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CureVac Receives Additional Positive Validity Decision from European Patent Office in Ongoing Litigation Against BioNTech SE European Patent Office largely dismisses opposition filed by BioNTech SE, Pfizer Inc., and othe

Key Takeaway: CureVac Receives Additional Positive Validity Decision from European Patent Office in Ongoing Litigation Against BioNTech SE T BINGEN, Germany/BOSTON, USA - May 15, 2025 - CureVac N.V. (Nasdaq: CVAC) ("CureVac"), a global biotech company developing a new class of transformati

Full Press Release Details

CureVac Receives Additional Positive Validity
Decision from European Patent Office
in Ongoing Litigation Against BioNTech SE
T BINGEN, Germany/BOSTON, USA -
May 15, 2025 - CureVac N.V. (Nasdaq: CVAC) ("CureVac"), a global biotech company developing a new class of transformative
medicines based on messenger ribonucleic acid ("mRNA"), today announced that the European Patent Office (EPO) has confirmed
the validity of CureVac's European patent EP 4 023 755 B1 subject to amendments to specify the scope of protection. This validity
decision marks the second time the EPO has ruled in favor of CureVac, having decided in March to uphold the validity of patent EP 3 708
668 B1 also in amended form.
Following today's hearing, the EPO opposition
division dismissed the oppositions and maintained the patent in amended form.
The ruling signals a positive development for
CureVac in the ongoing patent litigation with BioNTech in Germany. The dispute encompasses a total of six intellectual property rights.
With the validity of patent EP 4 023 755 B1 upheld in amended form, the Regional Court D sseldorf will decide whether the patent
in its amended form has been infringed. In the same hearing, taking place on July 1, 2025, the Court will hear the arguments on infringement
of EP 3 708 668 B1, with a decision to come at a later date. A positive infringement decision on either or both patents would trigger
proceedings to assess damages in the same court.
Like EP 3 708 668 B1, patent EP 4 023 755 B1 describes
split poly-A tail technology, which enhances medical efficacy by improving expression of the protein encoded on an mRNA construct, a foundational
invention of CureVac.
CureVac is represented in Germany by Oliver Jan
J ngst from Bird & Bird LLP and Andreas Graf von Stosch from Graf von Stosch Patentanwaltsgesellschaft and represented in the
U.S. by Mark H. Izraelewicz from Marshall, Gerstein & Borun LLP and John M. Erbach from Spotts Fain, PC.
CVAC) is a pioneering multinational biotech company founded in 2000 to advance the field of messenger RNA (mRNA) technology for application
in human medicine. In more than two decades of developing, optimizing, and manufacturing this versatile biological molecule for medical
purposes, CureVac has introduced and refined key underlying technologies that were essential to the production of mRNA vaccines against
COVID-19, and is currently laying the groundwork for application of mRNA in new therapeutic areas of major unmet need. CureVac is leveraging
mRNA technology, combined with advanced omics and computational tools, to design and develop off-the-shelf and personalized cancer vaccine
product candidates. It also develops programs in prophylactic vaccines and in treatments that enable the human body to produce its own
therapeutic proteins. Headquartered in T bingen, Germany, CureVac also operates sites in the Netherlands, Belgium, Switzerland,
and the U.S. Further information can be found at www.curevac.com.
Media and Investor Relations Contact
Corporate Communications and Investor Relations
Forward-Looking Statements CureVac
This press release contains statements that constitute "forward
looking statements" as that term is defined in the United States Private Securities Litigation Reform Act of 1995, including statements
that express the opinions, expectations, beliefs, plans, objectives, assumptions or projections of CureVac N.V. and/or its wholly owned
subsidiaries CureVac SE, CureVac Manufacturing GmbH, CureVac Inc., CureVac Swiss AG, CureVac Corporate Services GmbH, CureVac Belgium
SA and CureVac Netherlands B.V. (the "company") regarding future events or future results, in contrast with statements that
reflect historical facts. Examples include discussion of the strength of the company's intellectual property portfolio and plans
for resolving certain intellectual property matters, potential efficacy of the company's vaccine and treatment candidates and the
company's strategies and court judgements. In some cases, you can identify such forward-looking statements by terminology such as
"anticipate," "intend," "believe," "estimate," "plan," "seek,"
"project," "expect," "may," "will," "would," "could," "potential,"
"intend," or "should," the negative of these terms or similar expressions. Forward-looking statements are based
on management's current beliefs and assumptions and on information currently available to the company. However, these forward-looking
statements are not a guarantee of the company's performance, and you should not place undue reliance on such statements. Forward-looking
statements are subject to many risks, uncertainties and other variable circumstances, including negative worldwide economic conditions
and ongoing instability and volatility in the worldwide financial markets, ability to obtain funding, ability to conduct current and future
preclinical studies and clinical trials, the timing, expense and uncertainty of regulatory approval, reliance on third parties and collaboration
partners, ability to commercialize products, ability to manufacture any products, ability to implement our pipeline strategy, possible
changes in current and proposed legislation, regulations and governmental policies, pressures from increasing competition and consolidation
in the company's industry, the effects of the COVID-19 pandemic on the company's business and results of operations, ability
to manage growth, ability to implement, maintain and improve effective internal controls, reliance on key personnel, reliance on intellectual
property protection and the company's and the company's collaborators' ability to obtain, maintain, defend and enforce
such intellectual property, scope of intellectual property protection, ability to provide for patient safety, fluctuations of operating
results due to the effect of exchange rates, delays in litigation proceedings, different judicial outcomes factors and other important
factors discussed under the caption "Risk Factors" in the company's annual report on Form 20-F filed with the U.S. Securities
and Exchange Commission (the "SEC") on April 11, 2025, as such factors may be updated form time to time in its other filings
with the SEC. Such risks and uncertainties may cause the statements to be inaccurate and readers are cautioned not to place undue reliance
on such statements. Many of these risks are outside of the company's control and could cause its actual results to differ materially
from those it thought would occur. The forward-looking statements included in this press release are made only as of the date hereof.
The company does not undertake, and specifically declines, any obligation to update any such statements or to publicly announce the results
of any revisions to any such statements to reflect future events or developments, except as required by law.
For further information, please reference the
company's reports and documents filed with the U.S. Securities and Exchange Commission (the "SEC"). You may get these
documents by visiting EDGAR on the SEC website at www.sec.gov.
Last updated: May 15, 2025