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Organismal Radioprotection Through Pharmacological Quiescence

Award Information

Agency:
Department of Health and Human Services
Branch:
N/A
Award ID:
93444
Program Year/Program:
2009 / SBIR
Agency Tracking Number:
AI084284
Solicitation Year:
N/A
Solicitation Topic Code:
N/A
Solicitation Number:
N/A
Small Business Information
G1 THERAPEUTICS, INC.
450 WEST DR, CB 7295 CHAPEL HILL, NC -
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Woman-Owned: No
Minority-Owned: No
HUBZone-Owned: No
 
Phase 1
Fiscal Year: 2009
Title: Organismal Radioprotection Through Pharmacological Quiescence
Agency: HHS
Contract: 1R43AI084284-01
Award Amount: $692,326.00
 

Abstract:

DESCRIPTION (provided by applicant): Hematologic toxicity is a principal cause of morbidity and mortality after exposure to ionizing radiation (IR). G-Zero Therapeutics, with operations in the Research Triangle Park, North Carolina, has developed a nov el approach to mitigating the hematologic toxicity of total body irradiation (TBI). This approach relies on the administration of novel, orally bioavailable small molecule kinase inhibitors around the time of exposure to TBI. These compounds in turn induce pharmacological quiescence (PQ) of the early hematopoietic stem and progenitor cells (HSPC) through the inhibition of cyclin dependent kinases (CDK's) which govern the G1-S transition of the cell cycle. As quiescent cells are resistant to IR, PQ enhances the per cell survival of HSPC by augmenting the repair of DNA damage post-TBI. This enhanced survival of HSPC in turn translates into markedly reduced acute hematologic toxicity. G-Zero has shown in mice that the PQ approach can significantly boost the tol erated dose of IR when administered at the time of TBI (dose modifying factor gt 1.3). Additionally, CDK inhibitor administered 20 hours after TBI still affords significant radioprotection with enhanced animal survival, and we anticipate that time of admin istration can be extended to more than 24 hours post exposure. As little as a single oral dose of kinase inhibitor affords radioprotection, enhancing survival and protecting all blood lineages including red cells, platelets, granulocytes and lymphocytes. G -Zero has licensed broad intellectual property surrounding the use of PQ for radioprotection. In this proposal, we seek to extend these results in three specific aims. In aim 1, we will test several additional CDK small molecule inhibitors with differing p harmacokinetics in vitro and in vivo to identify the optimal dosing schedule for maximal radioprotection. In aim 2, we will perform extensive characterization in rodents of the pharmacology and toxicology of the most promising CDK inhibitors identified in aim 1. In aim 3, we will additionally determine the ability of PQ to afford protection against the long-term sequelae of peri-lethal doses of IR. We believe these Phase I studies will position G-Zero to begin primate studies of CDK inhibitors in Phase II. It is our expectation that this work will lead to a simple and non-toxic pill that will enhance survival when taken up to 24 hours after a peri-lethal IR exposure that could occur as a result of nuclear accident or radiological attack. PUBLIC HEALTH RELEVA NCE: Exposure to radiation from terrorist attack and resulting toxicity is an imminent threat to the American public and military. Hematological toxicity through radiation-induced DNA damage of blood-producing cells of the bone marrow is a severe lethal co nsequence of radiation exposure of humans. G-Zero Therapeutics is developing drugs which can be stockpiled and easily administered following such an attack to protect the bone marrow from the damaging effects of radiation.

Principal Investigator:

John S. Chant

Business Contact:

John S. Chant
Small Business Information at Submission:

G-ZERO THERAPEUTICS, INC.
G-ZERO THERAPEUTICS, INC. 450 WEST DR, CB 7295 CHAPEL HILL, NC 27599

EIN/Tax ID: 126364818
DUNS: N/A
Number of Employees: N/A
Woman-Owned: No
Minority-Owned: No
HUBZone-Owned: No