SBIR/STTR Research Award

Point-of-Care Rapid RNA test for Zika

Award identifier ca680b3a07cdf5856b0a8335b2f4da51c516c8e435619ac6c9fcd44faf93e235Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$999,916

Program and phase

SBIR · Phase II – Direct to Phase II

Award year

2021

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
CROSSLIFE TECHNOLOGIES INC.
Proposal award date
2021-01-15
Contract end date
2022-12-31
UEI
LFE6DJ6KL4E5
Solicitation number
PA19-272
Topic code
100

Research abstract

Point-of-Care Rapid RNA test for Zika CrossLife Technologies Inc. Project Summary/Abstract We aim to develop a rapid point-of-test that detects ZIKV at the point-of-need in andlt; 30 minutes and is appropriate for non-laboratory settings and non-technical personnel. Our proprietary test exploits a novel probe reaction chemistry that allows multiplexed detection of DNA or RNA without sample purification, making it operable as a simple, hand-held test. Patient samples to be input directly into the device without pre- processing and a disposable cartridge carry out amplification of all targets and reports visible results that can be read by eye. We have demonstrated the feasibility of a novel and simple detection of ZIKV using TARA (Templated Assisted Rapid Assay). The key goals of the Phase 2 project are to 1) develop and evaluate automated paper strip device and to 2) validate it using clinical samples. We will evaluate the automated paper strip device using 200 samples from a Navy-IRB approved protocol through our CRADA collaboration with U.S. Naval Medical Research Center and the U.S. Naval Medical Research Unit SIX. We expect a sensitivity (andgt;90%) and specificity (andgt;90%) to the qRT-PCR data on the same samples. The successful achievement of 1) time to result andlt; 30 min, 2) sensitivity andgt; 90%, specificity andgt; 90% and LOD andlt; 500 copies/test, 3) andgt; 90% user feedback on ease of use need for CLIA waiver, 4) requires no instrumentation, power source, or refrigeration of reagents, and 5) quantitative criteria for measuring the outcome of each task are exceeds or equivalent to the RT-PCR molecular test.Point-of-Care Rapid RNA test for Zika CrossLife Technologies, Inc. RESEARCH andamp; RELATED Other Project Information Narrative The rapid spread of Zika virus through the Americas, together with the connection of infection with microcephaly and Guillain-Barré syndrome, have driven this previously overlooked virus into the spotlight. The World Health Organization (WHO) predicts almost four million people could be infected with Zika virus in the Americas in the year 2016.

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

18 SBIR/STTR records share this UEI (2015–2023). Reported award amounts total $12,579,180. Reported amounts are not federal obligations.

Phases: Phase I, Phase II, Phase II – Direct to Phase II

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

Agency intelligence

Department of Health and Human Services

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