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Press Release: New Beyfortus Data Featured at IDWeek Reinforce Real-world Effectiveness Against RSV Disease and Hospitalization in Infants

Press Release: New Beyfortus Data Featured at IDWeek Reinforce Real-world Effectiveness Against RSV Disease and Hospitalization in Infants

新聞發佈:IDWeek展示貝福特斯新數據,在嬰兒中抗擊RSV疾病和住院的實際有效性。
賽諾菲安萬特 ·  10/09 00:00

New Beyfortus data featured at IDWeek reinforce real-world effectiveness against RSV disease and hospitalization in infants

IDWeek上發佈的Beyfortus新數據增強了現實世界對抗呼吸道合胞病毒疾病和嬰兒住院的有效性

Paris, October 9, 2024. Sanofi advances its ambition to protect all infants from respiratory syncytial virus (RSV) disease with new Beyfortus (nirsevimab) data to be presented at the Infectious Disease Society of America's IDWeek 2024 annual meeting in Los Angeles, California, from October 16-19, 2024.

巴黎,2024 年 10 月 9 日。賽諾菲將在2024年10月16日至19日在加利福尼亞州洛杉磯舉行的美國傳染病學會2024年IDWeek年會上公佈貝福特斯(nirsevimab)的新數據,推進其保護所有嬰兒免受呼吸道合胞病毒(RSV)疾病侵害的雄心。

Thomas Triomphe
Executive Vice President, Vaccines, Sanofi
"The data featured at IDWeek from several national immunization programs will reinforce the proven efficacy and favorable safety profile of Beyfortus against RSV disease and hospitalization in infants. In just the first year of implementation, Beyfortus has demonstrated high real-world effectiveness consistently exceeding 80%. In addition, Beyfortus delivers this protection in the right dose for the right baby. We're proud to set a new standard with Beyfortus as the only approved and proven RSV protection for infants regardless of whether they are born before or during the RSV season, at term or preterm, healthy or with underlying conditions."

托馬斯·凱旋門
賽諾菲疫苗執行副總裁
「IDWeek上來自多個國家免疫計劃的數據將加強Beyfortus對抗呼吸道合胞病毒疾病和嬰兒住院治療的經過驗證的療效和良好的安全性。僅在實施的第一年,Beyfortus就表現出了持續超過80%的高實際效率。此外,Beyfortus 以正確的劑量爲合適的寶寶提供這種保護。我們很自豪能夠將Beyfortus作爲唯一獲得批准和驗證的嬰兒呼吸道合胞病毒保護的新標準,無論他們是在呼吸道合胞病毒季節之前還是出生期間、足月還是早產、健康還是有潛在疾病。」

Beyfortus doses continue to be shipped to meet global commitments ahead of the 2024-2025 RSV season. A second manufacturing filling line has been approved by regulatory authorities in the US, Canada, and Europe and represents the majority of our supply for the 2024-2025 season. A third filling line, expected to provide additional doses for the 2024-2025 season, is approved by the European Medicines Agency and under review by the US Food and Drug Administration.

在2024-2025年呼吸道合胞病毒季節之前,將繼續發貨Beyfortus劑量,以兌現全球承諾。第二條製造灌裝生產線已獲得美國、加拿大和歐洲監管機構的批准,佔我們2024-2025季節供應的大部分。第三條灌裝生產線已獲得歐洲藥品管理局的批准,並正在接受美國食品藥品監督管理局的審查,預計將爲2024-2025年季節提供額外劑量。

Beyfortus and RSV data at IDWeek 2024

2024 年 IDWeek 上的 Beyfortus 和 RSV 數據

  • Thursday, October 17, 12:15-1:30 pm PT: RSV Prophylaxis with Nirsevimab in Infants: Systematic Review of Early Real-World Evidence on Effectiveness and Impact (Sanofi, presented by Oliver Martyn, MPH, Poster# P-631)
  • Thursday, October 17, 12:15-1:30 pm PT: Implementation and Uptake of Nirsevimab within Nemours Children's Health Delaware Healthcare System (independent study by Nemours Children's Health Delaware, presented by Sara Mann, Poster# P-633)
  • Thursday, October 17, 1:15-2:00 pm PT Preventing RSV Lower Respiratory Tract Disease in Infants: The First Year in Review (Sanofi, Learning Lounge event)
  • Thursday, October 17, 1:45-3:00 pm PT: Universal Immunization Strategy Against Respiratory Syncytial Virus (RSV) Prevention in Chile with Nirsevimab during the 2024 Winter Season: First Southern Hemisphere Nationwide Effectiveness Data (independent study by University of Chile, presented by Juan Pablo Torres-Torretti, MD, PhD, during the Late Breaker Abstract Session: Respiratory Viruses Across All Ages, #169).
  • Friday, October 18, 12:15-1:30 pm PT: Significant Reduction in Disease Burden and a Shift in Clinical Diagnoses in Children Hospitalized with Respiratory Syncytial Virus (RSV) after Nirsevimab Implementation in Catalonia (Spain) (independent study presented by Anna Creus-Costa, MD, Poster# P-1186)
  • Friday, October 18, 12:15-1:30 pm PT: The burden of respiratory syncytial virus among Brazilian infants (BONSAI study): preliminary results (Sanofi, presented by Manoel Ribeiro, MD, PhD, Poster# P-1199)
  • Saturday, October 19, 12:15-1:30 pm PT: Nirsevimab in Patient Samples Does Not Interfere with Respiratory Syncytial Virus (RSV) Detection by Commercially Available Rapid Antigen Tests (AstraZeneca, presented by Sarah R. Sincero, BSc, Poster# P-2179)
  • 太平洋時間 10 月 17 日星期四下午 12:15-1:30:使用 Nirsevimab 預防嬰兒呼吸道合胞病毒:對早期現實世界中有效性和影響力證據的系統評價(賽諾菲,由公共衛生碩士 Oliver Martyn 主持,海報 # P-631)
  • 太平洋時間10月17日星期四下午 12:15-1:30:Nirsevimab在特拉華州內穆爾兒童健康醫療系統中的實施和使用(特拉華州內穆爾兒童健康中心的獨立研究,由薩拉·曼恩主持,海報# P-633)
  • 10月17日星期四下午 1:15-2:00 Pt 預防嬰兒呼吸道合胞病毒下呼吸道疾病:第一年回顧(賽諾菲,學習休息室活動)
  • 太平洋時間10月17日星期四下午 1:45-3:00:智利在2024年冬季使用Nirsevimab預防呼吸道合胞病毒(RSV)的全民免疫戰略:首份南半球全國有效性數據(智利大學的獨立研究,由醫學博士胡安·巴勃羅·託雷蒂博士在Late Breaker摘要會議:所有年齡段的呼吸道病毒,#169)。
  • 太平洋時間10月18日星期五下午 12:15-1:30:加泰羅尼亞(西班牙)實施Nirsevimab後,因呼吸道合胞病毒(RSV)住院的兒童的疾病負擔顯著減輕,臨床診斷髮生了變化(由醫學博士安娜·克魯斯-科斯塔發表的獨立研究,海報# P-1186)
  • 太平洋時間10月18日星期五下午 12:15-1:30:巴西嬰兒呼吸道合胞病毒的負擔(BONSAI 研究):初步結果(賽諾菲,由醫學博士、博士曼諾爾·裏貝羅主持,Poster# P-1199)
  • 太平洋時間 10 月 19 日星期六下午 12:15-1:30:患者樣本中的 Nirsevimab 不會干擾市售快速抗原檢測(阿斯利康,由莎拉·辛塞羅主持,理學學士,海報# P-2179)的呼吸道合胞病毒(RSV)檢測

About RSV
RSV is a highly contagious virus that can lead to serious respiratory illness for infants.1 Two out of three infants are infected with RSV during their first year of life and almost all children are infected by their second birthday.1,2 RSV is the most common cause of lower respiratory tract disease, including bronchiolitis and pneumonia, in infants.3 It is also a leading cause of hospitalization in infants worldwide, with most hospitalizations for RSV occurring in healthy infants born at term.4-7 Globally, in 2019, there were approximately 33 million cases of acute lower respiratory infections leading to more than 3 million hospitalizations in children younger than 5 years.8 RSV-related direct medical costs, globally — including hospital, outpatient and follow-up care — were estimated at €4.82 billion in 2017.9

關於 RSV
呼吸道合胞病毒是一種高度傳染性的病毒,可導致嬰兒出現嚴重的呼吸道疾病。1 三分之二的嬰兒在出生後的第一年就感染了呼吸道合胞病毒,幾乎所有兒童在第二個生日時都被感染。1,2 呼吸道合胞病毒是嬰兒下呼吸道疾病(包括毛細支氣管炎和肺炎)的最常見病因。3 它也是全球嬰兒住院的主要原因,大多數住院病例是呼吸道合胞病毒發生在妊娠期出生的健康嬰兒身上。4-7 2019年,全球約有3300萬急性病例下呼吸道感染導致超過300萬名5歲以下兒童住院。8 2017年,全球與RSV相關的直接醫療費用,包括住院、門診和後續護理,估計爲48.2歐元。9

About Beyfortus
Beyfortus (nirsevimab) is the first immunization designed for all infants for protection against RSV disease through their first RSV season, including for those born healthy at term or preterm, or with specific health conditions. Beyfortus is also designed to protect children up to 24 months of age who remain vulnerable to severe RSV disease through their second RSV season.

關於 Beyfortus
Beyfortus(nirsevimab)是第一款專爲所有嬰兒設計的免疫接種,旨在在第一個呼吸道合胞病毒季節預防呼吸道合胞病毒疾病,包括那些在足月或早產時出生時健康或有特定健康狀況的嬰兒。Beyfortus還旨在保護24個月以下在第二個呼吸道合胞病毒季節期間仍然容易感染嚴重呼吸道合胞病毒疾病的兒童。

As a long-acting antibody provided directly to newborns and infants as a single dose, Beyfortus offers rapid protection to help prevent lower respiratory tract disease caused by RSV without requiring activation of the immune system. Beyfortus administration can be timed to coincide with the RSV season.

作爲一種以單劑量直接提供給新生兒和嬰兒的長效抗體,Beyfortus 提供快速保護,無需激活免疫系統即可幫助預防由呼吸道合胞病毒引起的下呼吸道疾病。Beyfortus的管理時間可以與呼吸道合胞病毒季節相吻合。

Beyfortus has been approved for use in the European Union, the US, China, Japan, and many other countries around the world. Special designations to facilitate expedited development of Beyfortus were granted by several regulatory agencies, including Breakthrough Therapy Designation and Priority Review designation by The China Center for Drug Evaluation under the National Medical Products Administration; Breakthrough Therapy Designation and Fast Track Designation from the US Food and Drug Administration; access granted to the European Medicines Agency (EMA) PRIority MEdicines (PRIME) scheme and EMA accelerated assessment; Promising Innovative Medicine designation by the UK Medicines and Healthcare products Regulatory Agency; and Beyfortus has been named "a medicine for prioritized development" under the Project for Drug Selection to Promote New Drug Development in Pediatrics by the Japan Agency for Medical Research and Development.

Beyfortus 已獲准在歐盟、美國、中國、日本和世界上許多其他國家使用。多個監管機構批准了促進Beyfortus加速開發的特別稱號,包括國家藥品監督管理局中國藥物評估中心頒發的突破性療法指定和優先審評指定;美國食品藥品監督管理局的突破性療法認證和快速通道認定;歐洲藥品管理局(EMA)優先藥物(PRIME)計劃和EMA加速評估的准入;英國藥品監督管理局的有前途的創新藥物認證;以及在日本醫學研究開發署促進兒科新藥開發的藥物篩選項目下,醫療保健產品監管局和Beyfortus被評爲 「優先開發藥物」。

About Sanofi
We are an innovative global healthcare company, driven by one purpose: we chase the miracles of science to improve people's lives. Our team, across the world, is dedicated to transforming the practice of medicine by working to turn the impossible into the possible. We provide potentially life-changing treatment options and life-saving vaccine protection to millions of people globally, while putting sustainability and social responsibility at the center of our ambitions.

關於賽諾菲
我們是一家創新的全球醫療保健公司,我們的目標只有一個:我們追逐科學奇蹟以改善人們的生活。我們的團隊遍佈世界各地,致力於將不可能變爲可能,從而改變醫學實踐。我們爲全球數百萬人提供可能改變生活的治療選擇和挽救生命的疫苗保護,同時將可持續發展和社會責任置於我們雄心壯志的中心。

Sanofi is listed on EURONEXT: SAN and NASDAQ: SNY

賽諾菲在泛歐交易所:SAN 和納斯達克上市:SNY

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賽諾菲前瞻性陳述
本新聞稿包含經修訂的1995年《私人證券訴訟改革法》中定義的前瞻性陳述。前瞻性陳述是不是歷史事實的陳述。這些陳述包括對產品營銷和其他潛力的預測和估計,或對該產品未來潛在收入的預測和估計。前瞻性陳述通常由 「期望」、「預期」、「相信」、「打算」、「估計」、「計劃」 和類似表述來識別。儘管賽諾菲管理層認爲此類前瞻性陳述中反映的預期是合理的,但提醒投資者,前瞻性信息和陳述存在各種風險和不確定性,其中許多風險和不確定性難以預測,通常超出賽諾菲的控制範圍,這可能導致實際業績和發展與前瞻性信息和陳述所表達、暗示或預測的業績和發展存在重大差異。除其他外,這些風險和不確定性包括可能影響產品可用性或商業潛力的意外監管行動或延誤,或一般的政府監管、產品可能無法在商業上取得成功的事實、研發中固有的不確定性,包括未來的臨床數據和對與產品相關的現有臨床數據的分析,包括上市後、意外安全、質量或製造問題、總體競爭、與知識產權相關的風險以及任何相關的未來訴訟和此類訴訟的最終結果,動盪的經濟和市場狀況,以及疫情或其他全球危機可能對我們、我們的客戶、供應商、供應商和其他商業夥伴以及其中任何一方的財務狀況以及我們的員工和整個全球經濟產生的影響。風險和不確定性還包括賽諾菲在向美國證券交易委員會和AMF提交的公開文件中討論或確定的不確定性,包括賽諾菲截至2023年12月31日止年度的20-F表年度報告中 「風險因素」 和 「關於前瞻性陳述的警示性聲明」 中列出的不確定性。除適用法律的要求外,賽諾菲不承擔任何更新或修改任何前瞻性信息或陳述的義務。

All trademarks mentioned in this press release are the property of the Sanofi group.

本新聞稿中提及的所有商標均爲賽諾菲集團的財產。

References:

參考文獻:

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