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R44AI140932

Project Grant

Overview

Grant Description
Development of a universal immunotherapeutic for influenza viruses.
Awardee
Funding Goals
NOT APPLICABLE
Place of Performance
Maryland United States
Geographic Scope
State-Wide
Analysis Notes
Amendment Since initial award the End Date has been extended from 02/29/20 to 09/30/24 and the total obligations have increased 529% from $290,038 to $1,825,591.
Abvacc was awarded Project Grant R44AI140932 worth $1,825,591 from the National Institute of Allergy and Infectious Diseases in March 2019 with work to be completed primarily in Maryland United States. The grant has a duration of 5 years 6 months and was awarded through assistance program 93.855 Allergy and Infectious Diseases Research. The Project Grant was awarded through grant opportunity PHS 2018-02 Omnibus Solicitation of the NIH, CDC, and FDA for Small Business Innovation Research Grant Applications (Parent SBIR [R43/R44] Clinical Trial Not Allowed).

SBIR Details

Research Type
SBIR Phase II
Title
Development of a Universal Immunotherapeutic for Influenza Viruses
Abstract
Project Summary Influenza virus (INFV) results in global seasonal and pandemic outbreaks estimated to cause severe illness in 3 to 5 million people annually resulting in significant morbidity and up to 650,000 deaths. The influenza burden also results in substantial economic loss. The goal of this program is to develop a therapeutic antibody offering effective treatment with broad heterosubtypic specificity for influenza viruses without inducing resistance. Our therapeutic antibody (3I14) has shown broad neutralizing activity against 14 strains of INFV A Groups 1 and 2 and both prophylactic and therapeutic protection in BALB/c mouse models of H1, H3, H5 and H7 serotypes. This Fast-track proposal is intended to establish a stable expressing cell line for manufacturing, identify an optimal product formulation, characterize the dose response and tolerability of the product in nonclinical studies, and complete the mouse efficacy data package. Completion of these milestones are critical for advancement to IND-enabling studies and clinical development. 3I14 binds the stem of both the uncleaved HA precursor and two mature forms of HA, either after trypsin activation alone or when followed by low-pH trigger. 3I14 prevents both the dissociation of HA1-HA2 and the pH-dependent HA rearrangement necessary for membrane fusion. Targeting the highly conserved HA stem epitope is also expected to drastically reduce the likelihood of viral resistance, a significant barrier to developing effective therapeutics for influenza. Integrated Biotherapeutics (IBT) has extensive experience in preclinical model and antibody product development for infectious diseases. Dr. Holtsberg and his team have extensive experience in providing services to pharma companies over the past 8 years in the development and use of in vitro assays and animal models for testing influenza therapies. This expertise is complimented by a strong strategic partnership with AbViro LLC with subject matter expertise specific to influenza and focus on integrated program management skillsets, extensive knowledge of preclinical product development and clinical science, regulatory expertise, and business and commercialization strategy for broad-spectrum antibodies capable of advancing 3I14 into clinical studies. IBT will also collaborate with MassBiologics, IIT Research Institute (IITRI) and La Jolla Institute for Allergy and Immunology (LJI). MassBiologics offers strong competency in stable cell line and manufacturing process development. IIT Research Institute (IITRI) provides relevant highly pathogenic influenza strains and animal models essential for rigorous evaluation of product efficacy. LJI provides core research functionality with next-generation sequencing capabilities. This development team has successfully advanced another broad-spectrum human monoclonal antibody targeting dengue virus to IND-enabling studies.Project Narrative Influenza virus (INFV) results in global seasonal and pandemic outbreaks estimated to cause severe illness in 3 to 5 million people annually and risk of mortality, particularly in young, elderly and immunocompromised populations. Annual vaccination efficacy, currently the most effective control measure, is limited by the requirement for annual reformulation and re-administration with variable efficacy. Potency of existing therapeutic drugs is limited by virus adaptation and emergence of new strains with limited susceptibility to existing drugs. The goal of this program is to develop our lead therapeutic antibody 3I14 offering broad heterosubtypic effective treatment for both Group 1 and 2 influenza A viruses regardless of group specificity, without inducing virus resistance. Completion of the proposed work will position 3I14 for advancement into IND-directed studies.
Topic Code
NIAID
Solicitation Number
PA18-574

Status
(Ongoing)

Last Modified 3/5/24

Period of Performance
3/14/19
Start Date
9/30/24
End Date
93.0% Complete

Funding Split
$1.8M
Federal Obligation
$0.0
Non-Federal Obligation
$1.8M
Total Obligated
100.0% Federal Funding
0.0% Non-Federal Funding

Activity Timeline

Interactive chart of timeline of amendments to R44AI140932

Transaction History

Modifications to R44AI140932

Additional Detail

Award ID FAIN
R44AI140932
SAI Number
R44AI140932-4172224254
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Small Business
Awarding Office
75NM00 NIH NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
Funding Office
75NM00 NIH NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
Awardee UEI
K5MSGRFGVVZ9
Awardee CAGE
9FDC1
Performance District
MD-90
Senators
Benjamin Cardin
Chris Van Hollen

Budget Funding

Federal Account Budget Subfunction Object Class Total Percentage
National Institute of Allergy and Infectious Diseases, National Institutes of Health, Health and Human Services (075-0885) Health research and training Grants, subsidies, and contributions (41.0) $1,311,436 100%
Modified: 3/5/24