SBIR/STTR Research Award

HI-443 AS A POTENT ANTI-HIV AGENT

Award identifier ae7de0146dde60ec1e42f480b023683533435cf5a0a4a77d5a46486877c561d2Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$100,000

Program and phase

SBIR · Phase I

Award year

2002

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
PARADIGM PHARMACEUTICALS, LLC
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Combination antiretroviral therapy has become the standard of care for patients with human immunodeficiency virus (HIV) infection in the United States. Unfortunately, emergence of drug resistance hampers the long-term success of anti-retroviral treatment regimens. HI-443 is a rationally designed novel anti-HIV compound with potent activity against NNRTI-resistant HIV- 1. (US Patent Serial Number: 6,124,324). The primary goal of our ongoing research is to establish effective methods aimed at improving its oral bioavailability and develop a clinically applicable solid dosage formulation of HI-443. Recently, we developed 3 candidate formulations of HI-443 with good oral bioavailability. We are now proposing studies aimed at evaluating the toxicity profile of these 3 formulations in mice and examining their anti-HIV activity in a SCID mouse model of human AIDS. Under SPECIFIC AIM 1, we will study the toxicity profile of HI-443-F1, HI-443-F2, and HI-443-F3 in mice. We hypothesize that none of the 3 formulations of HI-443 will cause acute, subacute, or chronic toxicity at the proposed dose levels. Under SPECIFIC AIM 2, we will study the in vivo anti-HIV activity of HI-443-F1, HI-443-F2, and HI-443-F3 in a S C D mouse model of human AIDS. We hypothesize that HI-443-F3 will exhibit potent anti-HIV activity in Hu-PBL-SCID mice at nontoxic dose levels. After completion of this Phase I project, we will propose additional preclinical toxicity, pharmacokinetics, and efficacy studies in a Phase II application. The successful accomplishment of the goals may provide the basis for a new treatment strategy for multidrug resistant HIV-1.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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