SBIR/STTR Research Award

Therapeutic UV Disinfection System to Prevent Catheter Related Bloodstream Infections (CRBSIs) in Patients with Peripherally Inserted Central Catheters (PICCs)

Award identifier 1780691db2aa967e271c8b183a2046fcffffef4368bce250bec35c8d71461644Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$2,991,119

Program and phase

SBIR · Phase II

Award year

2023

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
PURACATH MEDICAL INC
Proposal award date
2023-07-06
Contract end date
2026-06-30
UEI
NEL5ZE8ESQ55
Solicitation number
PAR20-129
Topic code
NIAID

Research abstract

Abstract The goal of PuraCath’s Commercial Readiness Pilot is to prepare for commercialization of a therapeutic system for disinfection of a needleless connector for Peripherally Inserted Central Catheters that reduces the risk of intraluminal colonization as a source of catheter-related bloodstream infections. The system uses ultraviolet light to eliminate microbes and biofilm derived from fungi and bacteria by 99.99%, a 4-log reduction, to prevent Catheter Line Associated Bloodstream Infections. We propose to develop a commercialization-ready Firefly™ UV Disinfection System. This system consists of a neutral displacement, straight valve, UV-transmissive, needleless connector; and a handheld device with UV LEDs and sensor technology. In Phase II, PuraCath Medical developed and validated the Firefly™ UV Disinfection System performance. The FDA 510(k) submission process was initiated, and an initial clearance was received for the Firefly Needleless Connector (K203796, cleared July 30, 2021). The Firefly UV Disinfection Handpiece and Charging Station are currently under review with the FDA with clearance for the initial design pending (K213160, application filed November 12, 2021). In this Commercial Readiness Pilot, we will complete the steps needed to support clinical use and commercialization, with four aims: 1) Establish readiness for commercial manufacturing, 2) Prepare for clinical trials, 3) Develop a Quality System, integrate manufacturing partners, and design and prepare training materials and; 4) Develop software to monitor and ensure proper use and compliance. These results will enable us to conduct clinical studies that will support our efficacy claims and provide evidence of the benefit of the system. In parallel, we are seeking Phase IIb support to conduct the clinical trials. The outcome of this entire SBIR program will be a body of clinical evidence to drive adoption of the Firefly™ UV Disinfection System by hospitals. The proposed project will improve scientific knowledge in the UV disinfection space for colonized surfaces and clinical practices for infection control in hospitals and outpatient clinics. Additionally, with the help of this NIH CRP grant we will generate data supporting other UV LED applications for disinfection in hospital settings.

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

5 SBIR/STTR records share this UEI (2011–2023). Reported award amounts total $6,864,496. Reported amounts are not federal obligations.

Phases: Phase II, Phase I

Agencies: Department of Health and Human Services, National Science Foundation

Agency intelligence

Department of Health and Human Services

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