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CureVac Announces Appointment of Dr. Malte Greune as Chief Operating Officer and Transition of Dr. Florian von der Mülbe to Lead Accelerated Development of The RNA Printer(R)

30 Jun 2021 12:00

CureVac / Key word(s): Personnel CureVac Announces Appointment of Dr. Malte Greune as Chief Operating Officer and Transition of Dr. Florian von der Mülbe to Lead Accelerated Development of The RNA Printer(R) 30.06.2021 / 13:00 The issuer is solely responsible for the content of this announcement.


CureVac Announces Appointment of Dr. Malte Greune as Chief Operating Officer and Transition of Dr. Florian von der Mülbe to Lead Accelerated Development of The RNA Printer(R)TÜBINGEN, Germany / BOSTON, USA - June 30, 2021 - CureVac N.V. (Nasdaq: CVAC), a global clinical-stage biopharmaceutical company developing a new class of transformative medicines based on messenger ribonucleic acid ("mRNA"), today announced the appointment of Dr. Malte Greune as Chief Operating Officer (COO) effective July 1, 2021. In this position, he will strengthen the company's Management Board and will head, among others, CureVac's clinical and commercial manufacturing activities. Dr. Greune joins CureVac with extensive experience in the global pharmaceutical industry, including manufacturing of vaccines and fill & finish of biologics.

CureVac also announced that Dr. Florian von der Mülbe, co-founder and Chief Production Officer, will now focus his extensive production expertise exclusively on the expansion and accelerated development of The RNA Printer(R), CureVac's solution for mobile, autonomous and fully automated manufacturing of GMP-grade RNA vaccines and therapeutics. To drive this key strategic project forward, which requires building its own operational infrastructure, Dr. von der Mülbe will resign from the Management Board of CureVac N.V.. Dr. Greune will assume Dr. von der Mülbe's position on the Management Board.

"On behalf of the Supervisory Board I would like to welcome Dr. Greune to the Management Board. Dr. Greune is a recognized expert in the global pharmaceutical industry with many years of experience in various management positions. His appointment is a great asset for CureVac as the company continues to grow, further expanding its one-stop shop strategy for RNA-based vaccines and therapeutics with strong manufacturing capabilities," said Jean Stéphenne, Chairman of the Supervisory Board of CureVac. "I would like to thank Dr. von der Mülbe for his service on the CureVac Management Board. As a co-founder of CureVac, he has played a key role in building the company and establishing its strong manufacturing expertise that he will now transition to ensure The RNA Printer(R) becomes another key growth driver for the company."

Dr. Greune joins CureVac from Sanofi-Aventis Deutschland GmbH where he held various management positions for almost ten years. As General Manager and Vice President Cartridges, Devices & Insulin Technology Group he was responsible for several manufacturing sites in Frankfurt. Under his leadership, six isolator filling lines for insulins, oncology drugs and biologics were set up including one for a COVID-19 vaccine. Prior to his position as Head of Diabetes, Oncology and Devices at Sanofi, he worked as Senior Vice President of Animal Health Manufacturing for the Merck Manufacturing Division, USA, where he led an international network of 28 sites - including 18 integrated vaccine sites. Furthermore, he held various leadership roles at the pharmaceutical companies Schering-Plough and Intervet International B.V.. Dr. Greune started his career at Hoechst AG in Corporate Planning.Dr. Greune received his Ph.D. in Economics from the University of Cologne, Germany, graduated from the University of Trier, Germany, and completed a Master of Business Administration at Clark University in Worcester, USA.

"Dr. Greune has a broad range of expertise in the international pharmaceutical sector which will benefit CureVac's growth even further," said Dr. Franz-Werner Haas, Chief Executive Officer of CureVac. "We are confident that his outstanding experience will support us in accelerating our development from a science-driven to a commercial pharmaceutical company. I would like to thank Dr. Florian von der Mülbe for combining founder's mindset with a growing commercialized company which he will continue to provide by the accelerated development of The RNA Printer(R)."

"Strong manufacturing capabilities represent an important part of our corporate strategy and I am proud of what we have built-up together in this area over the last 21 years," said Dr. Florian von der Mülbe. "I am happy that Dr. Greune is taking over to further develop our manufacturing capabilities and I am looking forward to using all my strength and expertise to rapidly drive forward The RNA Printer(R) as an accelerator of the RNA-field."

"It is a great pleasure to join CureVac at such an exciting phase of corporate transformation that centers on a diversified RNA-based product pipeline across different indications," added Dr. Malte Greune. "This technology is just starting to change today's medicine. I am looking forward to taking on this important task with the goal of bringing multiple mRNA drugs to market which may improve human health worldwide."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, the Company 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.

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.comCureVac Media ContactAnna Kamilli, Manager CommunicationsCureVac, Tübingen, GermanyT: +49 7071 9883-1684anna.kamilli@curevac.comBettina Jödicke-Braas, Manager CommunicationsCureVac, Tübingen, GermanyT: 49 7071 9883-1087bettina.joedicke-braas@curevac.com

Forward-Looking Statements

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 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.


30.06.2021 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:1213787
 
End of NewsDGAP News Service

1213787 30.06.2021 

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
11th Apr 202212:01 pmEQSCureVac and GSK Enter into Pandemic Preparedness Contract with German Government
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1st Mar 202212:01 pmEQSCureVac Establishes Fully-Owned Company Dedicated to Advancing The RNA Printer(R)
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17th Jan 202212:01 pmEQSCureVac Chief Technology Officer to Pursue New Career outside Biotech Industry
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18th Nov 20219:11 pmEQSCureVac veröffentlicht Finanzergebnisse für das dritte Quartal sowie die ersten neun Monate 2021 und informiert über das laufende Geschäft
18th Nov 202110:43 amEQSCureVac Publishes in Nature Preclinical Data of Second-Generation COVID-19 Candidate, CV2CoV, Demonstrating Comparable Antibody Levels to Licensed mRNA Vaccine
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10th Nov 202112:01 pmEQSCureVac Presents Promising Data at SITC from Phase 1 Study of Oncology Candidate CV8102 Showing Systemic Immune Response
10th Nov 202112:01 pmEQSCureVac präsentiert Daten auf SITC Konferenz aus Phase-1-Studie von Onkologie-Kandidat CV8102, die systemische Immunantwort zeigen
12th Oct 202112:03 pmEQSCureVac to Shift Focus of COVID-19 Vaccine Development to Second-Generation mRNA Technology
12th Oct 202112:03 pmEQSCureVac verlagert Fokus der COVID-19-Impfstoffentwicklung auf mRNA-Technologie der zweiten Generation
14th Sep 202112:20 pmRNSCureVac verschlankt europäisches Netzwerk zur mRNA-Produktherstellung
14th Sep 202112:20 pmRNSCureVac Streamlines European Network for mRNA Product Manufacturing
31st Aug 202112:00 pmEQSCureVacs Phase 2b/3-Studiendaten für CVnCoV auf Pre-Print-Server The Lancet veröffentlicht
31st Aug 202112:00 pmEQSCureVac's CVnCoV Phase 2b/3 Study Data Published in Preprints with The Lancet
30th Aug 202112:00 pmEQSCureVac-Studie: Präklinische Daten zeigen deutliche Verminderung von Leberfibrose mit mRNA-Therapeutikum
30th Aug 202112:00 pmEQSCureVac Preclinical Data Demonstrates Significant Reduction of Liver Fibrosis with mRNA Therapeutic
16th Aug 202112:11 pmEQSCureVac veröffentlicht Finanzergebnisse des zweiten Quartals und ersten Halbjahres 2021 und informiert über seine Geschäftsentwicklung
16th Aug 202112:11 pmEQSCureVac Announces Financial Results for the Second Quarter and First Half of 2021 and Provides Business Update
16th Aug 202112:00 pmEQSCureVac : Second-Generation mRNA COVID-19 Vaccine Candidate, CV2CoV, Demonstrates Improved Immune Response and Protection in Preclinical Study
16th Aug 202112:00 pmEQSCureVac : mRNA-basierter COVID-19-Impfstoffkandidat der zweiten Generation, CV2CoV, zeigt verbesserte Immunantwort und Schutzwirkung in präklinischer Studie
30th Jun 20219:30 pmEQSCureVac Final Data from Phase 2b/3 Trial of First-Generation COVID-19 Vaccine Candidate, CVnCoV, Demonstrates Protection in Age Group of 18 to 60
30th Jun 20219:30 pmEQSCureVacs Daten der finalen Analyse der Phase 2b/3-Studie für CVnCoV, den Impfstoffkandidaten der ersten Generation, zeigen Schutzwirkung in Altersgruppe von 18 bis 60 Jahren
30th Jun 202112:00 pmEQSCureVac gibt Ernennung von Dr. Malte Greune zum Chief Operating Officer und den Funktionswechsel von Dr. Florian von der Mülbe zur beschleunigten Weiterentwicklung des The RNA Printer(R) bekannt
30th Jun 202112:00 pmEQSCureVac Announces Appointment of Dr. Malte Greune as Chief Operating Officer and Transition of Dr. Florian von der Mülbe to Lead Accelerated Development of The RNA Printer(R)
24th Jun 20219:15 pmEQSCureVac Announces Voting Results of General Meeting
24th Jun 20219:15 pmEQSCureVac Announces Voting Results of General Meeting (English only)
23rd Jun 202112:30 pmEQSCureVac Provides Supervisory Board Update
23rd Jun 202112:30 pmEQSCureVac gibt personelle Änderungen im Aufsichtsrat bekannt
16th Jun 20219:42 pmEQSCureVac gibt Status-Update zur Phase 2b/3-Studie für Impfstoffkandidat der ersten Generation CVnCoV bekannt
16th Jun 20219:42 pmEQSCureVac Provides Update on Phase 2b/3 Trial of First-Generation COVID-19 Vaccine Candidate, CVnCoV
2nd Jun 202112:00 pmEQSCureVac Appoints Klaus Edvardsen as Chief Development Officer
2nd Jun 202112:00 pmEQSCureVac ernennt Klaus Edvardsen zum Chief Development Officer
28th May 20219:30 pmEQSCureVac's First-Generation COVID-19 Vaccine Candidate, CVnCoV, Continues Toward Phase 2b/3 Efficacy Readout in Variant-rich Environment Following DSMB Recommendation
28th May 20219:30 pmEQSCureVacs Impfstoffkandidat der ersten Generation, CVnCoV, setzt nach DSMB-Empfehlung in Phase 2b/3 Wirksamkeitsnachweis in variantengeprägtem Umfeld fort
26th May 202112:00 pmEQSCureVac Announces Financial Results for the First Quarter of 2021 and Business Updates
26th May 202112:00 pmEQSCureVac veröffentlicht Finanzergebnisse des ersten Quartals 2021 und informiert über seine Geschäftsentwicklung
12

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