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Second-Generation mRNA COVID-19 Vaccine Candidate, CV2CoV, Demonstrates Improved Immune Response and Protection in Preclinical Study Preclinical study provides evidence for strongly improved immune responses with second-

Key Takeaway: Second-Generation mRNA COVID-19 Vaccine Candidate, CV2CoV, Demonstrates Improved Immune Response and Protection in Preclinical Study T BINGEN, Germany/ BOSTON, USA/ London, United Kingdom - August 16, 2021 - CureVac N.V. (Nasdaq: CVAC), a global biopharmaceutical company devel

Full Press Release Details

Second-Generation mRNA COVID-19 Vaccine Candidate, CV2CoV, Demonstrates Improved Immune Response and Protection
in Preclinical Study
T BINGEN, Germany/ BOSTON, USA/ London, United Kingdom
- August 16, 2021 - CureVac N.V. (Nasdaq: CVAC), a global biopharmaceutical company developing a new class of
transformative medicines based on messenger ribonucleic acid ("mRNA"), and GSK today announced the publication of
preclinical data investigating immune responses as well as the protective efficacy of CureVac's first-generation vaccine
candidate, CVnCoV, and second-generation vaccine candidate, CV2CoV, against SARS-CoV-2 challenge in non-human primates. The study
assessed cynomolgus macaques vaccinated with 12 g of either the first or second-generation vaccine candidate. Better
activation of innate and adaptive immune responses was achieved with CV2CoV, resulting in faster response onset, higher titers of
antibodies and stronger memory B and T cell activation as compared to the first-generation candidate, CVnCoV. Higher antibody
neutralizing capacity was observed with CV2CoV across all selected variants, including the Beta, Delta and Lambda variants. During
challenge with the original SARS-CoV-2 virus, animals vaccinated with CV2CoV were found to be better protected based on highly
effective clearance of the virus in the lungs and nasal passages. The full manuscript of the preclinical data is available on the
preprint server bioRxiv.
"In this animal model, CV2CoV is shown to
induce broad antibody and cellular immune responses very similar to the breadth of the immune responses observed after infection with
SARS-CoV-2," said Dr. Igor Splawski, Chief Scientific Officer of CureVac. "The current study shows that the immune responses
and resulting protection produced by our second-generation candidate, based on our mRNA technology featuring targeted optimizations, are
substantially improved in non-human primates against both the original SARS-CoV-2 virus as well as the Beta and Delta Variants of Concern
and the Lambda Variant of Interest."
Dr. Rino Rappuoli, Chief Scientist and head of
GSK Vaccines R&D said: "The mRNA technology is a key strategic priority for us, and we are investing significantly in a number
of mRNA programs focused on the collaboration with CureVac. The strong immune response and protection in pre-clinical testing of this
second-generation mRNA backbone are very encouraging and represent an important milestone for its further development."
Within the study, CVnCoV and CV2CoV were
tested in cynomolgus macaques immunized with a 12 g dose of the respective candidate on day 0 and day 28. Induction of innate
immunity was investigated via specific cytokine markers. Adaptive immune responses were assessed based on receptor binding domain
specific antibodies and neutralizing antibodies as well as memory B and T cells. Impact of Variants of Concern and Variants of
Interest on neutralizing antibody titers was tested against the Alpha, Beta, Delta, Kappa and the Lambda variant. Clearance of the
virus in the lungs and nasal passages of the animals was tested following challenge infection with the original virus.
The CureVac-GSK COVID-19 collaboration announced
in February 2021 extends the existing strategic mRNA technology partnership both companies started in July 2020, which focuses on the
development of new products based on CureVac's second-generation mRNA-technology for different targets in the field of infectious
diseases. The optimized mRNA backbone that is being used in this collaboration also has the potential for a multivalent or combination
approach to address multiple emerging variants in one vaccine. Following the current preclinical development of CV2CoV, a Phase 1 clinical
trial is expected to start in Q4 2021.
CV2CoV is CureVac's first candidate based
on the advanced second-generation mRNA backbone currently developed in collaboration with GSK. The vaccine candidate, presently at a preclinical
development stage, is a non-chemically modified mRNA, encoding the prefusion stabilized full-length spike protein of the SARS-CoV-2 virus,
and formulated within Lipid Nanoparticles (LNPs). CV2CoV was engineered with specifically optimized non-coding regions to exhibit improved
mRNA translation for increased and extended protein expression compared the first-generation mRNA backbone. Preclinical studies in different
animal models demonstrate CV2CoV's ability to induce earlier and stronger immune responses. The first clinical trial of CV2CoV is
expected to start in Q4 2021.
CureVac is a global biopharmaceutical
company in the field of messenger RNA (mRNA) technology, with more than 20 years of expertise in developing and optimizing the versatile
biological molecule for medical purposes. The principle of CureVac's proprietary technology is the use of non-chemically modified mRNA
as a data carrier to instruct the human body to produce its own proteins capable of fighting a broad range of diseases. Based on its
proprietary technology, CureVac has built a deep clinical pipeline across the areas of prophylactic vaccines, cancer therapies, antibody
therapies, and the treatment of rare diseases. CureVac had its initial public offering on the New York Nasdaq in August 2020. It is headquartered
in T bingen, Germany, and employs more than 700 people at its sites in T bingen, Frankfurt, and Boston, USA. Further information
can be found at www.curevac.com.
GSK is a science-led global healthcare
company with a special purpose: to help people do more, feel better, live longer. For further information please visit www.gsk.com/about-us.
CureVac Investor Relations Contact
Dr. Sarah Fakih, Vice President Corporate Communications and Investor
CureVac, T bingen, Germany
T: +49 7071 9883-1298
M: +49 160 90 496949
CureVac Media Contact
Anna Kamilli, Manager Communications
CureVac, T bingen, Germany
T: +49 7071 9883-1684
Bettina J dicke-Braas, Manager Communications
CureVac, T bingen, Germany
T: 49 7071 9883-1087
GSK Enquiries
Media enquiries Simon Moore +44 (0) 20 8047 5502 (London)
Kristen Neese +1 804 217 8147 (Philadelphia)
Kathleen Quinn +1 202 603 5003 (Washington DC)
Analyst/Investor enquiries: James Dodwell +44 (0) 20 8047 2406 (London)
Sonya Ghobrial +44 (0) 7392 784784 (Consumer)
Mick Readey +44 (0) 7990 339653 (London)
Jeff McLaughlin +1 215 751 7002 (Philadelphia)
Frannie DeFranco +1 215 751 4855 (Philadelphia)
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 AG, CureVac Real Estate GmbH, CureVac Inc., CureVac Swiss AG and CureVac
Corporate Services GmbH (the "company") regarding future events or future results, in contrast with statements that
reflect historical facts. Examples include discussion of the potential efficacy of the company's vaccine and treatment
candidates and the company's strategies, financing plans, growth opportunities and market growth. In some cases, you can
identify such forward-looking statements by terminology such as "anticipate," "intend,"
"believe," "estimate," "plan," "seek," "project," or
"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, 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, reliance on key personnel, reliance on intellectual property protection,
ability to provide for patient safety, and fluctuations of operating results due to the effect of exchange rates or other factors.
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
For further information, please reference the company's reports
and documents filed with the U.S. Securities and Exchange Commission (SEC). You may get these documents by visiting EDGAR on the SEC website
Last updated: Aug 16, 2021