SBIR/STTR Research Award

A Subunit Vaccine Against Acinetobacter Baumannii

Award identifier ad5b218c20db709eb8e438698b6ce3e6ba739266e92bc15d4dfe4ed61b43bf1eAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$288,360

Program and phase

SBIR · Phase I

Award year

2025

Explore This Research Award in CaptureIQ

Research the technology, evaluate the recipient and agency, identify related opportunities, and explore potential follow-on work with CaptureIQ.

Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
BIOLOGICAL MIMETICS, INC.
Proposal award date
2024-12-23
Contract end date
2026-11-30
UEI
LJARDLY9MMK5
Solicitation number
PA23-230
Topic code
NIAID

Research abstract

Project Title: Development of a Novel Vaccine against Multi-Drug Resistant Acinetobacter baumannii Abstract: The escalating threat of Multi-Drug Resistant Acinetobacter baumannii (MDR-AB) represents a significant challenge to global health, underscoring the urgent need for effective preventive measures. This SBIR Phase I project aims to develop a novel vaccine candidate that stimulates immune protection against MDR-AB, addressing a critical gap in our current arsenal against antibiotic-resistant infections. Leveraging a multidisciplinary approach, our project integrates advanced immunological techniques, innovative vaccine formulation strategies, and cutting-edge molecular biology tools. Phase I will focus on (1) identifying and characterizing key immunogenic components of MDR-AB that lead to protective immunity, (2) developing a prototype vaccine formulation, and (3) conducting preliminary in vitro and in vivo evaluations to assess immunogenicity and protective efficacy. Employing a novel approach that enhances antigen selection, we aim to select bacterial proteins that induce a strong and durable immune response. As MDR-AB continues to pose a grave threat to public health, particularly in healthcare settings, the development of an effective vaccine is imperative. Our project not only addresses this urgent need but also has the potential to significantly reduce the incidence of MDR-AB infections, decrease reliance on antibiotics, and reduce the evolution of resistant strains. Successful completion of this Phase I project will lay the groundwork for Phase II studies, including extensive preclinical trials and the optimization of the vaccine formulation for clinical application. Phase I Outcomes: Expected outcomes include the identification of optimal protective subunit candidates, the establishment of a prototype vaccine formulation, and evidence of immunogenicity and efficacy in animal models. These results will provide a solid foundation for further development and testing in subsequent phases, moving us closer to a viable vaccine against MDR-AB.

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

21 SBIR/STTR records share this UEI (2001–2025). Reported award amounts total $15,251,994. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services, Department of Defense, Department of Agriculture

Agency intelligence

Department of Health and Human Services

Back to SBIR/STTR Research Awards

Don't take our word for it. Ask AI about RFPCapture.

See what leading AI assistants have to say about RFPCapture and CaptureIQ.

Gemini opens without a prefilled question. The question is copied to your clipboard when the button works. You can also copy it here:

What is RFPCapture.com and its CaptureIQ platform from Smart Logic AI? How does it help federal contractors discover opportunities, evaluate bid/no-bid decisions, research government contracts, and prepare proposals? How does it compare with other federal capture platforms? Use independent sources where available.