Patient-Clinician Encounter Information Modeling Through Web Based Intelligent 3D Visual Interfaces

Award Information
Agency: Department of Defense
Branch: Office of the Secretary of Defense
Contract: DAMD17-02-C-0005
Agency Tracking Number: O012-0277
Amount: $100,000.00
Phase: Phase I
Program: SBIR
Awards Year: 2001
Solicitation Year: N/A
Solicitation Topic Code: N/A
Solicitation Number: N/A
Small Business Information
ARPHARM BIOTECHNOLOGY, LLC
4801 North Shore Drive, Little Rock, AR, 72118
DUNS: 076883060
HUBZone Owned: N
Woman Owned: N
Socially and Economically Disadvantaged: N
Principal Investigator
 Slaton Fry
 Project Manage
 (501) 758-8500
 krcoleman@safefoods.net
Business Contact
 Kathryn Coleman
Title: Majority Partner
Phone: (501) 663-2383
Email: krcoleman@safefoods.net
Research Institution
N/A
Abstract
Cervical cancer is one of the most common cancers in women worldwide, with about 450,000 new cases diagnosed each year. In the United States, widespread screening (the Pap smear) has reduced mortality by 70% and reduced incidence to approximately 15,000new cases annually. Approximately 35% of U.S. patients will develop advanced, metastatic disease, for which treatment results are poor. Specific strains of human papillomavirus (HPV) are known to represent important risk factors in the development ofcervical cancer. An experimental vaccine has been developed that involves stimulating dendritic cells from the patient by exposure to two marker proteins from specific strains of HPV. The stimulated cells are injected into the patient, which produces animmune response to the tumor. The vaccine depends on having a reliable supply of the two marker proteins. We plan on applying recombinant DNA technology to induce a genetically modified (GM) strain of canola to produce these proteins in seeds. In thisphase, we will develop the methodology for genetically modifying the plants and will prove the presence of E6 and E7 in the seeds. This work will lay the foundation for the eventual development of a commercial route to produce both proteins. The proposedresearch, if successful, will determine if these two proteins can be produced in a system employing green plants as manufacturing units. These data will form the foundation for future Phase II work, which will be directed at developing a commerciallyviable purification process for the two proteins from seed matter. Also, data from growing the GM plants in the greenhouse will be used to provide information for growing the GM plants in the field and for controlling the proper variables so that currentgood manufacturing practices are observed in the field production and purification processes. Phase III research and development will be aimed at scaling the process to enable production of all of the E6 and E7 needed for this particular application.Ultimately, if this project is successful, the production of the two proteins in this manner will make the experimental vaccine for the treatment of cervical cancer widely available. Lastly, the work in this phase will provide data that will be used inthe development of plant systems for the production of a pipeline of therapeutic proteins, which ArPharm Biotechnology intends to commercialize. These proteins, many of which are currently being tested as potential treatments, will be directed towardstreatments of cancers of the reproductive system and for the treatment of sexually transmitted diseases.

* information listed above is at the time of submission.

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