Welcome to our dedicated page for Curevac B.V. news (Ticker: CVAC), a resource for investors and traders seeking the latest updates and insights on Curevac B.V. stock.
CureVac N.V. (NASDAQ: CVAC) is a multinational biopharmaceutical and biotech company focused on medicines based on messenger RNA (mRNA). Founded in 2000 and headquartered in Tübingen, Germany, CureVac describes itself as a pioneer in mRNA technology, with more than two decades of experience in developing, optimizing, and manufacturing mRNA for medical use. Its public communications highlight work in oncology precision immunotherapies, prophylactic vaccines, and mRNA-based treatments that aim to enable the body to produce therapeutic proteins.
The CVAC news feed features company announcements on clinical development milestones, regulatory decisions, intellectual property rulings, and financial results. Examples include updates on Phase 1 studies for off-the-shelf precision immunotherapies in glioblastoma and squamous non-small cell lung cancer, progress in a urinary tract infection vaccine program, and regulatory clearances such as U.S. FDA Investigational New Drug approvals and European Medicines Agency Clinical Trial Application decisions.
Investors and observers will also find news on patent litigation and IP protection, particularly proceedings at the European Patent Office and German courts involving patents that describe split poly-A tail technology, as well as agreements with BioNTech and Pfizer regarding mRNA-based COVID-19 vaccines. In addition, CureVac regularly reports quarterly and annual financial results, cash position, and the effects of restructuring and licensing agreements with partners like GSK and CRISPR Therapeutics.
Recent releases describe a definitive purchase agreement under which BioNTech intends to acquire all shares of CureVac via a public exchange offer, along with shareholder voting results and steps toward a post-offer reorganization. For anyone tracking CVAC, this news page provides a centralized view of CureVac’s scientific, clinical, legal, financial, and corporate developments over time.
CureVac N.V. (Nasdaq: CVAC) announced the enrollment of the first participant in its Phase 2b/3 study for its mRNA vaccine candidate, CVnCoV, targeting COVID-19. This pivotal trial, named HERALD, plans to enroll over 35,000 participants across Europe and Latin America, assessing vaccine safety and efficacy at a 12 µg dose. The study aims to prevent confirmed COVID-19 cases and includes a long-term monitoring phase for safety and efficacy. Previous trials showed promising immunogenicity and tolerability for CVnCoV.
CureVac (NASDAQ:CVAC) appointed Antony Blanc, PhD, as Chief Business Officer and Chief Commercial Officer, effective immediately. Blanc brings extensive experience in biotech and vaccines, previously serving roles at McKinsey & Company and GSK Vaccines. His expertise in RNA research is expected to enhance CureVac's business development and growth. The company is advancing its mRNA-based COVID-19 vaccine, CVnCoV, with promising Phase 1 interim data indicating strong antibody responses. CureVac is also expanding manufacturing capacities to prepare for commercial supply.
CureVac (NASDAQ: CVAC) reported promising interim Phase 1 data for its COVID-19 vaccine candidate, CVnCoV, demonstrating strong antibody responses and T-cell activation. The company secured an agreement with the European Commission to supply 225 million doses, with an option for 180 million more. CureVac reported a cash position of €892 million and revenues of €5.2 million for Q3 2020, marking a 371% increase year-over-year. The company plans to initiate a pivotal Phase 2b/3 trial shortly, aiming to expand its vaccine capabilities and address the ongoing pandemic.
CureVac N.V. (Nasdaq:CVAC) will report its financial results and business updates for Q3 and the first nine months of 2020 on November 30, 2020. A conference call and webcast will occur at 4:00 p.m. CET / 10:00 a.m. EST with details provided for participation. This follows the company's IPO in August 2020, marking its entry into the public market. CureVac focuses on mRNA technology, with a pipeline in vaccines, cancer therapies, and rare diseases. The company has over 500 employees and is headquartered in Tübingen, Germany.
CureVac N.V. (NASDAQ:CVAC) has announced plans to expand its manufacturing capabilities for the COVID-19 vaccine candidate, CVnCoV, aiming for up to 300 million doses in 2021 and 600 million doses in 2022. This initiative involves building a European vaccine manufacturing network with experienced partners to mitigate supply chain risks. The company is in the process of finalizing technology transfers and establishing partnerships with various CDMO firms across Europe, enhancing production resilience.
CureVac (Nasdaq:CVAC) announced that the European Commission will authorize an Advanced Purchase Agreement for its mRNA-based COVID-19 vaccine candidate, CVnCoV. The contract encompasses 225 million initial doses, with an option for an additional 180 million doses. An upfront payment will support advanced clinical development and ramp-up of manufacturing capabilities. CVnCoV is undergoing pivotal Phase 2b/3 clinical trials, following promising Phase 1 data indicating strong immune responses. CureVac aims to provide equitable access to its vaccine globally.
CureVac N.V. (NASDAQ: CVAC) has published detailed interim Phase 1 data for its COVID-19 vaccine candidate, CVnCoV, following positive topline results reported on November 2, 2020. The data highlights that CVnCoV was well tolerated across doses (2-12μg) and induced robust antibody responses, mimicking immune responses in recovered COVID-19 patients. The manuscript is available on medRxiv. A conference call is scheduled for today at 5 p.m. CET to discuss the data further, with plans for a pivotal Phase 2b/3 trial by year-end.
CureVac N.V. (NASDAQ:CVAC) reported positive interim data from its Phase 1 study of CVnCoV, a COVID-19 vaccine candidate. The vaccine demonstrated a balanced immune response, inducing strong binding and neutralizing antibodies, alongside initial T cell activation. Results showed that the immune response is comparable to that of recovered COVID-19 patients. With the 12µg dose showing the most promise, CureVac plans to advance to a pivotal Phase 2b/3 clinical trial by the end of 2020, having already administered doses to over 250 participants.
CureVac N.V. (NASDAQ: CVAC) reported positive preclinical results for its COVID-19 vaccine candidate, CVnCoV. The vaccine induced strong antibody and T cell responses in animal models, effectively protecting against SARS-CoV-2 with a favorable safety profile. Notably, hamsters showed significant reduction in viral load and complete lung protection after vaccination. CureVac continues its Phase 1 and 2a clinical trials, with interim data expected soon. The company aims to scale up production capabilities for potential commercial supply.
CureVac N.V. (NASDAQ:CVAC) has initiated its Phase 2a clinical trial for the COVID-19 vaccine candidate, CVnCoV, with the first participant dosed in Peru and Panama. Enrolling 690 participants, the trial targets both younger adults (18-60 years) and older adults (61+ years). The study aims to confirm safety and reactogenicity while assessing the immune response in a high COVID-19 incidence area. Results are expected by Q4 2020. This trial follows the positive preliminary data from an ongoing Phase 1 study in Europe, and a larger Phase 2b/3 trial is planned for later this year.
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