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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宣布第一个接受试验的重要第三阶段测试,即疫苗生物-疫苗MRNA诺如病毒疫苗MRNA-1403。
Accesswire ·  09/30 07:00

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.

马萨诸塞州剑桥市/ACCESSWIRE/2024年9月30日/Moderna, Inc.(纳斯达克股票代码:MRNA)今天宣布,Nova 301试验是评估在研诺如病毒疫苗mRNA-1403的疗效、安全性和免疫原性的关键性3期随机临床试验,美国的第一位参与者服用了剂量。Nova 301试验的全球招募工作也已开始。

"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."

Moderna首席执行官斯特凡·班塞尔说:“诺如病毒是一个重大的公共卫生问题,每年影响全球数百万人,导致严重症状,在某些情况下还会住院。”“通过将我们的研究型诺如病毒疫苗推进到一项关键的三期试验,我们离可能提供一种预防这种高度传染性病毒感染的新工具又近了一步,这种病毒给全球卫生系统带来了沉重负担。”

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 3期试验是一项随机、观察者失明、安慰剂对照的试验,旨在评估mRNA-1403的疗效、安全性和免疫原性。该试验旨在在全球范围内招收约25,000名18岁及以上的参与者,包括北半球(美国、加拿大、英国、日本)、赤道地区和南半球(澳大利亚和南美国家)的国家。将招募约20,000名60岁及以上的参与者和5,000名年龄在18至59岁之间的参与者,以评估该研究疫苗对成人中度至重度诺如病毒急性胃肠炎(AGE)的预防能力,重点是发生包括住院在内的严重结局风险最大的年龄组。

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

肠道病毒,包括诺如病毒,是腹泻疾病的主要病因,导致全球发病率和死亡率很高,在幼儿和老年人中尤其如此。诺如病毒具有高度传染性,是全球腹泻病的主要病因,占所有年龄段的18%1,每年导致约20万人死亡,医疗费用巨大。2

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 是一种正在开发的 mRNA 疫苗,用于预防由诺如病毒引起的中度至重度急性胃肠炎。候选疫苗是一种含有mRNA的三价配方,可编码病毒样颗粒(VLP),旨在抵御多种诺如病毒基因型。

About Moderna

关于 Moderna

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 是创建 mRNA 医学领域的领导者。通过mRNA技术的进步,Moderna正在重新构想药物的制造方式,并改变我们为所有人治疗和预防疾病的方式。通过在科学、技术和健康的交汇处工作了十多年,该公司以前所未有的速度和效率开发了药物,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 平台使传染病、免疫肿瘤学、罕见病和自身免疫性疾病的疗法和疫苗的开发成为可能。凭借独特的文化和以 Moderna 价值观和心态为驱动的全球团队,负责任地改变人类健康的未来,Moderna 致力于通过 mRNA 药物为人们带来尽可能大的影响。要了解有关 Moderna 的更多信息,请访问 modernatx.com 并通过 X(前身为 Twitter)、Facebook、Instagram、YouTube 和 LinkedIn 联系我们。

Forward-Looking Statements

前瞻性陈述

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.

本新闻稿包含经修订的1995年《私人证券诉讼改革法》所指的前瞻性陈述,包括有关以下内容的声明:mRNA-1403预防诺如病毒感染的可能性;以及Nova 301第三阶段试验的预期注册人数。本新闻稿中的前瞻性陈述既不是承诺也不是保证,您不应过分依赖这些前瞻性陈述,因为它们涉及已知和未知的风险、不确定性和其他因素,其中许多因素超出了Moderna的控制范围,可能导致实际结果与这些前瞻性陈述所表达或暗示的结果存在重大差异。这些风险、不确定性和其他因素包括Moderna截至2023年12月31日财年的10-k表年度报告以及Moderna随后向美国证券交易委员会提交的文件(可在美国证券交易委员会网站www.sec.gov上查阅)中 “风险因素” 标题下描述的风险和不确定性。除非法律要求,否则,如果出现新信息、未来发展或其他情况,Moderna不打算或承担任何更新或修改本新闻稿中包含的任何前瞻性陈述的意图或责任。这些前瞻性陈述基于Moderna当前的预期,仅代表截至本新闻稿发布之日。

Moderna Contacts

摩德纳联系人

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

媒体:
卢克·米尔恰-威拉茨
国际传播高级董事
Luke.mirceawillats@modernatx.com

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

投资者:
拉维娜·塔鲁克达尔
高级副总裁兼投资者关系主管
+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

1 Ahmed,S.m. 等人,胃肠炎病例中诺如病毒的全球流行率:系统评价和荟萃分析。《柳叶刀感染症》,2014
2

SOURCE: Moderna, Inc.

资料来源:Moderna, Inc.

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