Development of an LPA receptor modulator Rx100 as a radioprotectant

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$99,977.00
Award Year:
2008
Program:
SBIR
Phase:
Phase I
Contract:
1R43CA130424-01A1
Award Id:
88871
Agency Tracking Number:
CA130424
Solicitation Year:
n/a
Solicitation Topic Code:
n/a
Solicitation Number:
n/a
Small Business Information
RXBIO, INC., 1325 SUNSET DR, JOHNSON CITY, TN, 37604
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
185698334
Principal Investigator:
() -
Business Contact:
() -
smccool@rxbio.com
Research Institute:
n/a
Abstract
DESCRIPTION (provided by applicant): Bone marrow and gastrointestinal mucosa are highly sensitive to radiation exposure. Radiation-induced damage to bone marrow and the gastrointestinal tract could be lethal in events such as nuclear accidents or radiation terrorism, depending on radiation doses, exposure rate and quality. No truly satisfactory radioprotective drugs are yet available. The phospholipids growth factor lsophosphatidic acid (LPA) is a prosurvival factor acting via LPA receptors. We have synthes ized a LPA receptor modulator Rx100, a partial agonist for LPA1 and LPA3, and a potent agonist for LAP2 receptor. We have proof of principle that Rx100, when applied either orally or subcutaneously, 1 hr before or 3 hrs after radiation exposure effectively reduced radiation-induced lethality to mice. We propose to fully evaluate Rx100 as a radioprotectant and a radiomitigator. Our ultimate goal is to provide a highly efficient medical countermeasure against radiological and nuclear threats, and a potent rad ioprotectant for cancer patients. Research design: Evaluate the efficacy of Rx100 in ameliorating radiation-associated hematopoietic syndrome. (1) We will use a mouse model of whole-body radiation; (2) We will optimize dosing schedules by oral and subcutan eous routes; (3) We will compare all data to decide two final schedules: one for Rx100 administered prior to radiation exposure as a radioprotectant and one as a radiomitigator; (4) We will quantify Rx100-initiated radioprotection by dose-reduction factor (DRF). Methods: (1) whole-body radiation of mice. Conscious mice are subjected to whole-body irradiation using a Cs-137 source at a rate of 4.6 Gy/min. (2) Hematopoietic assay. The primary endpoint is 30 days overall survival. For determining DRF, mice wil l be subjected to graded lethal doses of radiation exposure to generate survival curves for control groups and Rx100-treated groups. DRF will be calculated by probit analysis. PUBLIC HEALTH RELEVANCE: Exposure to radiation could result in fatal damage to b one marrow and the gut. No truly satisfactory radioprotective drugs are available yet. We propose to develop Rx100 into a highly efficient medical countermeasure against radiological and nuclear threats, and a potent radioprotectant for cancer patients.

* information listed above is at the time of submission.

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