Discovery and Development of Anti-Diabetic Drugs.

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$2,905,013.00
Award Year:
2011
Program:
SBIR
Phase:
Phase II
Contract:
2R44DK064497-04A1
Award Id:
n/a
Agency Tracking Number:
R44DK064497
Solicitation Year:
2011
Solicitation Topic Code:
NIDDK
Solicitation Number:
PA10-050
Small Business Information
16800 W 12 MILE RD, STE 201, SOUTHFIELD, MI, -
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
611659819
Principal Investigator:
GERARD HOUSEY
(248) 663-7000
GHousey@housey.com
Business Contact:
GERARD HOUSEY
(248) 663-7000
GHousey@housey.com
Research Institution:
Stub




Abstract
DESCRIPTION (provided by applicant): This is a Resubmission of an NIH Phase II SBIR Renewal Application directed towards developing and optimizing compounds that are capable of stimulating IRS2 foundation for the treatment of Type II diabetes. If successful, such compounds may also be useful for the treatment of a subset of patients with Type I diabetes as well. The overall goal of this proposal is to engage in lead optimization studies of new molecular entities already identified by HPRL scientists that activate the IRS2-branch of the insulin signal transduction cascade in mammalian cells. The NIH SBIR funding support will be used to focus research at Housey Pharmaceutical Research Laboratories (hereinafter HPRL ) to further develop for future commercialization initial discoveries made in the laboratory of Dr. Morris White at the Children's Hospital of Boston, Harvard Medical School, and investigators at the Joslin Diabetes Center. These discoveries have been licensed to HPRL for therapeutic applications.Compounds that activate the IRS2-branch of the insulin-mediated signal transduction cascade have been identified by HPRL as a result of a high throughput screen (HTS) using a target-protein specific cell-based assay system. A subset of these compounds exhibit substantial ability to stimulate cell growth in an IRS2- specific manner. A selected group of such compounds will undergo testing in rodent and human 2-cells together with both in-vitro and in-vivo lead optimization studies in mice. Following successful completion of these studies, a small number of novel, lead-optimized new molecular entities should emerge which may be suitable for advancement into formal preclinical investigational new drug (IND) studies for the treatment of patients with Type II diabetes. HPRL is a fully functional chemical and biological research laboratory that is equipped for modern molecular and cell biological studies, including high throughput screening. Support through the SBIR Phase II Renewal Grant mechanism provides the opportunity to utilize the infrastructure at HPRL for novel and creative projects at the cutting edge of drug discovery and design. Since diabetes is a major disease of substantial proportions world-wide, pharmaceutical products and licensable technologies developed by HPRL will have substantial market opportunities. PUBLIC HEALTH RELEVANCE: Discovery and Development of Anti-Diabetic Drugs.

* information listed above is at the time of submission.

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