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CureVac : Second-Generation mRNA COVID-19 Vaccine Candidate, CV2CoV, Demonstrates Improved Immune Response and Protection in Preclinical Study

16 Aug 2021 12:00

CureVac / Key word(s): Study results/Study CureVac : Second-Generation mRNA COVID-19 Vaccine Candidate, CV2CoV, Demonstrates Improved Immune Response and Protection in Preclinical Study 16.08.2021 / 13:00 The issuer is solely responsible for the content of this announcement.


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-generation mRNA backbone jointly developed by CureVac and GSK compared to CureVac's first-generation mRNA backbone Data demonstrate high protective efficacy of second-generation lead candidate, CV2CoV, in animal model during SARS-CoV-2 challenge study Neutralizing capacity of induced antibodies tested against a range of variants, including the Beta, Delta and Lambda variant

TÜBINGEN, 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 12µg 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 12µg 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.About CV2CoVCV2CoV 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.

About CureVacCureVac 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 Tübingen, Germany, and employs more than 700 people at its sites in Tübingen, Frankfurt, and Boston, USA. Further information can be found at www.curevac.com.About GSK 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 ContactDr. Sarah Fakih, Vice President Corporate Communications and Investor RelationsCureVac, Tübingen, GermanyT: +49 7071 9883-1298M: +49 160 90 496949sarah.fakih@curevac.com

CureVac Media ContactAnna Kamilli, Manager CommunicationsCureVac, Tübingen, GermanyT: +49 7071 9883-1684anna.kamilli@curevac.com

Bettina Jödicke-Braas, Manager CommunicationsCureVac, Tübingen, GermanyT: 49 7071 9883-1087bettina.joedicke-braas@curevac.com 

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 CureVacThis 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 law.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 at www.sec.gov.


16.08.2021 Dissemination of a Corporate News, transmitted by DGAP - a service of EQS Group AG.The issuer is solely responsible for the content of this announcement.The DGAP Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases. Archive at www.dgap.de


Language:English
Company:CureVac
Friedrich-Miescher-Str. 15
72076 Tübingen
Germany
EQS News ID:1226717
 
End of NewsDGAP News Service

1226717 16.08.2021 

corporate announcement transmitted by DGAP - a service of EQS Group AG. The issuer is solely responsible for the content of this announcement.

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Date   Source Headline
28th May 202412:01 pmEQSCureVac Announces Dosing of First Participant in a Phase 2 Study in Seasonal Influenza; Development in Collaboration with GSK
23rd May 202412:01 pmEQSCureVac Announces Financial Results for the First Quarter of 2024 and Provides Business Update
24th Apr 202412:08 pmEQSCureVac Announces Financial Results for the Fourth Quarter and Full-Year 2023 and Provides Business Update
24th Apr 202412:04 pmEQSCureVac Announces Start of Combined Phase 1/2 Study in Avian Influenza (H5N1); Development in Collaboration with GSK
24th Apr 202412:01 pmEQSCureVac Appoints Thaminda Ramanayake as New Chief Business Officer
18th Apr 202412:01 pmEQSCureVac to Report Fourth Quarter and Full-Year 2023 Financial Results and Business Update on April 24, 2024
16th Apr 202412:02 pmEQSCureVac and MD Anderson Enter Strategic Collaboration to Develop Novel Cancer Vaccines
4th Apr 202412:02 pmEQSCureVac Announces Promising Phase 2 Interim Data from Seasonal Influenza Vaccine Development Program in Collaboration with GSK
5th Jan 202412:02 pmEQSCureVac Announces Positive Phase 2 Interim Data from COVID-19 Vaccine Development Program in Collaboration with GSK Providing Strong Validation of Proprietary Technology Platform
19th Dec 20232:24 pmEQSCureVac Announces Decision of German Federal Patent Court in Broad Patent Litigation with BioNTech SE
14th Nov 202312:02 pmEQSCureVac Announces Financial Results for the Third Quarter and First Nine Months of 2023 and Provides Business Update
1st Nov 202312:02 pmEQSCureVac Announces Solid Progress in Phase 2 COVID-19 and Seasonal Flu Clinical Development Programs in Collaboration with GSK
28th Sep 202312:02 pmEQSCureVac Reports Progress in Intellectual Property Infringement Case Against BioNTech in Germany
12th Sep 202312:01 pmEQSCureVac Advances Seasonal Flu Study to Phase 2 in Collaboration with GSK Following Selection of Promising mRNA Vaccine Candidate with Broad Coverage
17th Aug 202312:01 pmEQSCureVac Announces Financial Results for the Second Quarter and First Half of 2023 and Provides Business Update
1st Aug 202312:01 pmEQSCureVac Announces Dosing of First Participant in Phase 2 Study of Modified COVID-19 mRNA Vaccine Candidates Developed in Collaboration with GSK
14th Jul 202312:01 pmEQSCureVac Announces Update to the Management Team
13th Jul 202312:01 pmEQSCureVac Strengthens Ongoing Patent Litigations Bringing Additional Cases Under New Intellectual Property Rights
20th Jun 202312:06 pmEQSCureVac Doses First Patient in Phase 1 Study of Cancer Vaccine Candidate for Surgically Resected Glioblastoma
20th Jun 202312:01 pmEQSCureVac Appoints International Financial Expert Michael Brosnan to Supervisory Board
19th Jun 20234:31 pmEQSCureVac Announces Voting Results of General Meeting
30th May 202312:01 pmEQSCureVac Announces Financial Results for the First Quarter of 2023 and Provides Business Update
19th May 202312:01 pmEQSCureVac Announces Developments in Patent Litigation with Pfizer/BioNTech
8th May 202312:01 pmEQSCureVac Announces Dosing of First Participant in Combined Phase 1/2 Study of Multivalent, Modified Influenza Vaccine Candidates Developed in Collaboration with GSK
25th Apr 202312:01 pmEQSCureVac Announces Financial Results for the Fourth Quarter and Full-Year 2022 and Provides Business Update
18th Apr 202312:01 pmEQSCureVac to Report Fourth Quarter and Full-Year 2022 Financial Results and Business Updates on April 25, 2023
28th Mar 20239:06 pmEQSCureVac Announces Voting Results of Extraordinary General Meeting
10th Feb 20239:05 pmEQSCureVac Announces Closing of $250 million Follow-on Public Offering of Common Shares
8th Feb 20231:04 amEQSCureVac Announces Pricing of Upsized Public Offering of Common Shares
6th Feb 20239:06 pmEQSCureVac Announces Proposed Public Offering of Common Shares
1st Feb 202312:00 pmEQSCureVac Welcomes Myriam Mendila as New Chief Development Officer
31st Jan 20231:13 pmEQSCureVac Named as One of the World’s Most Dynamic Innovators by LexisNexis®
30th Jan 202312:02 pmEQSCureVac Announces Positive Data in Older Adults from COVID-19 and Flu mRNA Vaccine Development Programs
9th Jan 202312:00 pmEQSCureVac Appoints Alexander Zehnder as CEO From April 1, 2023
6th Jan 202312:01 pmEQSCureVac Announces Positive Data on Joint COVID-19 and Flu mRNA Vaccine Development Programs
14th Dec 20229:05 pmEQSCureVac Members of Management Sell Shares to Cover Tax Obligations from Long Term Incentive Program
16th Nov 202212:00 pmEQSCureVac Announces Financial Results for the Third Quarter and First Nine Months of 2022 and Provides Business Update
11th Nov 202212:00 pmEQSCureVac Presents Preliminary Data from Phase 1 Study Expansion of Oncology Candidate CV8102
10th Nov 202212:00 pmEQSCureVac to Report Third Quarter and First Nine Months 2022 Financial Results and Business Updates on November 16, 2022
18th Aug 202212:06 pmEQSCureVac Announces Financial Results for the Second Quarter and First Half of 2022 and Provides Business Update
18th Aug 202212:01 pmEQSCureVac Starts Phase 1 Clinical Study of Modified, Omicron-Targeting COVID-19 Vaccine Candidate
5th Jul 202212:01 pmEQSCureVac Files Patent Infringement Lawsuit in Germany Against BioNTech
22nd Jun 20229:05 pmEQSCureVac Announces Voting Results of General Meeting
8th Jun 20229:10 pmEQSCureVac Accelerates Oncology Strategy with Acquisition of Frame Cancer Therapeutics, Adding Novel Antigen Discovery Platform
8th Jun 20229:05 pmEQSCureVac Announces Changes of CDO - Myriam Mendila to succeed Klaus Edvardsen
25th May 202212:06 pmEQSCureVac Announces Financial Results for the First Quarter of 2022 and Provides Business Update
25th May 202212:01 pmEQSCureVac Partners with myNEO to Identify Novel Antigen Targets for mRNA-Based Cancer Vaccine Development
28th Apr 202212:01 pmEQSCureVac Announces Financial Results for the Fourth Quarter and Full-Year 2021 and Provides Business Update
22nd Apr 202212:01 pmEQSCureVac to Report Fourth Quarter and Full-Year 2021 Financial Results and Business Updates on April 28, 2022
21st Apr 202212:01 pmEQSCureVac and GSK's Bivalent Second-Generation mRNA Vaccine Candidate Shown to be Highly Effective Against SARS-CoV-2 Variants in Preclinical Study
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