Establishment of the New York University Vaccine and Treatment Evaluation Unit (NYU VTEU)
- Funded by National Institutes of Health (NIH)
- Total publications:0 publications
Grant number: 3UM1AI148574-01S1
Grant search
Key facts
Disease
COVID-19Start & end year
20202022Known Financial Commitments (USD)
$9,214,781Funder
National Institutes of Health (NIH)Principal Investigator
Mark Joseph MulliganResearch Location
United States of AmericaLead Research Institution
New York University School Of MedicineResearch Priority Alignment
N/A
Research Category
Therapeutics research, development and implementation
Research Subcategory
Phase 3 clinical trial
Special Interest Tags
N/A
Study Type
Clinical
Clinical Trial Details
Clinical Trial, Phase III
Broad Policy Alignment
Pending
Age Group
Adults (18 and older)
Vulnerable Population
Unspecified
Occupations of Interest
Unspecified
Abstract
PROJECT Abstract: This supplement proposal outlines the scientific agenda for the COVID-19 Prevention Network (CoVPN)research to be carried out at the NYU VTEU. We will participate in the implementation of a COVID-19 vaccineefficacy trial "A Phase III Randomized, Double-blind, Placebo-controlled Multicenter Study in Adults toDetermine the Safety, Efficacy, and Immunogenicity of AZD1222, A Non-replicating ChAdOx1 Vector Vaccine,for the Prevention of COVID-19." In addition to the above, and as a supplement request to further address themission of the CoVPN, we are requesting funds for other CoVPN studies "and other COVID-related research".We plan to conduct an additional study within the CoVPN - Monoclonal Antibody (mAb) Studies: A Phase 3,Randomized, Double-Blind, Placebo-Controlled Study Assessing the Efficacy and Safety of Anti-Spike SARS-CoV-2 Monoclonal Antibodies in Preventing SARS-Cov-2 Infection in Household Contacts of IndividualsInfected with SARS-CoV-2.With the global COVID-19 pandemic, we recognize a significant need for vaccines that modify COVID-19 inSARS-CoV-2 infected individuals. The vaccine trial we will conduct is a phase 3, placebo-controlled, double-blinded study will test the efficacy of AZD1222, a recombinant replication-defective chimpanzee adenovirusexpressing the SARS-CoV-2 spike (S) surface glycoprotein, to modify COVID-19 disease in adults 18 year ofage and older. Participants will be recruited from up to 100 clinical trial sites across the US, using dataanalytics to target high risk individuals with a diverse racial and ethnic profile.The MAB study we will conduct is a pivotal phase 3 randomized, double-blind, placebo-controlled study inadults with household contact exposure to individuals with SARS-CoV-2 infection in geographic areas with anactive COVID-19 outbreak. An ideal agent for prophylaxis should be fast acting and highly effective and shouldprotect against multiple viral variants. A monoclonal antibody (mAb) combination therapy, with two differentmonoclonal antibodies that bind distinct regions of the portion of the SARS-CoV-2 spike (S) protein that bind toand facilitate entry into host cells, has been developed in order to achieve these goals. A mAb combinationagainst SARS-CoV-2 for post-exposure prophylaxis that can either prevent the development of disease orreduce viral acquisition or shedding could be key to reducing transmission of the virus and limiting symptomsand adverse outcomes following infection.We also request site preparedness funds, and fund for Dr Mulligan's role as national PI of an additional MABstudy (Lilly MAB in nursing home residents and staff, for COVID-19 prevention).