SBIR/STTR Research Award

Development of a Small Molecule Inhibitor for EBV Latent Infection

Award identifier 81bafdc9aadd747cd824765fb0a6cd7a5331158f5bee9e9ce90824196b003b5fAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$1,500,000

Program and phase

SBIR · Phase II

Award year

2014

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
VIRONIKA LLC
Proposal award date
2014-06-15
Contract end date
2017-05-31
UEI
F391LAAT74P4
Solicitation number
PA13-234
Topic code
NIAID

Research abstract

DESCRIPTION provided by applicant The goal of this research program is to develop a novel small molecule inhibitor of latent Epstein Barr Virus EBV infection EBV is a ubiquitous gamma herpesvirus that has been classified by the World Health Organization as a human carcinogen Vironika with its consortium partners the Wistar Institute and Fox Chase Chemical Diversity Center Inc will develop a highly specific and potent inhibitor of EBV latency that wil provide an important therapeutic strategy to treat EBV associated diseases Latent infection is associated with multiple human malignancies including Burkittandapos s lymphoma nasopharyngeal carcinomas Hodgkinandapos s lymphoma gastric carcinomas and immunoblastic B cell lymphomaandapos s during immunosuppression Currently no EBV specific therapies exist that target latent infection and therefore it remains impossible to effectively treat or prevent EBV associated disease The latent infection depends on a viral encoded protein which functions in the replication and maintenance of the viral genome Genetic and biological disruption of this protein blocks viral latent infection and EBV dependent B cell growth The binding domain of this protein has been characterized structurally and biochemically and serves as an ideal molecule for targeted small molecule inhibition of EBV infection We have screened over compounds in our primary HTS screen and identified one lead In parallel we have discovered another lead molecule using a fragment based approach These leads have high potency selectivity and wide safety margins In this Phase application we propose to use an iterative process for lead optimization We will synthesize analogues test their efficacy in in viro and cell based assays and monitor their ADME liabilities Lead analogs will then be tested to determine pharmacokinetic properties toxicity and efficacy in a mouse model For each round we will optimize the efficacy and potency of the chemotypes and mitigate toxicity or other liabilities The goal of this Phase project is to identify one pre clinical candidate with which e can perform IND enabling studies to take into Phase first in man clinical trials PUBLIC HEALTH RELEVANCE The research program described in this proposal will reduce the incidence of latent non active infection by Epstein Barr Virus EBV Latent EBV has been classified as a human carcinogen and is associated with nasopharyngeal carcinomas Burkittandapos s lymphoma and Hodgkinandapos s lymphoma The product being developed in this proposal is the first therapeutic small molecule drug that specifically disrupts EBV latent infection

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

9 SBIR/STTR records share this UEI (2009–2022). Reported award amounts total $4,734,680. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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