SBIR-STTR Award

Screen for Compounds with Affinity for HBV RNA
Award last edited on: 3/11/21

Sponsored Program
SBIR
Awarding Agency
NIH : NIAID
Total Award Amount
$837,852
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Jaime E Arenas

Company Information

Kinetix Pharmaceuticals Inc

200 Boston Avenue Suite 3000
Medford, MA 02155
   (781) 391-7577
   N/A
   www.kinetixpharm.com
Location: Single
Congr. District: 05
County: Middlesex

Phase I

Contract Number: 1R43AI038766-01
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
1995
Phase I Amount
$100,000
The creation of a high throughput screen for small molecule ligands of specific RNAs is proposed. Such a method will have tremendous potential for identifying novel classes of drugs. Most viruses, for example, encode multiple, complex RNAs that are essential for replication and that are appropriate targets for a high throughput affinity screen. In the first phase of the project, a series of small molecules with established affinity for a given nucleic acid will be used as model systems to prove the principle of the assay. Based on the success of these model systems, a high throughput assay for Hepatitis B virus will be established. In the second phase of the project, a library of small molecules will be tested for affinity to Hepatitis B RNAs. Small molecule ligands identified in the high throughput affinity screen will be tested for biological activity in the slower, more cumbersome secondary bioassays. In addition to its use against HBV, the RNA affinity screen can be used to identify novel therapeutics for the treatment of other viral infections and for the treatment of cell-based diseases by providing a means to identify small molecules that regulate the translation or stability of specific cellular mRNAs. PROPOSED COMMERCIAL APPLICATION: There are few effective antiviral therapies. It is estimated, for example, that over 200 million people are infected with Hepatitis B virus (HBV). This virus can cause chronic infections of the liver, leading to cirrhosis, cancer and death. At present, there is no fully efficacious treatment for the disease. Novel treatments that reduce the morbidity and mortality of such infections can be identified by the proposed research program and would therefore have tremendous commercial potential

Phase II

Contract Number: 2R44AI038766-02A1
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
1997
(last award dollars: 1998)
Phase II Amount
$737,852

Many viral transcripts contain structured RNA elements that regulate critical viral functions through RNA/protein interactions. The goal of this research is the discovery of novel small non-oligonucleotide compounds that inhibit the replication of the human hepatitis B virus (HBV) by binding to specific RNA structures of the HBV pregenome. In phase I of this program, a novel high throughput assay to Screen for Compounds with Affinity for Nucleic acid targets (SCAN) was developed. In Phase II, SCAN will be used to screen compound libraries and natural product collections for compounds that specifically bind to a structured RNA element of HBV. Compounds identified in the screen will be tested for specificity in secondary assays including heterologous-target SCAN assays, translation, and other assays. Compounds with specific affinity for the target RNA will be tested for toxicity in tissue culture and non-toxic compounds will be assayed for inhibition of HBV replication in 2.215 cells. Compounds with antiviral activity will be improved by structure activity relationship (SAR) studies and combinatorial chemistry. In phase III the lead compounds will be tested in animal models (woodchucks) and further improved by medicinal chemistry. PROPOSED COMMERCIAL APPLICATION: The ultimate objetive of this program is to develop effective therapeutic drugs for treatment of HBV infections. Nearly 300,3000 Americans are infected with HBV each year, however no effective antiviral therapy is available to treat these cases. Development of a new class of antiviral drugs that inhibit replication of HBV represents a major contribution to medicine and an excellent commercial opportunity