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Published January 19, 2010
Volume 18, Number 1


Roche Molecular Receives FDA Approval for Plasma-Screening Product        
Testing Procedure Can Identify HIV, Hepatitis B, C Viruses


Roche Molecular Systems has recently received FDA approval
for a test  which will help ensure that there is a ready supply of
plasma fordoctors nationwide. 


By Nicole Zaro Stahl
NETWORK Editor


Advances in medical science notwithstanding, researchers have yet to develop a successful substitute for human blood, according to AABB, the Baltimore-based organization that represents blood banks around the world. As a result, blood donation, often referred to as “the gift of life,” plays an incalculable role in the recovery of the almost- five-million Americans whose lives are saved by blood transfusions every year. U.S. hospitals and emergency treatment centers have a need for approximately 40,000 units of blood on a daily basis. With a unit--which measures 450 ml, or just under a pint--being the typical yield from each donor visit, the demand for individual donations approaches 15 million annually.

Fortunately, the nation’s blood supply today is “safer from infectious diseases than it has been at any other time,” the U.S. Food and Drug Administration (FDA) has determined. Improvements in donor screening procedures and the variety of new tests that have emerged over the past few years get the credit for this positive state of affairs.

One of the forces behind the progress is Roche Molecular Diagnostics (RMD), headquartered here in Hacienda. The Pleasanton Research and Development Site accommodates more than 200 scientists and associated R&D staff specializing in infectious disease, human genetics, and oncology programs. Many of these high-powered minds are busy at work in the three-story,135,000-square-foot R&D center that came on line almost two years ago.

Last month, RMD head Daniel O'Day demonstrated the company’s commitment to providing screening tests that “ensure the highest safety of blood and plasma products” in announcing F.D.A. approval for an additional intended use for Roche’s licensed nucleic acid test (NAT): screening pools of plasma that may include donations from up to 96 individuals.

Run on RMD’s automated polymerase chain reaction (PCR) equipment, known as the cobas s 201 system, the new cobas® TaqScreen MPX Test has a significant role to play in reducing the risk of transfusion-transmitted infections. The test can simultaneously detect three critical viruses in human plasma: the human immunodeficiency virus (HIV-1 Group M RNA, HIV-1 Group O RNA , HIV-2 RNA); hepatitis C virus RNA; and hepatitis B virus DNA. In late 2008 the test received U.S. approval for screening plasma specimens from individual blood donors. In 2009, it earned the CE Mark, certification that it meets European Union health requirements, for screening source plasma. Now its expanded use has been approved as well.

“Our multiplex test has been widely adopted and has demonstrated excellent performance in blood centers worldwide,” Day has commented. “We are pleased to introduce the expanded use within the U.S. as we continue to further invest in solutions for this critical industry.” 

RMD is a part of Basel, Switzerland-based Roche, a leader in research-focused healthcare with combined strengths in pharmaceuticals and diagnostics, and the world's largest biotech company with over 80,000 employees worldwide.  For more information about RMD’s blood-screening products and other research, visit http://molecular.roche.com.

 

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