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Development of an in vitro assay as correlate of passive immune protection against botulinum neurotoxin to minimize use of whole animal testing

Award Information
Agency: Department of Defense
Branch: Office for Chemical and Biological Defense
Contract: W81XWH-11-C-0085
Agency Tracking Number: C111-109-0018
Amount: $149,949.00
Phase: Phase I
Program: SBIR
Solicitation Topic Code: CBD11-109
Solicitation Number: 2011.1
Solicitation Year: 2011
Award Year: 2011
Award Start Date (Proposal Award Date): 2011-05-18
Award End Date (Contract End Date): 2012-05-27
Small Business Information
5754 Pacific Center Blvd Suite 204
San Diego, CA -
United States
DUNS: 129852864
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 Eric Ervin
 Vice President R&D - EBS Utah
 (801) 582-0146
Business Contact
 Tracey Wrightson
Title: Director of Operations
Phone: (858) 412-1800
Research Institution

This Small Business Innovation Research Phase I project will develop a non-animal based in-vitro assay for determining the efficacy of Botulinum (BoNT) neutralizing therapeutics; the dual nanopore assay (DNPA). New technologies are currently needed in order to facilitate the development and approval of BoNT vaccines and therapies, and align with the NIH and FDA"s guidance for reducing/replacing the number of vertebrate animals used in medical testing. Currently, the mouse lethality neutralization (MLN) assay is the standard test for determining the efficacy of BoNT neutralizing therapeutics. However, the inherent variability in sensitivity of the MLN assay due to different mouse species, test conditions, and the need to utilize live animal testing severely limit its accuracy and utility. EBS"s DNPA will be capable of monitoring the complete mechanism of all seven BoNT isoforms, making rapid analysis of BoNT neutralizing therapeutics, including complex mixtures, possible.

* Information listed above is at the time of submission. *

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