Moderna Achieves Positive Interim Results from Phase 3 Trial of Next-Generation COVID-19 Vaccine

Moderna Achieves Positive Interim Results from Phase 3 Trial of Next-Generation COVID-19 Vaccine

  • mRNA-1283 caused a more robust immune reaction compared to Spikevax ® COVID-19 vaccine, mRNA-1273.222
  • Next-generation mRNA vaccine style uses the capacity of longer life span and storage benefits, and leads the way for mix vaccine versus influenza and COVID-19, mRNA-1083

Cambridge, MA, Mar 26, 2024 – (ACN Newswire) –Moderna, Inc. (NASDAQ: MRNA) today revealed that mRNA-1283, the Company’s next-generation COVID-19 vaccine, has actually effectively satisfied the main endpoints of its Phase 3 medical trial, showing a greater immune action versus SARS-CoV-2 when compared to mRNA-1273.222, Moderna’s certified COVID-19 vaccine.

“We are thrilled to reveal our 4th contagious illness vaccine program with favorable Phase 3 information, even more confirming our robust mRNA platform,” stated Stéphane Bancel, Chief Executive Officer of Moderna. “mRNA-1283 is a crucial part of our mix vaccine versus influenza and COVID-19, mRNA-1083, and this turning point offers us self-confidence in our capability to bring this much required vaccine to market.”

In the NextCOVE (NCT05815498) Phase 3 essential trial, mRNA-1283 was revealed to generate a greater immune action versus both the Omicron Bachelor’s Degree.4/ BACHELOR’S DEGREE.5 and initial infection pressures of SARS-CoV-2, compared to mRNA-1273.222. Notably, this advantage was most acutely seen in individuals over the age of 65 years, the population that stays at greatest threat for serious results from COVID-19. The most typical obtained regional unfavorable occasion was injection website discomfort. The most typical got systemic unfavorable occasions consisted of headache, tiredness, myalgia and chills.

The NEXTCovemedical trialis a randomized, observer-blind, active-controlled research study of roughly 11,400 people aged 12 years and older in the United States, United Kingdom and Canada. mRNA-1283 was discovered to have a comparable security profile to Moderna’s authorized COVID-19 vaccines.

The storage, life span and pre-filled syringe discussion of mRNA-1283 might ease doctor concern and possibly increase gain access to into brand-new settings to serve public health. An in-depth analysis of the Phase 3 scientific trial information for mRNA-1283 will be shared at the Company’s Vaccines Day occasion on March 27 and provided at upcoming clinical conferences.

About Moderna

Moderna is a leader in the production of the field of mRNA medication. Through the improvement of mRNA innovation, Moderna is reimagining how medications are made and changing how we deal with and avoid illness for everybody. By operating at the crossway of science, innovation and health for more than a years, the business has actually established medications at extraordinary speed and performance, consisting of among the earliest and most efficient COVID-19 vaccines.

Moderna’s mRNA platform has actually allowed the advancement of therapies and vaccines for contagious illness, immuno-oncology, uncommon illness and autoimmune illness. With a special culture and an international group driven by the Moderna worths and frame of minds to properly alter the future of human health, Moderna aims to provide the best possible effect to individuals through mRNA medications. To learn more about Moderna, please go tomodernatx.comand get in touch with us on X (previously Twitter), Facebook, Instagram, YouTube and LinkedIn.

Spikevax ® is a signed up hallmark of Moderna.

Positive Statements

This news release consists of positive declarations within the significance of the Private Securities Litigation Reform Act of 1995, as modified, consisting of declarations concerning: the prospective longer fridge life span and storage benefits of mRNA-1283 compared to Spikevax; and the capability of mRNA-1283 to keep efficiency compared to Spikevax. The positive declarations in this news release are neither pledges nor warranties, and you need to not position excessive dependence on these positive declarations since they include recognized and unidentified dangers, unpredictabilities, and other aspects, a lot of which are beyond Moderna’s control and which might trigger real outcomes to vary materially from those revealed or suggested by these positive declarations. These threats, unpredictabilities, and other elements consist of, to name a few, those threats and unpredictabilities explained under the heading “Risk Factors” in Moderna’s Annual Report on Form 10-K for the ended December 31, 2023, submitted with the U.S. Securities and Exchange Commission (SEC), and in subsequent filings made by Moderna with the SEC, which are readily available on the SEC’s site atwww.sec.govOther than as needed by law, Moderna disclaims any objective or duty for upgrading or modifying any positive declarations consisted of in this news release in case of brand-new details, future advancements or otherwise. These positive declarations are based upon Moderna’s existing expectations and speak just since the date of this news release.

Moderna Contacts

Media:
Elise Meyer
Sr. Director, Corporate Communications
+1 617-852-7041
Elise.Meyer@modernatx.com

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

SOURCE: Moderna, Inc.


Subject: Press release summary


Source: Moderna, Inc

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