SBIR/STTR Research Award

Multimodality Neuroimaging of DTI-015 Activity in Giloma

Award identifier 1ba56de00fbb2530d9f5bc07c814700c0e2457dc7e9352e9ee52b8d79321c4dfAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$100,000

Program and phase

SBIR · Phase I

Award year

2001

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
DIRECT THERAPEUTICS, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION: (Verbatim from the Applicant's Abstract) Brain tumors are the second leading cause of cancer-related deaths in children and fourth in middle-aged man. Malignant gliomas remain uniformly fatal underscoring the urgent need for new, more effective treatments. More effective therapies coupled with improved imaging information would provide important opportunities to improve care and individualize treatments. The central hypothesis of this SBIR is that a new formulation of BCNU in absolute ethanol (DTI-015) can be administered locafly to treat experimental gliomas and that the spatial delivery of this therapy can be monitored using MRI for subsequent correlation with therapeutic outcome. The regional distribution of vascular effects following DTI-015 injection in experimental animals will be mapped using the perfusion tracer HMPAO. The regional distribution of DTI-015 may be observed with the use of MR through: 1) local trapping of infused intravascular MR contrast in the affected vascular bed; 2) arterial spin-labeling perfusion imaging; 3) bolus intravascular contrast MR perfusion imaging or 4) diffusion-weighted MRI. The MR-observable parameter that can be used as a surrogate marker for detecting drug delivery will be determined. These results are anticipated to provide the foundation for using SPECT and MR in DTI-015 clinical trials. PROPOSED COMMERCIAL APPLICATION: Current treatments for malignant brain tumors are very ineffective and improvements in mean lifespan has not changed for over 20 years for this patient population. A therapeutic approach proven to extend survival would have a tremendous impact and be a commercially viable product.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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