SBIR/STTR Research Award

Rapid, Near-Tranfusion Test for Bacteria in Platelets Units

Award identifier 6c939499d53314156c3974ab8e5b9fd78c9e8a61db90729f632f75f9e352e6f4Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$972,241

Program and phase

SBIR · Phase II

Award year

2016

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
IMMUNETICS, INC.
Proposal award date
2015-12-01
Contract end date
2017-11-30
UEI
Not reported
Solicitation number
PA12-088
Topic code
NHLBI

Research abstract

DESCRIPTION provided by applicant Bacterial contamination of platelets is considered the greatest infectious risk of blood product transfusion today at about in platelet units which is several orders of magnitude greater than that of HIV Bacterial contamination at high levels can lead to severe morbidity or mortality in transfusion recipients The American Association of Blood Banks issued directives in and requiring bacterial testing on all platelet units Two recent studies have demonstrated that current FDA approved culture based methods that test for contamination to days prior to transfusion miss a majority of contaminated units The time elapsed between sampling and actual transfusion and the associated risk of bacterial contamination is a fundamental problem that cannot be addressed by current culture based platelet testing A rapid and sensitive point of issue test for bacterial contamination would overcome this problem by providing an assessment of potential contamination immediately prior to transfusion Such a test would be used by a hospital laboratory close to the point of transfusion or by a transfusion center preparing to ship platelet units to a clinical center A rapid test would ideally require less than min have detection sensitivity of CFU mL or better be fully automated and be comparable in cost to current tests BacTx technology developed by Immunetics for detection of bacterial contamination in platelets employs a unique and innovative assay chemistry capable of rapidly detecting both Gram positive and Gram negative bacteria in platelet units The first generation BacTx Bacterial Detection Kit recently received clearance from FDA CBER as a quality control test for pooled leukocyte reduced whole blood derived platelets but this test is not ideally suited for use as a point of issue test due to its length min and complexity requiring centrifugation and accurate pipetting In the Phase I project we successfully demonstrated feasibility of a simple filter based BacTx assay which is rapid andlt min and highly amenable to automation while maintaining the high sensitivity and specificity of the original BacTx test In Phase II we will optimize and configure the rapid test for automated performance and will design build and evaluate prototype instruments and software to run the test The instrument and software development will be carried out in collaboration with engineering partners who have many years of experience in the development of medical test systems with comparable functionality At the conclusion of Phase II we will have developed and validated an integrated rapid BacTx test system ready for clinical studies aimed at k approval Commercialization of this rapid test will enable a paradigm shift in platelet testing and a significant reduction in the number of bacterially contaminated platelet units transfused into critically ill patients Furthermore adopton of the rapid BacTx test could ultimately lead to a change in policy regarding platelets significantly reducing costs for blood banks by allowing an extension of the storage life of platelet units from to days PUBLIC HEALTH RELEVANCE Bacterial contamination of platelets is considered the greatest infectious risk of blood product transfusion today at about in platelet units which is several orders of magnitude greater than that of HIV We have developed a rapid andlt min point of transfusion screening test for detection of bacterial contamination in platelet units that meets or exceeds FDA guidelines We propose to adapt this test to be run by a simple automated device suitable for operation by non specialized personnel in a transfusion center or hospital laboratory Implementation of this rapid test will prevent severe or fatal septic transfusion reactions and lead to better health outcomes for critically ill patients receiving platelet transfusions

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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