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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

諾瓦瓦克斯醫藥向加拿大衛生部提交了新的基於蛋白質的2024-2025年新冠疫苗申請
諾瓦瓦克斯醫藥 ·  07/02 12:00
  • 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
  • 如果獲得授權,諾瓦瓦克斯的COVID-19生物-疫苗將是加拿大唯一的基於蛋白質的選擇。
  • 諾瓦瓦克斯的申報與NACI,美國FDA,EMA和WHO關於疫苗構成的建議一致。

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

美國馬里蘭州蓋瑟斯堡市,2024年7月2日/美通社/--全球貨幣推進基於蛋白質的疫苗的諾瓦瓦克斯公司(納斯達克:NVAX)Matrix-M佐劑。宣佈已向加拿大衛生部提出授權NVX-CoV2705生物-疫苗(適用於12歲及以上人群)的申請。此提交遵循國家免疫顧問委員會(NACI)的指導,使用最新的選擇菌株,並遵循美國食品藥品監督管理局(FDA),歐洲藥品管理局(EMA)和世界衛生組織(WHO)的指導。美國食品藥品監督管理局(FDA)歐洲藥品管理局(EMA)和世界衛生組織和歐洲藥品管理局一致推薦並獲得VRBPAC今天的一致推薦,升級至 JN.1 系譜或 JN.1 可在今年秋季提供對 COVID-19 的保護所需。(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."

“諾瓦瓦克斯正在與加拿大衛生部密切合作,以在今年秋季爲所有符合條件的加拿大人批准更新的基於蛋白質的COVID-19疫苗選擇,”John C. Jacobs ,諾瓦瓦克斯總裁兼首席執行官說:“我們更新的COVID-19疫苗對JN.1,KP.2和KP.3都是有效的,另外還對其他JN.1亞譜系菌株也是有效的。”

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.

非臨床數據證明,諾瓦瓦克斯更新的COVID-19疫苗對包括F456L和R346T突變的JN.1 類病毒在內的廣泛中和反應、FLiRT變異株和KP.3等“FLuQE”變異株具有廣泛的中和反應。4-6諾瓦瓦克斯的疫苗還能產生對一系列JN.1系列變體的保守多功能、Th1偏向的CD4+ T細胞反應。4這些反應表明,諾瓦瓦克斯的疫苗技術對多個變異株具有廣譜中和反應,包括對循環前向漂移變異株的反應。

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.

諾瓦瓦克斯打算在獲得授權後立即在加拿大提供疫苗,如果公共衛生計劃選擇提供這種選擇。諾瓦瓦克斯已向醫藥監管部門提交了更新的COVID-19疫苗申請。美國食品和藥物管理局和頁面。EMA(European Medicines Agency)歐洲藥品管理局但也正在與全球的其他監管機構合作,以獲得其更新的COVID-19疫苗的授權或批准。

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.

關於Novavax COVID-19 2024-2025配方(NVX-CoV2705):
NVX-CoV2705是Novavax原型COVID-19疫苗(NVX-CoV2373)的升級版本,針對JN.1變體進行了制定。它是一種蛋白質疫苗,通過創建SARS-CoV-2表面削峯蛋白的副本來製造。Novavax獨特的重組納米粒子技術使得非傳染性削峯蛋白作爲抗原,使免疫系統能夠識別病毒,而Novavax的Matrix-M佐劑增強和擴展了免疫反應。該疫苗作爲一種現成的液體制劑包裝,存儲在2°到8°C之間,可以利用現有的疫苗供應和冷鏈渠道。

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.

關於Matrix-M佐劑:
當添加到疫苗中時,諾瓦瓦克斯的專利皁苷基Matrix-M佐劑增強了免疫系統的反應,使之更廣泛和更持久。Matrix-M佐劑刺激了注射部位的抗原遞呈細胞進入和局部淋巴結中的抗原遞呈。7全球貨幣(Nasdaq:NVAX)通過發現、開發和商業化創新疫苗的方式促進健康,幫助防止嚴重傳染性疾病。總部位於美國馬里蘭州蓋瑟斯堡市的諾瓦瓦克斯提供了一種不同於其他疫苗產品的疫苗平台,其中包括重組蛋白質方法、創新的納米顆粒技術和諾瓦瓦克斯的專利Matrix-M佐劑,以增強免疫反應。該公司的產品組合包括COVID-19疫苗和流感和COVID-19流感聯合疫苗。此外,諾瓦瓦克斯的佐劑被包括印度牛津大學和印度血清研究所的R21/Matrix-M瘧疾疫苗在內的其他疫苗中採用。

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.

關於諾瓦瓦克斯
這裏所述與諾瓦瓦克斯的未來、運營計劃和前景、其疫苗技術對變異株的免疫反應以及未來監管申報和行動(包括任何加拿大衛生部、EMA或FDA建議的)範圍、時間和結果等相關事宜的聲明屬於前瞻性聲明。諾瓦瓦克斯提醒這些前瞻性聲明受到許多風險和不確定性的影響,這些風險和不確定性可能導致實際結果與這些聲明所表達的結果有所不同。這些風險和不確定性包括但不限於SARS-CoV2尖峯蛋白抗原漂移或轉變,在提供符合應用法律法規的各種安全性、有效性和產品特徵要求(包括相關於工藝資格和測定驗證的要求),以及各種單獨或聯合滿足相關的監管機構要求的挑戰,可能存在的原材料和供應品稀缺困難,合作伙伴等方面的資源限制對諾瓦瓦克斯追求計劃中的監管途徑的影響,針對基於JN.1蛋白質的COVID-19疫苗或未來COVID-19變異株更改的監管授權或批准中的挑戰或延遲,臨床試驗中的挑戰或延遲,製造,分配或出口時的挑戰或延遲,以及Novavax 公司與 Serum Institute of India Pvt. Ltd. 的合作關係對於無配合和填充及他們經營對客戶訂單的交付的影響等等,以及上述列舉的其他風險因素在2023年12月31日的10-K年度報告以及隨後的10-Q季度報告中所列明的"風險因素"和"管理討論和分析財務狀況和業績"部分中有所指明。我們提醒投資者不要在此新聞稿中重大依賴前瞻性聲明。我們鼓勵您仔細閱讀我們在SEC提交的備案文件,可在www.sec.gov和www.novavax.com上獲取,以討論這些和其他風險和不確定性。本新聞稿中的前瞻性聲明僅準確無誤地反映了文檔發佈之日的情況,我們不承擔更新或修訂任何聲明的義務。我們的業務面臨着重大的風險和不確定性,包括上述引用的風險和不確定性。投資者、潛在投資者和其他人應認真考慮這些風險和不確定性。novavax.com和頁面。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.

前瞻性聲明
"更好的健康,全球貨幣(Nasdaq:NVAX)通過發現、開發和商業化創新疫苗的方式保護嚴重傳染性疾病的爆發。總部位於美國馬里蘭州蓋瑟斯堡市的諾瓦瓦克斯採用了一種與衆不同的疫苗平台,結合了一種重組蛋白質方法,一種創新的納米顆粒技術和諾瓦瓦克斯的專利基質M佐劑,以增強免疫反應。該公司的產品組合包括COVID-19疫苗和流感和COVID-19流感聯合疫苗。此外,諾瓦瓦克斯的配方葉苷基Matrix-M佐劑被印度牛津大學和印度血清研究所的R21/Matrix-M瘧疾疫苗採用。"

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

聯繫人:
投資者
Erika Schultz
240-268-2022
ir@諾瓦瓦克斯醫藥.com

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

媒體
喬萬娜·錢德勒
240-720-7804
media@諾瓦瓦克斯醫藥.com

References

參考

  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. 加拿大公共衛生機構NACI發佈指導方針,指導當2024年秋季使用COVID-19疫苗時。https://www.canada.ca/en/public-health/services/publications/vaccines-immunization/national-advisory-committee-immunization-guidance-covid-19-vaccines-fall-2024
  2. 美國食品藥品監督管理局。2024年秋季開始使用的更新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. 歐洲藥品管理局。etf建議更新covid-19疫苗以針對新的jn.1變種。2024年4月30日。網址:https://www.ema.europa.eu/en/news/etf-recommends-updating-covid-19-vaccines-target-new-jn1-variant
  4. 世界衛生組織。 COVID-19 疫苗抗原組成聲明。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. 美國疾病控制和預防中心。變種比例【數據集】。在 COVID 數據跟蹤器中。2024。可在:https://covid.cdc.gov/covid-data-tracker/#variant-proportions
  6. Focosi D, Spezia PG, Gueli F, Maggi F。FLips 時代:突刺蛋白 L455F 和 F456L(以及 A475V)如何塑造 SARS-CoV-2 進化。《病毒》。2023 年;16(1):3。2023 年 12 月 19 日發佈。DOI:10.3390/v16010003。病毒。2023年; 16 (1): 3。發佈於2023年12月19日。doi:10.3390/v16010003。
  7. Stertman L,Palm AE,Zarnegar B等。Matrix-M佐劑:21世紀疫苗的關鍵部分。Hum疫苗免疫療法。2023;19(1):2189885。doi:10.1080 / 21645515.2023.2189885。

譯文內容由第三人軟體翻譯。


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