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Sarah Schiltz
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sschiltz@diadexus.com

diaDexus Receives CE Mark Certification for the PLAC® Test

SOUTH SAN FRANCISCO, Calif., December 1, 2008 — diaDexus, Inc. today announced that it received CE Mark approval for the automated format of the PLAC Test for Lp-PLA2. This automated format of the PLAC Test, capable of running on a wide range of clinical chemistry analyzers, was also cleared by the U.S. Food & Drug Administration (FDA) in December 2007. diaDexus also announced the first shipment of the CE Marked PLAC Test to Europe.

The PLAC Test is the only blood test cleared by the FDA to assess risk for both coronary heart disease and ischemic stroke associated with atherosclerosis. The PLAC Test measures lipoprotein-associated phospholipase A2 (Lp-PLA2), a vascular-specific inflammatory enzyme implicated in the formation of rupture-prone plaque. It is plaque rupture and thrombosis, not stenosis, that cause the majority of cardiac events. Clinical research demonstrates that early diagnosis of cardiovascular disease improves the likelihood of preventing these events.

According to Patrick Plewman, president and chief executive officer of diaDexus, CE marking for the automated PLAC Test is another milestone for the company. “Over two million people in the 27 EU Member States die of cardiovascular disease each year; heart disease is the leading cause of death, and stroke is third. Working closely with our distribution partners in the EU, diaDexus is committed to expanding access to the PLAC Test in Europe to help identify individuals at increased risk of suffering a heart attack or stroke,” Plewman said.

“It is well documented that traditional risk factors fail to identify many people at risk for developing cardiovascular disease,” said Professor Wolfgang Koenig, M.D., Department of Internal Medicine II, University of Ulm, Germany. “The PLAC Test provides us with information we’ve never had before about a patient’s risk for coronary heart disease and ischemic stroke helping to determine the best course of treatment to prevent these events from occurring. Lp-PLA2 has similar predictive power for both primary coronary heart disease (CHD) in initially healthy subjects, as well as for recurrent events in those with clinically manifest atherosclerosis.”

A June 2008 supplement to The American Journal of Cardiology published an expert consensus panel recommendation to include testing for Lp-PLA2 as an adjunct to traditional risk factor assessment. The panel of experts recommended that the PLAC Test should be used for patients at moderate or high risk for a heart attack or stroke.

About diaDexus
diaDexus, Inc., a privately held diagnostics company based in South San Francisco, is focused on the development and commercialization of patent-protected in vitro diagnostic products addressing unmet needs in cardiovascular disease. For more information, visit www.plactest.com or www.diaDexus.com.



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January 19-21, 2007
Pacific Lipid Association (PLA) Inaugural Meeting

San Diego , California

*A COMPLIMENTARY PLAC Test WILL BE AVAILABLE AT THE BOOTH

February 7-9, 2007

American Stroke Association (ASA) International Stroke Conference

San Francisco, California

Booth #308

*A COMPLIMENTARY PLAC Test WILL BE AVAILABLE AT THE BOOTH

March 24-27, 2007

American College of Cardiology (ACC) 56th Annual Scientific Session

New Orleans, Louisiana

Booth #1465

*A COMPLIMENTARY PLAC Test WILL BE AVAILABLE AT THE BOOTH

April 13-15, 2007

Northeast Lipid Association (NELA) Annual Scientific Forum

Montreal, Quebec

*A COMPLIMENTARY PLAC Test WILL BE AVAILABLE AT THE BOOTH

April 19-21, 2007

American College of Physicians (ACP) Internal Medicine 2007

San Diego, California

Booth #1815

*A COMPLIMENTARY PLAC Test WILL BE AVAILABLE AT THE BOOTH