SBIR-STTR Award

Defining T cell epitopes in Dengue virus infection
Award last edited on: 12/24/14

Sponsored Program
SBIR
Awarding Agency
NIH : NIAID
Total Award Amount
$3,574,004
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Ramila Philip

Company Information

Immunotope Inc (AKA: Immunotope Diagnostics Inc)

3805 Old Easton Road
Doylestown, PA 18901
   (215) 253-4180
   info@immunotope.com
   www.immunotope.com
Location: Multiple
Congr. District: 01
County: Bucks

Phase I

Contract Number: 1R43AI062177-01A2
Start Date: 6/1/07    Completed: 5/31/10
Phase I year
2007
Phase I Amount
$299,998
Dengue Fever (DF) and Dengue Hemorrhagic Fever (DHF) are significant global public health problems and understanding the overall immune response to infection will contribute to appropriate management of the disease and its potentially severe complications. Live attenuated and subunit vaccine candidates induce primarily an antibody response to the virus, which is not only ineffective, but potentially deleterious. Currently, there are no available tools to assess the protective T cell responses during infection or post vaccination. The primary objective of this project is to create new informational and diagnostic tools to characterize T cell immunity in DV infection for vaccine validation and potentially develop new, effective and protective vaccine strategies.

Phase II

Contract Number: 5R43AI062177-02
Start Date: 6/1/07    Completed: 5/31/09
Phase II year
2008
(last award dollars: 2014)
Phase II Amount
$3,274,006

Dengue Fever (DF) and Dengue Hemorrhagic Fever (DHF) are significant global public health problems and understanding the overall immune response to infection will contribute to appropriate management of the disease and its potentially severe complications. Live attenuated and subunit vaccine candidates induce primarily an antibody response to the virus, which is not only ineffective, but potentially deleterious. Currently, there are no available tools to assess the protective T cell responses during infection or post vaccination. The primary objective of this project is to create new informational and diagnostic tools to characterize T cell immunity in DV infection for vaccine validation and potentially develop new, effective and protective vaccine strategies.

Public Health Relevance:
This Public Health Relevance is not available.

Thesaurus Terms:
Cell, Dengue Virus, Infection Active Immunization, Antibody, Antigen, Arm, Base, Blood, Clinical Trial Phase I, Dendritic Cell, Dengue, Element, Genetics, Genome, Helper T Lymphocyte, Hemorrhagic Fever, Histocompatibility, Human, Hyperthermia, Identity, Immune Response, Immunity, Information System, Insight, Lymphocyte, Major Histocompatibility Complex, Nucleic Acid Sequence, Pathology, Peptide, Protein, Public Health, Role, Serotyping, Vaccine, Vaccine Development, Virus