SBIR-STTR Award

Synthetic Universal Flu Vaccine
Award last edited on: 11/4/2019

Sponsored Program
SBIR
Awarding Agency
NIH : NCIRD
Total Award Amount
$224,966
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Christopher H Clegg

Company Information

TRIA Bioscience Corporation

1616 Eastlake Avenue East Suite 260
Seattle, WA 98102
   (206) 819-9413
   info@triabio.com
   www.triabio.com
Location: Single
Congr. District: 07
County: King

Phase I

Contract Number: ----------
Start Date: ----    Completed: ----
Phase I year
2018
Phase I Amount
$224,966
Type A and B Influenza viruses cause severe seasonal epidemics and less frequent but more deadly pandemic infections. Vaccination provides the best protection, although serious problems are confronting the global Influenza market. Virus diversity and mutation rates necessitate the annual production of hundreds of millions of vaccines using antiquated egg-based technologies. Compounding this is the risk of choosing the wrong vaccine strain, which leads to sharp drops in efficacy and increased infection rates. New transformational technologies are needed to combat Influenza. The best solution is a universal vaccine that will establish long- term immunity against all genetic strains. This can only be accomplished by constructing vaccines around highly conserved protein sequences common to all viruses. Importantly, these antigens are known and numerous studies indicate that vaccines targeting linear epitopes within 4 viral proteins can be used to induce protective antibodies against both Type A and Type B viruses. TRIA Bioscience is developing a self-assembling peptide nanoparticle vaccine platform that incorporates these and similar linear B cell epitopes directly into synthetic peptides capable of stimulating significant functional antibody responses. The ease of production and formulation of such peptides makes this an ideal technology for mass production. We propose to build a multivalent universal Influenza vaccine that targets these highly conserved epitopes and confers long-lived immunity against multiple Influenza classes and strains. Mice will be immunized with individual peptides to confirm that each epitope induces an antiviral antibody response. The relative potency of each vaccine will be evaluated in mouse challenge studies and multivalent formulations will tested for improved protection against Influenza A and B viruses.

Public Health Relevance Statement:
Narrative Influenza infection is an acute global health issue and new technologies are needed that can maximize vaccine immunogenicity and ease manufacturing constraints. TRIA Biosciences is developing a multivalent universal Flu vaccine using synthetic peptides.

Project Terms:
No Project Terms available.

Phase II

Contract Number: ----------
Start Date: ----    Completed: ----
Phase II year
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Phase II Amount
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