAX)通过发现、开发和商业化创新疫苗的方式保护严重传染性疾病的爆发。总部位于美国马里兰州盖瑟斯堡市的诺瓦瓦克斯采用了一种与众不同的疫苗平台,结合了一种重组蛋白质方法,一种创新的纳米颗粒技术和诺瓦瓦克斯的专利基质M佐剂,以增强免疫反应。该公司的产品组合包括COVID-19疫苗和流感和COVID-19流感联合疫苗。此外,诺瓦瓦克斯的配方叶苷基Matrix-M佐剂被印度牛津大学和印度血清研究所的R21/Matrix-M疟疾疫苗采用。"

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

联系人:
投资者
Erika Schultz
240-268-2022
ir@诺瓦瓦克斯医药.com

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

媒体
乔万娜·钱德勒
240-720-7804
media@诺瓦瓦克斯医药.com

References

参考

  1. Public Health Agency of Canada. Guidance on the use of COVID-19 vaccines during the fall of 2024. May 5, 2024. Available at: https://www.canada.ca/en/public-health/services/publications/vaccines-immunization/national-advisory-committee-immunization-guidance-covid-19-vaccines-fall-2024
  2. U.S. Food and Drug Administration. Updated COVID-19 Vaccines for Use in the United States Beginning in Fall 2024. June 13, 2024. Available at: https://www.fda.gov/vaccines-blood-biologics/updated-covid-19-vaccines-use-united-states-beginning-fall-2024
  3. European Medicines Agency. ETF recommends updating COVID-19 vaccines to target new JN.1 variant. April 30, 2024. Available at: https://www.ema.europa.eu/en/news/etf-recommends-updating-covid-19-vaccines-target-new-jn1-variant
  4. World Health Organization. Statement on the antigen composition of COVID-19 vaccines. April 26, 2024. Available at: https://www.who.int/news/item/26-04-2024-statement-on-the-antigen-composition-of-covid-19-vaccines
  5. 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
  6. Focosi D, Spezia PG, Gueli F, Maggi F. The Era of the FLips: How Spike Mutations L455F and F456L (and A475V) Are Shaping SARS-CoV-2 Evolution. Viruses. 2023;16(1):3. Published 2023 Dec 19. doi:10.3390/v16010003.
  7. 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.
  1. 加拿大公共卫生机构NACI发布指导方针,指导当2024年秋季使用COVID-19疫苗时。https://www.canada.ca/en/public-health/services/publications/vaccines-immunization/national-advisory-committee-immunization-guidance-covid-19-vaccines-fall-2024
  2. 美国食品药品监督管理局。2024年秋季开始使用的更新COVID-19疫苗。2024年6月13日。在: https://www.fda.gov/vaccines-blood-biologics/updated-covid-19-vaccines-use-united-states-beginning-fall-2024
  3. 欧洲药品管理局。etf建议更新covid-19疫苗以针对新的jn.1变种。2024年4月30日。网址:https://www.ema.europa.eu/en/news/etf-recommends-updating-covid-19-vaccines-target-new-jn1-variant
  4. 世界卫生组织。 COVID-19 疫苗抗原组成声明。2024 年4月26日。可在:https://www.who.int/news/item/26-04-2024-statement-on-the-antigen-composition-of-covid-19-vaccines
  5. 美国疾病控制和预防中心。变种比例【数据集】。在 COVID 数据跟踪器中。2024。可在:https://covid.cdc.gov/covid-data-tracker/#variant-proportions
  6. Focosi D, Spezia PG, Gueli F, Maggi F。FLips 时代:突刺蛋白 L455F 和 F456L(以及 A475V)如何塑造 SARS-CoV-2 进化。《病毒》。2023 年;16(1):3。2023 年 12 月 19 日发布。DOI:10.3390/v16010003。病毒。2023年; 16 (1): 3。发布于2023年12月19日。doi:10.3390/v16010003。
  7. Stertman L,Palm AE,Zarnegar B等。Matrix-M佐剂:21世纪疫苗的关键部分。Hum疫苗免疫疗法。2023;19(1):2189885。doi:10.1080 / 21645515.2023.2189885。
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