SBIR-STTR Award

Novel Imaging Agents To Expand The Clinical Tool Kit For Cance
Award last edited on: 1/26/16

Sponsored Program
SBIR
Awarding Agency
NIH : NCI
Total Award Amount
$249,748
Award Phase
1
Solicitation Topic Code
NCI
Principal Investigator
Stephen Fiacco

Company Information

EvoRx Technologies Inc

129 N Hill Avenue Suite 107
Pasadena, CA 91106
   (626) 765-1951
   info@evorxtechnologies.com
   www.evorxtechnologies.com
Location: Single
Congr. District: 27
County: Los Angeles

Phase I

Contract Number: N43CA130065
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2013
Phase I Amount
$249,748
Targeted molecular imaging of cancer is vital for better personalized medicine, but requires novel imaging agents that recognize key molecular surface cell markers. Her2 is overexpressed in 20-30% of breast cancer and is targeted by Herceptin, yet no molecular imaging agent for Her2 is clinically approved. We propose to use Scanning Unnatural Protease Resistant (SUPR) peptides to develop a novel Her2-specific radiotracer for PET/CT. SUPR peptides show antibody-like affinities, resistance to proteolytic andmetabolic modification, and rapid clearance from systemic circulation, making them ideal imaging agents. First, Anti-Her2 SUPR peptides modified with a near-infrared optical dye will be screened for Her2-specific tumor uptake mice. We will then synthesize[18F]-labeled SUPR peptides to image Her2-overexpressing tumors by PET/CT. EvoRx Technologies will collaborate with the MD Anderson Cancer Center to rapidly translate SUPR peptides into a powerful nuclear imaging tool, advancing the personalized treatmentof breast cancer. PUBLIC HEALTH RELEVANCE

Public Health Relevance:
Molecular imaging can improve clinical choices for breast cancer treatment. We propose to develop more accurate and non-invasive imaging molecules to identify patients who would benefit from targeted cancer therapies. This technology will reduce painful and invasive biopsies and provide physicians with significantly more diagnostic information to personalize breast cancer treatment.

Phase II

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Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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