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Moderna and CEPI Expand Strategic Collaboration to Advance Potential Vaccine Against Bundibugyo Ebolavirus

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Moderna (NASDAQ:MRNA) and CEPI expanded their collaboration to advance a potential Bundibugyo ebolavirus (BDBV) vaccine. CEPI committed up to $50 million to fund preclinical work, Phase 1 clinical testing, and parallel manufacturing using Moderna's mRNA platform.

The goal is to accelerate readiness for rapid progression to Phase 2/3 trials if Phase 1 safety and immunogenicity data support further development.

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AI-generated analysis. Not financial advice.

Positive

  • CEPI commits up to $50 million for Moderna’s BDBV vaccine program
  • Funding supports preclinical studies and Phase 1 clinical evaluation
  • Parallel manufacturing funding may enable faster transition to Phase 2/3 trials
  • Collaboration deepens Moderna–CEPI partnership in epidemic preparedness
  • Leverages Moderna’s proven mRNA platform and filovirus research experience

Negative

  • BDBV vaccine candidate remains at preclinical and Phase 1 development stage
  • Future progression to Phase 2/3 depends on favorable Phase 1 safety and immunogenicity data

Key Figures

CEPI funding commitment: up to US $50 million Phase 1: Phase 1 Phase 2/3: Phase 2/3 +3 more
6 metrics
CEPI funding commitment up to US $50 million Supports preclinical development and Phase 1 clinical testing of BDBV vaccine
Phase 1 Phase 1 Initial clinical evaluation of investigational Bundibugyo ebolavirus vaccine
Phase 2/3 Phase 2/3 Potential large-scale trials if Phase 1 safety and immunogenicity support advancement
Suspected cases more than 900 suspected cases Current Bundibugyo ebolavirus outbreak size
Suspected deaths more than 220 suspected deaths Fatalities in current Bundibugyo ebolavirus outbreak
Outbreak ranking third largest Filovirus outbreak Historical ranking of the current outbreak by size

Market Reality Check

Price: $47.19 Vol: Volume 6,228,409 is below...
normal vol
$47.19 Last Close
Volume Volume 6,228,409 is below the 20-day average of 7,922,080 (relative volume 0.79x). normal
Technical Price 47.19 is trading above the 200-day MA of 37.48, indicating a pre-existing uptrend.

Peers on Argus

MRNA was down 0.8% while close peers showed mixed moves (e.g., ROIV -1.05%, HALO...
2 Up 1 Down

MRNA was down 0.8% while close peers showed mixed moves (e.g., ROIV -1.05%, HALO -2.49%, MDGL -3.36%, VRNA and BPMC slightly positive). Momentum scanner flags were split (RVMD up, JAZZ down, HALO up), supporting a stock-specific rather than sector-wide move.

Previous Partnership Reports

4 past events · Latest: Feb 10 (Positive)
Same Type Pattern 4 events
Date Event Sentiment Move Catalyst
Feb 10 Government vaccine pact Positive +0.1% Five-year Mexico agreement for access and tech transfer of mRNA vaccines.
Jan 29 Commercialization deal Positive -6.0% Recordati collaboration on mRNA-3927 with upfront and milestone economics.
Aug 28 Target discovery pact Neutral -0.8% Platform-based collaboration for novel cardiovascular and renal disease targets.
Jul 02 BARDA funding award Positive +1.0% BARDA project award to accelerate mRNA-based pandemic influenza vaccine work.
Pattern Detected

Partnership headlines have often produced muted or negative next-day moves despite generally constructive strategic content.

Recent Company History

Recent history for Moderna shows multiple strategic collaborations in vaccines and therapeutics. A BARDA project award in July 2024 and a Mexico pandemic-preparedness agreement in February 2026 supported its respiratory and COVID-19 franchises. The Recordati deal in January 2026 advanced an mRNA rare-disease program with defined economics, while another 2024 partnership focused on target discovery in cardiovascular and renal diseases. Today’s CEPI-funded Bundibugyo ebolavirus program fits this pattern of external, non-dilutive support for infectious-disease preparedness.

Historical Comparison

-1.4% avg move · Partnership headlines for MRNA have averaged a -1.42% next-day move, suggesting that similar collabo...
partnership
-1.4%
Average Historical Move partnership

Partnership headlines for MRNA have averaged a -1.42% next-day move, suggesting that similar collaboration news has historically led to modest or negative price reactions.

Partnership news shows a progression from government pandemic-preparedness deals and BARDA funding to commercial collaborations and target-discovery alliances, underscoring a strategy of using external partners and funding to advance vaccines and mRNA therapeutics.

Market Pulse Summary

This announcement highlights CEPI’s commitment of up to US $50 million to support preclinical and Ph...
Analysis

This announcement highlights CEPI’s commitment of up to US $50 million to support preclinical and Phase 1 development of Moderna’s Bundibugyo ebolavirus vaccine, along with parallel manufacturing to enable rapid progression to potential Phase 2/3 trials. It extends a pattern of partnerships funding pandemic preparedness. Investors may watch clinical safety and immunogenicity data, outbreak evolution, and how this program complements Moderna’s broader infectious-disease pipeline.

Key Terms

mrna, filoviruses, phase 1, phase 2/3, +1 more
5 terms
mrna medical
"The vaccine candidate is being developed using Moderna's mRNA platform"
mRNA, short for messenger ribonucleic acid, is a biological molecule that carries instructions from a cell’s genetic blueprint to make specific proteins — like a recipe or software code that tells a kitchen or computer what to produce. Investors care because mRNA is used as a flexible drug and vaccine platform that can be developed and scaled faster than many traditional medicines; its commercial prospects, manufacturing needs, regulatory approval path, and patent position can strongly affect a company’s value.
filoviruses medical
"builds on Moderna's existing research and development efforts in filoviruses"
Filoviruses are a family of viruses that can cause severe, rapidly progressing illness in humans and animals, often involving high fever and bleeding; they include well-known types that trigger intense public health responses. For investors, outbreaks or research breakthroughs can quickly affect sectors like biotechnology, diagnostics, travel and insurance because they drive urgent demand for treatments, accelerate regulatory action and reshape risk perceptions much like a sudden storm that forces companies and markets to change course.
phase 1 medical
"supports preclinical development and Phase 1 clinical evaluation"
Phase 1 is the first stage of testing a new drug or medical treatment in people, focused primarily on safety, how the body handles the product, and finding a tolerated dose. Think of it as a short, tightly controlled experiment with a small group to check for dangerous side effects before wider testing; for investors it is an early milestone that reduces some uncertainty but still carries high risk and potential for both big value changes and setbacks.
phase 2/3 medical
"advance into large-scale Phase 2/3 trials should the Phase 1 data support"
A phase 2/3 trial is a combined clinical study that first evaluates how well a treatment works and the best dose, then expands into a larger test to confirm those results and safety. For investors, it matters because moving into a phase 2/3 signals that an experimental therapy has shown initial promise and will be tested at scale, which can materially change the odds and timeline for regulatory approval and commercial potential.
public health emergency of international concern (pheic) regulatory
"declared a Public Health Emergency of International Concern (PHEIC)"
A public health emergency of international concern (PHEIC) is an official declaration by the World Health Organization that a disease outbreak poses a serious risk beyond one country and needs coordinated global action. For investors it signals potential widespread disruptions — like travel limits, supply-chain interruptions, surges in healthcare demand and policy responses — so it can affect market sentiment, sector performance and short- to medium-term company operations.

AI-generated analysis. Not financial advice.

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Coalition for Epidemic Preparedness Innovations funding builds on Moderna's prior filovirus research and supports preclinical development and Phase 1 clinical evaluation

CAMBRIDGE, MA / ACCESS Newswire / June 1, 2026 / Moderna, Inc. (NASDAQ:MRNA) today announced an expanded collaboration with the Coalition for Epidemic Preparedness Innovations (CEPI) to advance the development of a potential vaccine against Bundibugyo ebolavirus (BDBV), a cause of Ebola virus disease for which there are currently no licensed vaccines indicated.

Under the agreement, CEPI has committed up to US $50 million to support preclinical development and Phase 1 clinical testing of Moderna's investigational BDBV vaccine candidate. The funding will also support parallel manufacturing activities, enabling doses to be produced while clinical evaluation is underway and positioning the program to rapidly advance into large-scale Phase 2/3 trials should the Phase 1 safety and immunogenicity data support further development.

The vaccine candidate is being developed using Moderna's mRNA platform, the same technology that demonstrated rapid development, scalability, and global deployment capabilities during the COVID-19 pandemic. The program also builds on Moderna's existing research and development efforts in filoviruses, including Ebola-related viruses.

The collaboration further expands Moderna's longstanding strategic collaboration with CEPI, which is focused on accelerating the development of vaccines and other countermeasures against epidemic and pandemic threats.

"At Moderna, we believe our mRNA platform can play an important role in responding rapidly to emerging infectious disease threats," said Stéphane Bancel, Chief Executive Officer of Moderna. "We are proud to expand our strategic collaboration with CEPI to advance a potential vaccine candidate against Bundibugyo ebolavirus, leveraging our established technology and experience in filovirus vaccine development. We will move with urgency and scientific rigor to support the response and help bring a potential vaccine closer to the communities that need it most."

By combining CEPI's funding and expertise in epidemic preparedness with Moderna's mRNA platform and manufacturing capabilities, the collaboration aims to accelerate the development of a potential vaccine that could help strengthen global readiness against future Ebola outbreaks.

"With Bundibugyo virus spreading rapidly and no licensed vaccines, every day counts in the race against this deadly disease," said Dr. Richard Hatchett, CEO of CEPI. "CEPI's urgent funding and support aims to advance safe, effective vaccines to help control this epidemic."

The current outbreak - declared a Public Health Emergency of International Concern (PHEIC) and a Public Health Emergency of Continental Security (PHECS) by the World Health Organization and Africa CDC, respectively - has already caused more than 900 suspected cases and more than 220 suspected deaths, making it the third largest Filovirus outbreak in history.

About Moderna

Moderna is a pioneer and leader in the field of mRNA medicine. Through the advancement of its technology platform, Moderna is reimagining how medicines are made to transform how we treat and prevent diseases. Since its founding, Moderna's mRNA platform has enabled the development of vaccines and therapeutics across infectious diseases, cancer, rare diseases and more.

With a global team and a unique culture, driven by the company's values and mindsets, Moderna's mission is 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, Facebook, Instagram, YouTube and LinkedIn.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including statements regarding: Moderna's expanded collaboration with CEPI and CEPI's investment; the ability to rapidly advance into large-scale Phase 2/3 trials; the potential for a vaccine against BDBV. In some cases, forward-looking statements can be identified by terminology such as "will," "may," "should," "could," "expects," "intends," "plans," "aims," "anticipates," "believes," "estimates," "predicts," "potential," "continue," or the negative of these terms or other comparable terminology, although not all forward-looking statements contain these words. 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, 2025, filed with the U.S. Securities and Exchange Commission (SEC), and in subsequent filings made by Moderna with the SEC, 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.

Moderna Contacts

Media:

Chris Ridley
Vice President, Global Head of Communications
+1 617-800-3651
Chris.Ridley@modernatx.com

Investors:

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

SOURCE: Moderna, Inc.



View the original press release on ACCESS Newswire

FAQ

What did Moderna (MRNA) announce on June 1, 2026 about its Bundibugyo ebolavirus vaccine?

Moderna announced an expanded collaboration with CEPI to develop a potential Bundibugyo ebolavirus vaccine. According to Moderna, CEPI will provide up to $50 million for preclinical work, Phase 1 trials, and parallel manufacturing to accelerate development.

How much funding is CEPI providing to Moderna (MRNA) for the Bundibugyo ebolavirus vaccine program?

CEPI committed up to $50 million to Moderna’s investigational Bundibugyo ebolavirus vaccine. According to Moderna, this funding will support preclinical development, Phase 1 clinical evaluation, and manufacturing activities conducted in parallel with early trials to speed potential scale-up.

What development stage will Moderna’s Bundibugyo ebolavirus (MRNA) vaccine reach under the CEPI agreement?

The CEPI agreement funds preclinical development and a Phase 1 clinical trial of Moderna’s BDBV vaccine. According to Moderna, the data from Phase 1 safety and immunogenicity studies will determine whether the program advances into larger Phase 2/3 trials.

How does Moderna’s mRNA platform support the new Bundibugyo ebolavirus vaccine (MRNA)?

Moderna is using its mRNA platform for the investigational Bundibugyo ebolavirus vaccine. According to Moderna, this technology previously enabled rapid development, scalability, and global deployment during COVID-19, and now underpins the company’s broader filovirus and epidemic-preparedness research.

What is the strategic importance of Moderna and CEPI’s expanded collaboration for MRNA investors?

The expanded collaboration strengthens Moderna’s role in epidemic and pandemic preparedness. According to Moderna, CEPI funding and expertise combined with its mRNA and manufacturing capabilities aim to accelerate a BDBV vaccine, potentially enhancing the company’s infectious-disease vaccine portfolio over time.

Will Moderna’s Bundibugyo ebolavirus vaccine (MRNA) move quickly into Phase 2/3 trials?

Progression to Phase 2/3 is not guaranteed and depends on Phase 1 results. According to Moderna, parallel manufacturing could position the program to advance rapidly if Phase 1 safety and immunogenicity data are supportive of further clinical development.