SBIR/STTR Research Award
REVERSAL OF 'ANTIGEN-SILENCING' FOR CANCER THERAPY
Award amount
$250,000Program and phase
SBIR · Phase IAward year
2001Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- CYTOCURE, 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: (Applicant's Description)
oxide synthase; iNOS) has been implicated in the pathogenesis of various forms
of inflammation. Chronic inflammation is a known risk factor for
carcinogenesis. There are multiple lines of evidence implicating the
iNOS/peroxynitrite pathway in the pathogenesis of intestinal inflammatory
responses. In this proposal, we present evidence that (1)
mercaptoethylguanidine (MEG), and its dimeric form, guanidinoethyldisulfide
(GED) (lead compounds of the applicants' proprietary mercaptoalkylguanidine
class of compound series) are promising nitric oxide synthase (NOS) inhibitors
with selectivity for the inducible nitric oxide synthase isoform (iNOS), and
with an additional peroxynitrite scavenger activity; and (2) that MEG and GED
are compounds of appropriate therapeutic ratio, suitable for preclinical and
clinical development for various forms of inflammation. These data, combined
with (3) novel preliminary evidence implicating the role of the
peroxynitrite/iNOS related mechanisms in the pathogenesis of intestinal
polyposis lend strong support to the current proposal. The aim of the
proposed project is (1) to perform definitive in vivo studies in murine models
of intestinal polyposis using the min/APC model in order to test whether GED
can slow down or reverse the onset of the polyposis; and (2) to perform
subchronic 90-day toxicity studies with GED in 2 species with the compounds in
order to determine whether they are suitable for indications related to
chronic intestinal inflammation/polyposis. The results of the present
application will permit application for Phase 2 SBIR funding to support:
completion of pre-clinical pharmaceutical testing (in order to complete
advanced toxicity determinations, pathology, stability, pharmacokinetics),
preparation of investigational drug application to the FDA, and a Phase I and
II clinical trials.
PROPOSED COMMERCIAL APPLICATIONS:
The annual anticipated revenues for an effective therapeutic to prevent and treat intestinal polyposis is over $200 million in the US alone.
Technology keywords
Not reported