SBIR/STTR Research Award

Prevention of Hearing Loss with Antioxidants and a Vasodilator

Award identifier e0358d8b6bc905ec32117a304c2a84728a5e458ef8b2b227300de46b26485ebeAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$108,465

Program and phase

SBIR · Phase I

Award year

2008

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
OTOMEDICINE, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PHS2007-2
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): More than 30 million Americans are exposed to hazardous sound levels on a regular basis. Of the 28 million Americans who have significant hearing loss, about one-third can be attributed, in part, to noise exposure. Avai lability of an effective treatment that prevents hearing loss in at-risk human populations would improve the quality of life for millions, and decrease healthcare costs for individuals, businesses, and government agencies. OtoMedicine Inc. has identified a proprietary combination of dietary supplements called Auraquell , which is highly effective in preventing permanent noise-induced hearing loss (NIHL) and sensory cell death in a guinea pig model. To efficiently evaluate the efficacy of Auraquell in human s, clinical trials should evaluate prevention of temporary noise-induced hearing loss in human subjects. To justify this clinical paradigm, the Phase I research proposes to demonstrate the therapeutic efficacy of Auraquell in a guinea pig model of tempora ry noise-induced hearing loss. These results will support the three Specific Aims of the Phase II program: (1) determine the plasma concentrations of the active components of Auraquell in guinea pigs that are effective in attenuating temporary noise-induc ed hearing loss, (2) establish an oral dosing paradigm in humans that achieves similar plasma concentrations as those in (1), and (3) evaluate the efficacy of the human oral Auraquell dose in a clinical study designed to measure temporary threshold shift (TTS temporary hearing loss) from exposure to moderate-level music presented via an iPOD personal music player and insert earphones. In Phase III, we will petition the FDA (as specified in 21CFR 101.70) for a health claim and market Auraquell as a safe and efficacious preventative treatment for NIHL.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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