Measuring metabolism of C-terminal fragments of amyloid beta in the human central

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$814,440.00
Award Year:
2011
Program:
SBIR
Phase:
Phase II
Contract:
4R44AG034725-02
Agency Tracking Number:
R44AG034725
Solicitation Year:
2011
Solicitation Topic Code:
NIA
Solicitation Number:
PA08-050
Small Business Information
C2N DIAGNOSTICS, LLC
4041 FOREST PARK AVE, SAINT LOUIS, MO, 63108-3213
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
828289210
Principal Investigator:
TIM WEST
(314) 633-1886
twest@c2ndiagnostics.com
Business Contact:
TIM WEST
(314) 633-1886
twest@c2ndiagnostics.com
Research Institution:
Stub




Abstract
DESCRIPTION (provided by applicant): This grant will seek to develop a methodology that will allow us to test whether a promising new class of drugs for Alzheimer's disease is having the desired effect in the human brain. This methodology will allow pharmaceutical companies to make informed decisions about which drugs to advance into late stage clinical trials, and to optimize dosing and administration schedules based on pharmacodynamic response. C2N Diagnostics has licensed the platform technology from Washington University to carry out the company's stable isotope labeling kinetic (SILK) assay. This assay is used to measure production and clearance rates of proteins in the brain. Previously, this methodology has been applied to measuring production and clearance of total A2 from the brain, and evaluating the biologic activity of certain compounds in clinical development for the treatment of Alzheimer's. To measure the biologic activity of an emerging class of compounds, gamma-secretase modulators, we need to be able to measure the production and clearance of the individual A2 isoforms, specifically A2 38, 40 and 42. The experiments proposed in this grant will develop this methodology in Phase I of this grant. In Phase II, the methodology will be applied to asmall patient study. Applying the technology to a proof of concept human study will greatly facilitate commercialization of the technology. Further, this technology will greatly enhance our understanding of how AD metabolism plays a role in the pathogenesis of the disease. PUBLIC HEALTH RELEVANCE: Alzheimer's disease is a growing problem with an estimated 5 million people currently affected in the US. There are currently no disease modifying drugs approved for AD, in part due to a paucity of relevant toolsto measure biologic activity and clinical efficacy for these types of drugs. The proposed experiments are intended to allow C2N to help pharmaceutical companies optimize the quality of their drug development efforts and to expedite bringing promising disease modifying treatments to the clinic.

* information listed above is at the time of submission.

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