Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
INTEGRA BIOSCIENCES AG

Download Mobile App




POC Test Will Directly Target HIV

By LabMedica International staff writers
Posted on 31 Jul 2013
A low-cost, point-of-care (POC) HIV antigen/antibody combination diagnostic device is being developed.

The MBio Diagnostics (Boulder, CO, USA) HIV antigen and antibody assays provided a combined performance that significantly exceeded performance of US Food and Drug Administration (FDA; Silver Spring, MD, USA) approved rapid tests, and provides near equivalence of much more complicated laboratory-based tests. More...
MBio Diagnostics, Inc. has a longstanding collaboration with a team of world-class infectious disease experts at the University of California, San Diego (UCSD; USA). The company will be building on the UCSD group’s extensive clinical expertise in acute HIV infection diagnosis as part of this development program.

The National Institute of Allergy and Infectious Diseases (Bethesda, MD, USA), a division of the National Institutes of Health (NIH), gave MBio Diagnostics a two-year USD 1.4 million award to develop the HIV antigen/antibody combination diagnostic device. The two-year award from the Small Business Innovative Research (SBIR) program will continue work from a Phase I NIH project in which research and development of a POC antigen/antibody combination diagnostic device met or exceeded technical milestones.

Michael J. Lochhead, MBio Diagnostics CTO and grant principal investigator, offered, “HIV infection remains a major public health crisis both in the United States and worldwide. There is an increasing awareness that acutely infected individuals disproportionately contribute to the spread of the disease. These individuals remain the most difficult to identify, as infectivity is highest prior to the appearance of the HIV antibodies that serve as the basis of serological diagnostics. There are currently no FDA-approved POC tests that directly target HIV viral antigens. A major goal of this project is to simplify assay workflow to the point it can be run by minimally trained operators in a variety of healthcare settings. The milestone aim of this project is a portable, integrated system delivered to clinical collaborators that meets FDA clinical laboratory improvement amendments (CLIA) waiver guidance requirements.”

Christopher J. Myatt, founder and CEO of MBio Diagnostics added, “The ability to validate a system using well characterized early HIV infection specimens, and to place such systems in an intended use setting capturing operational and usability feedback with capillary and venous blood samples, will accelerate our pipeline of diagnostic products for tuberculosis, hepatitis C, as well as other indications.”

The MBio system is initially being commercialized to manage treatment of HIV patients from a single drop of blood. The detection system is being developed for a broad menu of applications including multiplex assays and cellular analysis.

Related Links:
The MBio Diagnostics
US Food and Drug Administration
National Institute of Allergy and Infectious Diseases



New
Gold Member
Automated MALDI-TOF MS System
EXS 3000
Collection and Transport System
PurSafe Plus®
Gold Member
Automatic Hematology Analyzer
DH-800 Series
HBV DNA Test
GENERIC HBV VIRAL LOAD VER 2.0
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Hematology

view channel
Image: New evidence shows viscoelastic testing can improve assessment of blood clotting during postpartum hemorrhage (Photo courtesy of 123RF)

Viscoelastic Testing Could Improve Treatment of Maternal Hemorrhage

Postpartum hemorrhage, severe bleeding after childbirth, remains one of the leading causes of maternal mortality worldwide, yet many of these deaths are preventable. Standard care can be hindered by delays... Read more
Copyright © 2000-2025 Globetech Media. All rights reserved.