SBIR-STTR Award

Hepatitus B virus polymerase as an antiviral drug target
Award last edited on: 3/28/2002

Sponsored Program
SBIR
Awarding Agency
NIH : NIAID
Total Award Amount
$49,410
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Christopher S Barker

Company Information

Avid Therapeutics Inc

3401 Market Street Suite 300 Un Sci Ctr
Philadelphia, PA 19104
   (215) 386-5220
   N/A
   N/A
Location: Single
Congr. District: 03
County: Philadelphia

Phase I

Contract Number: 1R43AI034348-01
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
1993
Phase I Amount
$49,410
There are 300 million people in the world who are chronically infected with hepatitis B virus (HBV). Available therapies for the elimination of HBV infection often have a transient effect only. These therapies do not specifically target HBV, and this, in part, is a basis for their limited and variable performances. We will seek to develop targeted antiviral drugs with a particular emphasis on HBV. The product of the HBV pol gene has a central role in viral replication. It has a complex of functions which include reverse transcription, RNase H. DNA priming, and DNA synthesis. Such unique and essential functions make it a prime target for prospective anti-HBV drugs. This program proposes to seek pol gene-associated activities in soluble products from host cells transformed with expression vectors that contain appropriate constructs prepared from the HBV pol gene. These enzymatically active peptldes will be used to develop microwell-formatted quantitative assays. Further developments will take these assays into automated high- throughput systems for use in large-scale screening of compounds with prospective inhibitory activity. Such inhibitors, once identified and characterized, will form the bases for the development of targeted anti-HBV drugs.Awardee's statement of the potential commercial applications of the research: The product of the HBV pol gene has a central role in viral replication. It has a complex of functions which include reverse transcription, RNase H. DNA priming, and DNA synthesis. Such unique and essential functions make it a prime target for prospective anti-HBV drugs. Further developments will take these assays into automated high-throughput systems for use in large-scale screening of compounds with prospective inhibitory activity, such inhibitors, once identified and characterized,will form the bases for the development of targeted anti-HBV drugs.National Institute of Allergy and Infectious Diseases (NIAID)

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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