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Emergent BioSolutions Announces Initiation of Phase 1 Study Evaluating Its Universal Influenza Vaccine Candidate

Emergent BioSolutions Announces Initiation of Phase 1 Study Evaluating Its Universal Influenza Vaccine Candidate

Emerent BioSolutions公司宣佈啟動第一階段研究,評估其通用流感候選疫苗
GlobeNewswire ·  2021/12/16 21:57

GAITHERSBURG, Md., Dec. 16, 2021 (GLOBE NEWSWIRE) -- Emergent BioSolutions Inc. (NYSE: EBS) today announced the first participant dosed in its phase 1 study, EBS-UFV-001, evaluating the safety, tolerability, and immunogenicity of the company's investigational universal influenza vaccine candidate. This current version of Emergent's universal influenza vaccine candidate contains multiple components intended to induce broad and supra-seasonal immunity against influenza A viruses.

亞洲網馬裏蘭州蓋瑟斯堡2021年12月16日電Emergent BioSolutions Inc.(紐約證券交易所市場代碼:EBS)今天宣佈,該公司正在研究的通用流感候選疫苗的安全性、耐受性和免疫原性進行了評估,這是該公司第一階段研究中使用的第一批參與者,名為EBS-UFV-001。這一最新版本的Emergent通用流感候選疫苗包含多種成分,旨在誘導對甲型流感病毒的廣泛和反季節免疫。

"Emergent remains focused on investing in our diverse portfolio of R&D programs targeting infectious disease and other public health threats," said Kelly Warfield, Ph.D., senior vice president, research and development at Emergent BioSolutions. "Initiating this phase 1 study demonstrates our commitment to advancing our pipeline and our research and development team's scientific prowess to adopt an innovative technology and investigate a potential vaccine candidate for a disease that affects millions every year."

Emergent BioSolutions負責研究和開發的高級副總裁凱利·沃菲爾德博士説:“Emergent仍然專注於投資於我們針對傳染病和其他公共健康威脅的各種研發項目組合。啟動這項第一階段研究表明,我們致力於推進我們的管道,我們的研究和開發團隊具有采用創新技術並研究一種每年影響數百萬人的疾病的潛在候選疫苗的科學能力。“

The goal of this single-center, randomized, double blind, placebo-controlled dose-escalation study is to evaluate the safety, tolerability, and immunogenicity of the vaccine candidate at two dose levels and two schedules in 60 healthy adult individuals aged 18 to 45. This phase 1 study, being conducted in Australia, is fully funded by Emergent.

這項單中心、隨機、雙盲、安慰劑對照劑量遞增研究的目標是在60名18至45歲的健康成年人中評估兩種劑量水平和兩種方案的候選疫苗的安全性、耐受性和免疫原性。這項在澳大利亞進行的第一階段研究由Emergent全額資助。

Emergent's universal influenza vaccine candidate is based on a nanoparticle vaccine that self-assembles during production and that displays a cross-reactive hemagglutinin (HA) antigen for influenza virus A groups 1 and 2. The self-assembling HA stabilized stem nanoparticle technology was developed by and licensed from the National Institute of Allergy and Infectious Diseases Vaccine Research Center. Using this technology, a universal influenza vaccine could be designed to confer protection against divergent, constantly evolving strains and subtypes of influenza virus.i,ii,iii

Emergent的通用流感候選疫苗是基於一種納米顆粒疫苗,這種疫苗在生產過程中自組裝,顯示出對甲型流感病毒1組和2組具有交叉反應的血凝素(HA)抗原。自組裝HA穩定莖納米顆粒技術由美國國家過敏和傳染病疫苗研究中心開發並獲得許可。利用這項技術,可以設計一種通用的流感疫苗,以保護人們免受不同的、不斷進化的流感病毒株和亞型的影響。i,II,三、

For more information on the study, visit clinicaltrials.gov.

有關這項研究的更多信息,請訪問Clinicaltrials.gov。

About Seasonal Influenza
Seasonal influenza is an acute respiratory infection caused by influenza viruses which circulate in all parts of the world. There are four types of seasonal influenza viruses – types A, B, C, and D. Influenza A and B viruses circulate and cause seasonal epidemics of disease.

關於季節性流感
季節性流感是一種由在世界各地流行的流感病毒引起的急性呼吸道感染。季節性流感病毒有四種--A、B、C和D型。甲型和B型流感病毒傳播並引起疾病的季節性流行。

Seasonal influenza can be characterized by the sudden onset of fever, cough, headache, muscle and joint pain, severe malaise, sore throat and a runny nose. Most people recover from fever and other symptoms within a week without requiring medical attention. However, influenza can cause severe illness or death especially in people at high risk (e.g., pregnant women, children, the elderly, those with multiple medical comorbidities, and those immunocompromised).

季節性流感的特徵可能是突然發燒、咳嗽、頭痛、肌肉和關節疼痛、嚴重不適、喉嚨痛和流鼻涕。大多數人在一週內就會從發燒和其他症狀中恢復過來,不需要醫療護理。然而,流感可能導致嚴重疾病或死亡,特別是在高危人羣(例如:孕婦、兒童、老人、患有多種醫學合併症的人和免疫功能受損的人)。

According to the WHO, worldwide, these annual epidemics are estimated to result in 3 to 5 million cases of severe illness, and about 290,000 to 650,000 respiratory deaths.iv

根據世界衞生組織的數據,在全球範圍內,這些每年的流行病估計導致300萬至500萬例嚴重疾病,約29萬至65萬人死於呼吸道疾病。四.

About Emergent's Universal Influenza Vaccine
The goal of the final Emergent universal influenza vaccine candidate is to provide broad protection against multiple, divergent, and constantly evolving influenza virus A and B strains, including both seasonal and pandemic threats. The structure-based design of these vaccine components drives immune responses towards broadly cross-reactive and highly conserved antibody-recognized epitopes on the HA protein. The current EBS-UFV-001 phase 1 study is designed to demonstrate safety, tolerability, and immunogenicity of the influenza virus A components of the vaccine candidate with future studies planned to investigate additional components for full coverage against all influenza virus A and B strains.

關於Emergent公司的通用流感疫苗
最終的緊急通用流感候選疫苗的目標是提供廣泛的保護,以抵禦多種不同的、不斷進化的流感病毒A和B毒株,包括季節性和大流行威脅。這些疫苗成分的基於結構的設計驅使免疫反應朝向廣泛交叉反應和高度保守的HA蛋白上的抗體識別表位。目前的EBS-UFV-001第1階段研究旨在證明候選疫苗的A型流感病毒成分的安全性、耐受性和免疫原性,未來的研究計劃調查更多的成分,以全面覆蓋所有A型和B型流感病毒株。

About Emergent BioSolutions
Emergent BioSolutions is a global life sciences company whose mission is to protect and enhance life. Through our specialty products and contract development and manufacturing services, we are dedicated to providing solutions that address public health threats. Through social responsibility, we aim to build healthier and safer communities. We aspire to deliver peace of mind to our patients and customers so they can focus on what's most important in their lives. In working together, we envision protecting or enhancing 1 billion lives by 2030. For more information, visit our website and follow us on LinkedIn, Twitter, and Instagram.

關於緊急生物解決方案
Emerent BioSolutions是一家全球性生命科學公司,其使命是保護和提升生命。通過我們的專業產品以及合同開發和製造服務,我們致力於提供解決公共健康威脅的解決方案。通過社會責任,我們的目標是建設更健康、更安全的社區。我們渴望讓我們的患者和客户安心,這樣他們就可以專注於生活中最重要的事情。通過共同努力,我們設想到2030年保護或提高10億人的生命。有關更多信息,請訪問我們的網站,並在LinkedIn、Twitter和Instagram上關注我們。

Safe Harbor Statement
This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Any statements, other than statements of historical fact, including statements regarding the safety, tolerability and immunogenicity of the product candidate, executing on our development program, the success of our clinical trial, the inducement of broad and supra-seasonal immunity against influenza A, advancing our pipeline and potential solutions to combat influenza A and B, are forward-looking statements. These forward-looking statements are based on our current intentions, beliefs and expectations regarding future events. We cannot guarantee that any forward-looking statement will be accurate. The reader should realize that if underlying assumptions prove inaccurate or unknown risks or uncertainties materialize, actual results could differ materially from our expectations. Readers are, therefore, cautioned not to place undue reliance on any forward-looking statement. Any forward-looking statement speaks only as of the date of this press release, and, except as required by law, we do not undertake to update any forward-looking statement to reflect new information, events or circumstances.

安全港聲明
本新聞稿包括1995年“私人證券訴訟改革法”所指的前瞻性陳述。除有關歷史事實的陳述外,其他任何陳述,包括有關候選產品的安全性、耐受性和免疫原性、對我們的開發計劃的執行情況、我們臨牀試驗的成功、誘導對甲型流感的廣泛和反季節免疫、推進我們的管道以及抗擊甲型和乙型流感的潛在解決方案的聲明,都是前瞻性聲明。這些前瞻性陳述是基於我們目前對未來事件的意圖、信念和預期。我們不能保證任何前瞻性陳述都是準確的。讀者應該意識到,如果潛在的假設被證明是不準確的,或者未知的風險或不確定性成為現實,實際結果可能與我們的預期大不相同。因此,提醒讀者不要過度依賴任何前瞻性陳述。任何前瞻性陳述僅在本新聞稿發佈之日發表,除非法律另有要求,否則我們不承諾更新任何前瞻性陳述以反映新的信息、事件或情況。

There are a number of important factors that could cause the company's actual results to differ materially from those indicated by such forward-looking statements, including the success of this and other related clinical trials and the overall development program; the timing of and our ability to obtain and maintain regulatory approvals for the product candidate; and our commercialization, marketing and manufacturing capabilities. The foregoing sets forth many, but not all, of the factors that could cause actual results to differ from our expectations in any forward-looking statement. Readers should consider this cautionary statement, as well as the risk factors identified in our periodic reports filed with the SEC, when evaluating our forward-looking statements.

有許多重要因素可能會導致公司的實際結果與這些前瞻性陳述中顯示的結果大不相同,包括這次和其他相關臨牀試驗和整體開發計劃的成功;獲得和維持候選產品的監管批准的時機和能力;以及我們的商業化、營銷和製造能力。以上陳述了許多(但不是全部)可能導致實際結果與我們在任何前瞻性陳述中的預期不同的因素。讀者在評估我們的前瞻性聲明時,應考慮到這一警示性聲明,以及我們提交給美國證券交易委員會的定期報告中確定的風險因素。

i Kanekiyo, M. et al. Self-assembling influenza nanoparticle vaccines elicit broadly neutralizing H1N1 antibodies. Nature 499, 102-106 (2013).

iKanekiyo,M.等人。自組裝流感納米顆粒疫苗可誘導廣泛中和H1N1抗體。《自然》499,102-106(2013)。

ii Yassine, H. M. et al. Hemagglutinin-stem nanoparticles generate heterosubtypic influenza protection. Nat Med 21, 1065-1070 (2015).

IIYassine,H.M.等人。血凝素-莖納米粒可產生異型流感保護作用。NAT Med 21,1065-1070(2015)。

iii

三、

iv (seasonal)

四.(季節性)

Investor Contact:
Robert G. Burrows
Vice President, Investor Relations
240-631-3280
BurrowsR@ebsi.com

投資者聯繫方式:
羅伯特·G·布倫斯
投資者關係部副總裁
240-631-3280
郵箱:burrowsR@ebsi.com

Media Contact:
Matt Hartwig
Senior Director, Media Relations
mediarelations@ebsi.com

媒體聯繫人:
馬特·哈特威格
媒體關係部高級總監
郵箱:mediaRelations@ebsi.com


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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