SBIR/STTR Research Award

Rapid, Point-of-Need Diagnostic for Sexually Transmitted Infections

Award identifier d4628b27242b6a69f3269fd811e611aba4e5624e92bc5288af2815e2d8ba7379Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$297,596

Program and phase

SBIR · Phase I

Award year

2021

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
GODX INC
Proposal award date
2021-04-23
Contract end date
2022-03-31
UEI
FZPKPXA6S8L8
Solicitation number
PA20-260
Topic code
NIAID

Research abstract

Project Summary Over 370 million people worldwide are infected with the sexually transmitted infections (STIs) chlamydia, gonorrhea, and trichomoniasis each year. While treatable, delayed treatment can have serious health problems, including infertility, disseminated infection, and pregnancy complications. Since fewer than half of at-risk individuals are screened for these common STIs, it is necessary to destigmatize STI testing and bring rapid point-of-care STI diagnostics to the developed and especially to the developing world, where over 75% of STI cases are thought to occur. Current nucleic acid-based STI tests offer optimal sensitivity and specificity but require laboratory infrastructure (electricity, refrigeration, and trained laboratory technicians) that is largely lacking where these STIs are most prevalent. These tests take days to return a result, which can result in loss of patient to follow-up and treatment. In addition, these tests fail to track the occurrence of antibiotic-resistant gonorrhea. With increases in azithromycin and ciprofloxacin resistance, and more frequent reports of cephalosporin resistance, multidrug- resistant gonorrhea could become a serious threat to global health, necessitating susceptibility testing and antibiotic stewardship. In this SBIR project, GoDx, Inc. proposes to develop a rapid, hand-held, low-cost, and sensitive point-of-care diagnostic to deliver rapid STI test results, which would simplify screening and allow for immediate treatment at the initial visit. To develop a rapid test for chlamydia, gonorrhea, and trichomoniasis, we will focus on innovations to integrate nucleic acid extraction, amplification, and detection to develop and test a prototype device by the end of Phase II. Our easy-to-use sample preparation device would require fewer than three user steps to purify nucleic acids for downstream detection. We will also reach benchmarks for the sensitive and specific amplification of genetic markers in Neisseria gonorrhoeae, Chlamydia trachomatis, and Trichomonas vaginalis using an isothermal amplification technique followed by lateral flow detection. Our test will also amplify genetic predictors of antibiotic susceptibility to aid in the tracking and treatment of antibiotic resistant gonorrhea. Finally, we will integrate our assays into a test device delivering both STI and AMR test results in 30 minutes, with performance on par with laboratory-based STI tests. Our diagnostic tool will be simple and low-cost, making it ideal for use in the developing world where laboratory infrastructure is lacking, affordable for better screening programs worldwide, and easy enough for eventual in-home testing.Project Narrative We are developing a rapid, low-cost, handheld, point-of-care diagnostic device for the detection of the three most common, treatable sexually transmitted infections STI: chlamydia, gonorrhea, and trichomoniasis which infect over 370 million people worldwide each year. With our rapid, easy-to-use test, healthcare providers and patients can receive results in thirty minutes at the clinicians’ office, greatly simplifying and increasing STI screening and treatment to prevent patient loss to follow-up, minimize spread, and reduce additional health risks associated with STIs, such as birth complications, infertility, and pelvic inflammatory disease. Our test will also include a rapid, molecular screening test for antibiotic susceptibility in Neisseria gonorrhea to aid in the selection of proper treatment, monitor the occurrence of antibiotic resistance, and help curb the spread of multi-drug resistant gonorrhea.

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

7 SBIR/STTR records share this UEI (2017–2025). Reported award amounts total $7,707,842. Reported amounts are not federal obligations.

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

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

Agency intelligence

Department of Health and Human Services

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