ADVISORY, Dec. 5, 2013 (GLOBE NEWSWIRE) --
Venaxis, Inc. [APPY], an in vitro diagnostic company focused on obtaining FDA clearance and commercializing its CE Marked APPY1™ Test, a rapid, multiple biomarker-based assay for identifying patients that are at low risk for appendicitis, will visit the NASDAQ MarketSite in Times Square.
In honor of the occasion, Steve Lundy, President and CEO, will ring the Closing Bell to celebrate the company's recent achievements as it advances the APPY1 Test toward potential FDA clearance and expands its commercial footprint in the EU. Venaxis™ remains on track to complete patient enrollment for its pivotal clinical study of the APPY1 Test in the United States at or around the end of 2013.
NASDAQ MarketSite – 4 Times Square – 43rd & Broadway – Broadcast Studio
Friday, December 6, 2013 – 3:45 p.m. to 4:00 p.m. ET
Tiberend Strategic Advisors, Inc.
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Gal 3C/06C 95.05 degrees West
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About Venaxis, Inc. [APPY]:
Venaxis, Inc. is an in vitro diagnostic company focused on the clinical development and commercialization of its CE Marked APPY1 Test, the Company's rapid, protein biomarker-based assay for appendicitis. This unique appendicitis test has projected high sensitivity and negative predictive value and is being developed to aid in the identification of patients at low risk for acute appendicitis, allowing for more conservative patient management. The APPY1 Test is being developed initially for pediatric, adolescent and young adult patients with abdominal pain, as this population is at the highest risk for appendicitis and has the highest risk of long-term health effects associated with CT imaging. While FDA clearance is being sought, an initial launch for the APPY1 Test is ongoing in select European countries. For more information, visit www.venaxis.com.
About NASDAQ OMX Group:
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