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Moderna Announces First Participant Dosed in Pivotal Phase 3 Trial of Investigational MRNA Norovirus Vaccine, MRNA-1403

Moderna Announces First Participant Dosed in Pivotal Phase 3 Trial of Investigational MRNA Norovirus Vaccine, MRNA-1403

moderna宣佈其實驗性mRNA諾如病毒疫苗MRNA-1403關鍵第3階段試驗中第一位接受試驗者已接種
Accesswire ·  09/30 19:00

CAMBRIDGE, MA / ACCESSWIRE / September 30, 2024 / Moderna, Inc. (NASDAQ:MRNA) today announced that the first participant in the U.S. has been dosed in the Nova 301 Trial, a pivotal Phase 3 randomized clinical trial evaluating the efficacy, safety, and immunogenicity of an investigational norovirus vaccine, mRNA-1403. Global recruitment for the Nova 301 trial has also begun.

劍橋,MA / ACCESSWIRE / 2024年9月30日 / Moderna公司(納斯達克:moderna)今天宣佈,在美國首位參與者接受了Nova 301試驗的劑量,這是一項關鍵的III期隨機臨床試驗,評估了一種非羅病毒調查性疫苗mRNA-1403的效力、安全性和免疫原性。Nova 301試驗的全球招募也已經開始。

"Norovirus is a significant public health concern that affects millions of people worldwide each year, leading to severe symptoms and, in some cases, hospitalization," said Stéphane Bancel, CEO of Moderna. "By advancing our investigational norovirus vaccine into a pivotal Phase 3 trial, we are one step closer to potentially providing a new tool to prevent infection from this highly contagious virus, which places a significant burden on health systems globally."

「羅病毒是一個重要的公共衛生問題,每年影響全球數百萬人,導致嚴重症狀,並在某些情況下導致住院,」 Moderna首席執行官斯蒂凡•班瑟爾表示。「通過將我們的調查性羅病毒疫苗推進至關鍵的III期試驗,我們離潛在提供新工具預防這種極具傳染性病毒感染的目標更近一步,這正在全球衛生系統上造成重大負擔。」

The Nova 301 Phase 3 trial is a randomized, observer-blind, placebo-controlled trial evaluating the efficacy, safety and immunogenicity of mRNA-1403. The trial aims to enroll approximately 25,000 participants 18 years of age and older globally, including in countries in the Northern Hemisphere (U.S., Canada, UK, Japan), the equatorial region, and the Southern Hemisphere (Australia and countries in South America). Approximately 20,000 participants 60 years of age and older and 5,000 participants between 18 and 59 years of age will be enrolled to assess the investigational vaccine's ability to protect against moderate to severe norovirus acute gastroenteritis (AGE) in adults, with a focus on the older age group that is at greatest risk of severe outcomes including hospitalization.

Nova 301第III期試驗是一項隨機、觀察者盲法、安慰劑對照的試驗,評估了mRNA-1403的效力、安全性和免疫原性。該試驗旨在全球範圍內招募約25,000名18歲及以上的參與者,包括北半球國家(美國、加拿大、英國、日本)、赤道地區和南半球國家(澳大利亞和南美洲國家)。約20,000名60歲及以上的參與者和5,000名18至59歲的參與者將被招募,以評估調查性疫苗在預防成年人中輕到重度羅病毒急性胃腸炎(AGE)中的能力,重點關注那些處於重症結果(包括住院)最高風險的老年人群。

Enteric viruses, including norovirus, are a leading cause of diarrheal diseases, resulting in significant morbidity and mortality worldwide, particularly among young children and older adults. Norovirus is highly contagious and a leading cause of diarrheal disease globally, associated with 18% of all AGE,1 resulting in approximately 200,000 deaths per year and substantial healthcare costs.2

腸道病毒,包括羅病毒,是導致腹瀉疾病的主要原因,世界範圍內引起顯着的發病率和死亡率,尤其是在幼兒和老年人群中。羅病毒具有極強的傳染性,在全球是引起腹瀉疾病的主要原因之一,與所有AGE的18%有關,導致每年約20萬人死亡,且醫療保健成本極高。

mRNA-1403 is an mRNA vaccine in development to prevent moderate to severe acute gastroenteritis caused by norovirus. The vaccine candidate is a trivalent formulation containing mRNA that encodes for virus-like particles (VLPs) designed to protect against multiple norovirus genotypes.

mRNA-1403是一種mRNA生物-疫苗,旨在預防因諾如病毒引起的中至重度急性胃腸炎。這種疫苗候選者是一種三價配方,含有編碼病毒樣顆粒(VLPs)的mRNA,旨在保護免受多種諾如病毒基因型的侵害。

About Moderna

關於現代

Moderna is a leader in the creation of the field of mRNA medicine. Through the advancement of mRNA technology, Moderna is reimagining how medicines are made and transforming how we treat and prevent disease for everyone. By working at the intersection of science, technology and health for more than a decade, the company has developed medicines at unprecedented speed and efficiency, including one of the earliest and most effective COVID-19 vaccines.

Moderna是mRNA醫學領域的領軍者。通過推動mRNA技術的進步,現代正在重新構想藥物的製造方式,爲所有人治療和預防疾病。通過在科學、技術和健康交叉領域工作十多年,公司已以前所未有的速度和效率開發出藥物,包括最早和最有效的COVID-19疫苗之一。

Moderna's mRNA platform has enabled the development of therapeutics and vaccines for infectious diseases, immuno-oncology, rare diseases and autoimmune diseases. With a unique culture and a global team driven by the Moderna values and mindsets to responsibly change the future of human health, Moderna strives to deliver the greatest possible impact to people through mRNA medicines. For more information about Moderna, please visit modernatx.com and connect with us on X (formerly Twitter), Facebook, Instagram, YouTube and LinkedIn.

Moderna的mRNA平台使得感染性疾病、免疫治療、罕見病和自身免疫性疾病的治療和疫苗的開發成爲可能。Moderna擁有獨特的文化和全球團隊,秉持Moderna價值觀和思維方式,爲了負責任地改變人們未來的健康而努力,致力於通過mRNA藥物帶來最大的影響。有關Moderna的更多信息,請訪問modernatx.com,並在X(原Twitter)、Facebook、Instagram、YouTube和LinkedIn上與我們聯繫。

Forward-Looking Statements

前瞻性聲明

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including statements regarding: the potential for mRNA-1403 to prevent infection from norovirus; and anticipated enrollment in the Nova 301 Phase 3 trial. The forward-looking statements in this press release are neither promises nor guarantees, and you should not place undue reliance on these forward-looking statements because they involve known and unknown risks, uncertainties, and other factors, many of which are beyond Moderna's control and which could cause actual results to differ materially from those expressed or implied by these forward-looking statements. These risks, uncertainties, and other factors include, among others, those risks and uncertainties described under the heading "Risk Factors" in Moderna's Annual Report on Form 10-K for the fiscal year ended December 31, 2023, and in subsequent filings made by Moderna with the U.S. Securities and Exchange Commission, which are available on the SEC's website at www.sec.gov. Except as required by law, Moderna disclaims any intention or responsibility for updating or revising any forward-looking statements contained in this press release in the event of new information, future developments or otherwise. These forward-looking statements are based on Moderna's current expectations and speak only as of the date of this press release.

本新聞稿包含根據1995年修訂版《私人證券訴訟改革法》(Private Securities Litigation Reform Act of 1995)發表的前瞻性聲明,包括有關 mRNA-1403 可能預防諾如病毒感染的潛力;以及 Nova 301 第三階段試驗預期招募情況的聲明。本新聞稿中的前瞻性聲明既不承諾也不保證,您不應過分依賴這些前瞻性聲明,因爲它們涉及已知和未知的風險、不確定因素和其他因素,其中許多超出 moderna 的控制範圍,可能導致實際結果與這些前瞻性聲明所暗示或表達的有重大差異。這些風險、不確定因素和其他因素包括但不限於,Moderna在截至2023年12月31日的財政年度10-K表格中描述的《風險因素》中所描述的那些風險和不確定因素,以及 Moderna向美國證券交易委員會提交的後續文件,可在SEC的網站 www.sec.gov 上查閱。除非法律要求,Moderna 不對根據新信息、未來發展或其他情況更新或修訂本新聞稿中包含的任何前瞻性聲明而負責。這些前瞻性聲明基於 Moderna 目前的期望,並僅於本新聞稿發佈日期起有效。

Moderna Contacts

現代聯繫人

Media:
Luke Mircea-Willats
Senior Director, International Communications
Luke.mirceawillats@modernatx.com

媒體:
Luke Mircea-Willats
高級主任,國際通訊
Luke.mirceawillats@modernatx.com

Investors:
Lavina Talukdar
Senior Vice President & Head of Investor Relations
+1 617-209-5834
Lavina.Talukdar@modernatx.com

投資者:
Lavina Talukdar
高級副主席,投資者關係負責人
+1 617-209-5834
Lavina.Talukdar@modernatx.com

1 Ahmed, S.M., et al., Global prevalence of norovirus in cases of gastroenteritis: a systematic review and meta-analysis. Lancet Infect Dis, 2014
2

Ahmed等人發表的《關於胃腸炎諾如病毒的全球流行病學:系統性綜述和薈萃分析》發表在2014年《柳葉刀傳染病》期刊上
2

SOURCE: Moderna, Inc.

來源:現代RNA股份有限公司。

譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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