About CureVac To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Information provided by (Responsible Party): Researchers are trying to assess the treatment potential and safety of anti-SARS-CoV-2 convalescent plasma in patients with acute respiratory symptoms with confirmed COVID-19. Da wir Ihr Recht auf Privatsphäre respektieren, können Sie sich dafür entscheiden, die Datenerfassung bei bestimmten Arten von Diensten nicht zuzulassen. Keywords provided by Michael J. Joyner, M.D., Mayo Clinic: Why Should I Register and Submit Results? The total number of days subjects were admitted to the hospital. The site you’re being redirected to is a branded pharmaceutical website. We strive to improve access and affordability, create healthier communities, and put a healthy mind, body and environment within reach of everyone, everywhere. CureVac N.V. (Nasdaq: CVAC), a clinical-stage biopharmaceutical company developing a new class of transformative medicines based on messenger ribonucleic acid (“mRNA”), announced today that the first participant has been dosed in a Phase 2a clinical trial of its COVID … During Relaxing Phase 1 there was no evidence of community spread within the territory. In clinical studies investigating vaccines, it is well known that vaccines often induce local and systemic side-effects that are mild, to moderate, and transient without consequences. Learn more at www.jnj.com. Vice President Communications, Dr. Sarah Fakih The full set of results will be published once the complete Phase 1/2a trial data are available. Here are the rules that apply in this phase. Initially scheduled to begin in September, the trial is now expected to commence in the second half of July. The forward-looking statements included in this press release are made only as of the date hereof. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. Phase 1 of Connecticut's Reopen Plan began on May 20, 2020. ... A Phase 2a, Randomized, Observer-Blind, Placebo Controlled, Dose-Confirmation Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of mRNA-1273 SARS-COV-2 Vaccine in Adults Aged 18 Years and Older: Use of this site constitutes your consent to application of such laws and regulations and to our Privacy Policy. The Company also plans on running a Phase 3 clinical trial of a two-dose regimen of JNJ-78436735 versus placebo later this year. Based on these findings, the single dose of the Janssen COVID-19 vaccine candidate of 5x1010 virus particles (vp) has been selected for further evaluation in the Phase 3 ENSEMBLE clinical trial. Available for Android and iOS devices. CureVac is a global biopharmaceutical company in the field of mRNA technology (messenger RNA). Risk Factors,” and in the company’s most recently filed Quarterly Report on Form 10-Q, and the company’s subsequent filings with the Securities and Exchange Commission. Phase 3 of Connecticut's Reopen Plan began on October 8, 2020. Female subjects with positive pregnancy test, breastfeeding, or planning to become pregnant/breastfeed during the study period, Receipt of pooled immunoglobulin in past 30 days, Contraindication to transfusion or history of prior reactions to transfusion blood products. The reader is cautioned not to rely on these forward-looking statements. For more information on Johnson & Johnson’s multi-pronged approach to combatting the pandemic, visit: www.jnj.com/coronavirus. Different dose strengths are being examined, starting with 6 µg. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances. About the Janssen Pharmaceutical CompaniesAt Janssen, we're creating a future where disease is a thing of the past. CureVac started its CVnCoV development program in January 2020. Strong contact tracing capabilities are in place, along with appropriate staffing levels to enforce social (physical) distancing requirements in all establishments and locations. The data demonstrate that a single dose of JNJ-78436735 induced a strong neutralizing antibody response in nearly all participants aged 18 years and older and was generally well-tolerated. The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. A further list and descriptions of these risks, uncertainties and other factors can be found in Johnson & Johnson's Annual Report on Form 10-K for the fiscal year ended December 29, 2019, including in the sections captioned “Cautionary Note Regarding Forward-Looking Statements” and “Item 1A. CureVac is headquartered in Tübingen, Germany with sites in Frankfurt and Boston, USA. Available for Android and iOS devices. For further information, please reference the company’s reports and documents filed with the U.S. Securities and Exchange Commission (SEC). You are now leaving jnj.com. After extensive pre-clinical development, the company started the clinical phase 1 study with its candidate at four study centers in Tübingen, Munich, Hanover and Ghent in June 2020. EEO Is the Law | EEO Is the Law GINA Supplement | Do Not Sell My Personal Information. We are blending our heart, science and ingenuity to profoundly change the trajectory of health for humanity. Two serious adverse events were reported, the first for hypotension which the investigator determined to not be vaccine related, and the second was a participant with a fever who was hospitalized due to suspicion of having COVID-19 but recovered within 12 hours. Pharma Advancement is a leading Pharma information centric website. Your use of the information on this site is subject to the terms of our Legal Notice. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. The reader is cautioned not to rely on these forward-looking statements. Drugs.com provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. Notice to Investors Concerning Forward-Looking Statements. Except as specified below, the provisions of all Mayor’s Orders concerning the COVID-19 public health emergency that are currently in effect shall continue to apply through December 31, 2020. Statements contained herein are made as of the date of this document unless stated otherwise, and neither the delivery of this document at any time, nor any sale of securities, shall under any circumstances create an implication that the information contained herein is correct as of any time after such date or that information will be updated or revised to reflect information that subsequently becomes available or changes occurring after the date hereof. However, these forward-looking statements are not a guarantee of the company’s performance, and you should not place undue reliance on such statements. NEW BRUNSWICK, N.J., June 10, 2020 – Johnson & Johnson (NYSE: JNJ) (the Company) today announced that through its Janssen Pharmaceutical Companies (Janssen) it has accelerated the initiation of the Phase 1/2a first-in-human clinical trial of its investigational SARS-CoV-2 vaccine, Ad26.COV2-S, recombinant.

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