Consortium for Immunotherapeutics against Emerging Viral Threats
- Funded by National Institutes of Health (NIH)
- Total publications:0 publications
Grant number: unknown
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Key facts
Disease
COVID-19Start & end year
20202022Known Financial Commitments (USD)
$2,688,763Funder
National Institutes of Health (NIH)Principal Investigator
ERICA OLLMANN SAPHIREResearch Location
United States of AmericaLead Research Institution
LA JOLLA INSTITUTE FOR IMMUNOLOGYResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnostics
Research Subcategory
Pathogen genomics, mutations and adaptations
Special Interest Tags
N/A
Study Type
Non-Clinical
Clinical Trial Details
N/A
Broad Policy Alignment
Pending
Age Group
Not Applicable
Vulnerable Population
Not applicable
Occupations of Interest
Not applicable
Abstract
ABSTRACT We recently galvanized the Coronavirus Immunotherapeutic Consortium, CoVIC, an international effortto conduct side-by-side analyses of leading therapeutic antibody candidates against the SARS-CoV-2 Spikeprotein contributed by a range of large and small companies and academic labs on multiple continents. CoVICprovides an opportunity for side-by-side analysis of the leading therapeutic candidates under the same assayconditions, as well as real-time collaborative assembly of a broader, deeper dataset on the activities andpotencies of antibodies against SARS-CoV-2 than could be assembled by any single discovery effort alone. Thecurrently funded CoVIC studies focus largely on characteristics of the Fab region of the IgG therapeutic: bindingand mechanical neutralization, and analyze only spike from the original Wuhan reference strain of SARS-CoV-2. The proposed supplement will provide support for critical components that are currently missing from CoVICbut which are needed to accelerate clinical advancement of antibodies that will be safe, efficacious and offerdurable protection. We will determine Fc-mediated activities of the therapeutic antibodies, the likelihood or riskof enhancement from clinical candidates, and which epitopes and sites of and susceptibility to mutagenic escape.The resulting body of information will inform early and next-generation antibody therapies and will ensure thattherapeutics are known which are responsive to emerging viral variants.