SBIR-STTR Award

A High Accuracy Point-of-Care Chlamydia trachomatis Test
Award last edited on: 7/8/04

Sponsored Program
SBIR
Awarding Agency
NIH : NIAID
Total Award Amount
$133,750
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Michael K Helms

Company Information

Quidel Corporation

9975 Summers Ridge Road
San Diego, CA 92121
   (858) 552-1100
   ir@quidel.com
   www.quidel.com
Location: Single
Congr. District: 52
County: San Diego

Phase I

Contract Number: 1R43AI058576-01A1
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2004
Phase I Amount
$133,750
Urogenital disease caused by Chlamydia trachomatis (Ct) is a major public health problem affecting 3-4 million people in the U.S. and over 100 million worldwide annually. Sequelae include urethritis, cervicitis, salpingitis (which can lead to infertility in women), pelvic inflammatory disease, adverse pregnancy outcomes (e.g. abortion, still birth or premature birth), and epididymitis (which can lead to infertility in men), as well as being a risk factor for HIV infection. Chlamydial infections are asymptomatic in up to 70% of women and 50% of men, thus delaying treatment and facilitating transmission. This asymptomatic feature coupled with the ease and efficacy of treatment (e.g. a single dose of azithromycin) places the burden for disease management on diagnosis. Furthermore, a persistent and unmet need exists for rapid, accurate, cost effective and simple (RACES format) diagnostic tests for Ct due to patient noncompliance with treatment and delays in providing treatment to infected patients. Currently marketed point-of-care (POC) Ct tests are rapid, but less sensitive than the more complex, slow and expensive laboratory methods such as cell culture and nucleic acid amplification tests (NAAT). To improve sensitivity without sacrificing specificity, the key challenge, we propose novel and proprietary methods that will provide enhanced sensitivity and reduced background signal, therefore maintaining specificity. The sensitivity enhancement will be assessed by comparison to gold standard tests including cell culture and a NAAT. We hypothesize that the proposed test system will increase testing accuracy while adding the speed and simplicity necessary for widespread POC clinical utilization. The resulting enhanced accuracy Ct POC test is directly relevant to the goal of improving diagnosis of infectious diseases stated by organizations such as the National Institute of Allergy and Infectious Diseases, the Bill and Melinda Gates Foundation and the World Health Organization. Furthermore the novel aspects of the test system are expected to result in significant intellectual property rights for the company.

Thesaurus Terms:
Chlamydia trachomatis, communicable disease diagnosis, diagnosis design /evaluation, diagnosis quality /standard, rapid diagnosis clinical chemistry, reproductive system disorder diagnosis, sexually transmitted disease enzyme linked immunosorbent assay, nucleic acid amplification technique, tissue /cell culture

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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