SBIR/STTR Research Award

Development of a Therapy for Dengue Virus Infection

Award identifier aae68ef4c619b08d0535ec394636f51d7e572765808b13c67952c197f6db037fAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$282,480

Program and phase

SBIR · Phase I

Award year

2009

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Enantigen Therapeutics
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PHS2009-2
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): This is a Phase I proposal to develop a new family of imino sugars, with break through , unprecedented, potency, for the treatment of dengue virus (DENV) infection. There is currently no effective treatment for diseases caused by this virus and both the public health and military need are enormous. The ultimate goal is to have a drug tested in people for safety (Phase I clinical trial) within 3 years. DENV has been shown by us and others to be extremely sensitive to imino sugars in vitro and in vivo. Development of imino sugars has been limited by low potency in vivo, due to the inability to achieve sufficient therapeutic concentrations. Our preliminary study with rationally designed chemical modifications on current lead imino sugars, has led to discovery of a novel family of compounds (PBDNJs) with sub-micromolar EC50s and selectivity indexes of more than 800 against dengue virus infection in tissue culture. These represent the best in this class and potencies are 10-20 times better than has ever been previously achieved, making it realistic to consider effective human use. In this Phase I proposal, before committing to current PBDNJs, we will systematically synthesize and test more imino sugar derivatives following the current path of chemical modification, and select candidates with equal to or better activity and cytotoxicity profile than our current lead, for absorption, distribution, drug metabolism and excretion (ADME) studies. Phase I studies will allow the selection of the 2 or 3 best compounds for advancement into phase II, which will consist of testing for toxicity and efficacy in the DENV animal model, and Phase I clinical trials in humans. Since we are co-inventors of the imino sugar antiviral technology, we are confident of our aggressive time frame. PUBLIC HEALTH RELEVANCE: This is a proposal for the development into a drug of a novel family of imino sugars with breakthrough antiviral activity against dengue virus (DENV). This compound would function through interfering with virion secretion by targeting a host enzyme required for this process, and may be of use by itself or in combination with other potential candidates with different mechanism-of-action to extend efficacy. At the end of the proposed project, the novel imino sugar compound would be ready for large-scale Phase II/III clinical testing with dengue infected patients.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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