SBIR/STTR Research Award

Recombinant antigen diagnostics for filoviruses

Award identifier 8a858ced91c5447f72dac5bcc69dd44d34fd3af97af2f147fad1d541d2adbd3dAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$590,176

Program and phase

SBIR · Phase I

Award year

2010

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
CORGENIX MEDICAL CORPORATION
Proposal award date
Not reported
Contract end date
Not reported
UEI
LL3JF6BUDL58
Solicitation number
PHS2010-2
Topic code
NIAID

Research abstract

DESCRIPTION (provided by applicant): Viral hemorrhagic fevers (VHFs) are serious, often fatal, illnesses characterized by high fever, damage to the vascular system and multiorgan failure. Our team has successfully produced prototype Lassa virus ELISA that are based on recombinant proteins rather than on reagents that must be produced in high containment laboratories. Under the proposed SBIR, we will now perform critical steps in the preclinical development of commercial recombinant antigen diagnostics for filoviruses, including development of point-of-care lateral flow assays. In MILESTONE 1, we will identify recombinant filovirus proteins (Ebola (EBOV) and Marburg (MARV)) GP, sGP (EBOV only), NP and VP40 appropriate for immunoassay development and initiate production of monoclonal antibodies (MAbs) to these proteins. In MILESTONE 2, we will develop prototype recombinant IgM-, IgG-, and antigen-capture ELISA and lateral flow diagnostics for filoviruses (EBOV and MARV). In the projected MILESTONE 3, we will optimize the scale up and purification of both recombinant filovirus proteins and MAbs, as well as convert to manufacturing with Quality Assurance (QA)/Quality Control (QC) to provide quantities of recombinant proteins and MAbs sufficient for development and testing of commercial assays. In MILESTONE 4, we will perform field testing or BSL-4 testing of the recombinant filovirus ELISA and lateral flow assays to validate and compare with PCR assays. MILESTONE 5 will involve converting manufacturing of the assays to Good Manufacturing Practices (GMP) with QA/QC. The potential use of VHF agents such as EBOV and MARV filoviruses (both are BSL-4 and NIAID Category A agents) as biological weapons directed against civilian or military targets necessitates development of effective, highly sensitive and specific, easy to use, adaptable, and cost-effective diagnostics for public health laboratories, hospital-based clinical laboratories, and point-of-care use. The impact of EBOV in Africa is considerable, and effective diagnostics against these and related viruses can also provide a very significant public health benefit. PUBLIC HEALTH RELEVANCE: The potential use of VHF agents such as the filoviruses Ebola (EBOV) and Marburg (MARV; both are BSL-4 and NIAID Category A agents) as biological weapons directed against civilian or military targets necessitates development of effective, highly sensitive and specific, easy to use, adaptable, and cost-effective diagnostics for public health laboratories, hospital-based clinical laboratories, and point-of-care use. Under the proposed SBIR we will perform critical steps in preclinical development of commercial recombinant antigen diagnostics for filoviruses, including development of point-of-care lateral flow assays.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

2 SBIR/STTR records share this UEI (2010–2014). Reported award amounts total $3,585,438. Reported amounts are not federal obligations.

Phases: Phase II, Phase I

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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