SBIR-STTR Award

Test To Predict Effectiveness Of Docetaxel Treatment
Award last edited on: 1/30/14

Sponsored Program
SBIR
Awarding Agency
NIH
Total Award Amount
$299,359
Award Phase
1
Solicitation Topic Code
-----

Principal Investigator
Carol Swartz

Company Information

Integrated Laboratory Systems LLC (AKA: Rao Enterprises~ILS)

601 Keystone Park Drive Suite 200
Morrisville, NC 27560
   (919) 281-1110
   tkrao@ils-inc.com
   www.ils-inc.com
Location: Multiple
Congr. District: 04
County: Durham

Phase I

Contract Number: 261201300035C-0-0-1
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2013
Phase I Amount
$299,359
The overall goal of this project is to develop better screening methods to provide castration-resistant prostate cancer patients with more appropriate chemotherapeutic agents. The focus of Objective 1 is the development and validation of a CYP1 81 *3 genotype assay using a PCR based Taqman allelic discrimination technique suitable for eventual use in a GLP/CLIA-certified environment. The assay will determine the patient's CYP1 81 genotype from a blood sample and will provide a rapid prognostic tool to predict survival rate and propensity to respond to Docetaxel or similar agents. Studies outlined in Objective 2 will examine mechanisms of CYP1 81-mediated effects on Docetaxel chemotherapy, emphasizing the interaction of estrogen and its metabolites with Docetaxel. Impacts on cellular health status will be assessed by measuring oxidative stress and by examining apoptosis/necrosis, relative cell survival, influence on cell cycle and micronuclei formation using a multiplex flow cytometry-based assay. Effects on microtubules will be assessed using an assay measuring tubulin polymerization within the cell. Gene expression profiling will be used to assess mechanisms of toxicity known to be driven by mitotic spindle poisons like Docetaxel. The ultimate goal (Phase II) is to establish a cellular-based assay to use as a rapid screen for testing potential candidate drugs.

Project Terms:
Apoptosis; base; Binding (Molecular Function); Biological Assay; Biological Availability; Blood specimen; Cancer Patient; castration resistant prostate cancer; Cell Cycle; Cell Survival; Cells; chemotherapeutic agent; chemotherapy; Development; Diagnostic; Discrimination (Psychology); docetaxel; drug candidate; Effectiveness; Environment; Estradiol; Estrogens; Flow Cytometry; Gene Expression Profiling; Genotype; Goals; Health Status; Human; Measures; Mediating; Methods; micronucleus; Microtubules; Mitotic spindle; Necrosis; Oxidative Stress; Patients; Phase; Poisons; polymerization; prognostic; Quinones; Relative (related person); screening; Survival Rate; Techniques; Testing; tool; Toxic effect; Tubulin; Validation

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
----
Phase II Amount
----