TearLab Presents Results of Landmark Dry Eye Trial at AAO -- PAAO 2009 Joint Meeting


SAN DIEGO, Oct. 26, 2009 (GLOBE NEWSWIRE) -- OccuLogix, Inc. dba TearLab Corporation (Nasdaq:TEAR) (TSX:TLB) announced that Gary Foulks, MD, FACS, presented the poster, "Osmolarity as a Biomarker for Disease Severity in Mild to Moderate Dry Eye Disease," from the TearLab Osmolarity Core Validation Study today at the 2009 American Academy of Ophthalmology (AAO) and Pan American Ophthalmology (PAAO) joint meeting in San Francisco, California.

Dry Eye Disease and a New Severity Index

Data from this landmark study compares the results of individual clinical evaluations to Dry Eye Disease (DED) severity. Over 300 subjects were evaluated in 10 sites worldwide, and for the first time a comprehensive index has been created to classify patients into Normal, Mild/Moderate or Severe categories using an objective and quantitative analysis.

"DED has traditionally been very difficult to diagnose in early and mild stages due to compensatory mechanisms that are in effect during the early transitory phases of the disease. This difficulty to diagnose early stage disease has long been a confounding problem to clinicians and pharmaceutical companies alike. Data from this study clearly demonstrates that in earlier stages of disease, osmolarity shows a progressive increase with increasing severity," stated Dr. Foulks.

Elias Vamvakas, Chairman and Chief Executive Officer of TearLab Corporation, commented, " We are very excited about the results of this study. The demonstrated accuracy and sensitivity of our lab-on-a-chip technology is a breakthrough that will enable doctors to easily diagnose and effectively manage patients with DED. In addition we believe the test will become the catalyst to effective drug development and appropriate prescription."

The TearLab(TM) Osmolarity System

The TearLab(TM) Osmolarity System uses a novel lab-on-a-chip approach that requires less than 50 nL (nanoliters) of tear fluid in order to measure tear osmolarity. The TearLab(TM) Osmolarity System is a breakthrough test that will enable doctors to easily diagnose and effectively manage patients with Dry Eye Disease. The TearLab(TM) Osmolarity System eliminates the challenges that previously prevented point-of-care osmolarity testing. The TearLab(TM) System can produce a sample-to-answer result in less than 30 seconds and is intended to be technician administered.

Dry Eye Disease

DED is a common condition in which the eye produces insufficient tears, tears with abnormal composition, and/or loses excessive tear to evaporation. The resultant damage to the eye surface increases discomfort and sensitivity to bright light. In its mild to moderate forms, it causes pain and can impact vision and the ability to go about daily activities. In its more severe forms, DED can lead to the permanent loss of vision. DED affects approximately 40 million people in the U.S. and 100 million people worldwide.

About OccuLogix, Inc. dba TearLab Corporation

OccuLogix, Inc. dba TearLab Corporation (www.tearlab.com) is an ophthalmic device company developing and commercializing novel, lab-on-a-chip technologies (integrating one or several laboratory functions on a chip only millimeters in size) that enable eye care practitioners to test for highly sensitive and specific biomarkers in tears at the point-of-care.

Forward-Looking Statements

This press release may contain forward-looking statements. These statements relate to future events and are subject to risks, uncertainties and assumptions about the Company. These statements are only predictions based on our current expectations and projections about future events. You should not place undue reliance on these statements. Actual events or results may differ materially. Many factors may cause our actual results to differ materially from any forward-looking statement, including the factors detailed in our filings with the Securities and Exchange Commission and Canadian securities regulatory authorities, including but not limited to our Forms 10-K and 10-Q. We do not undertake to update any forward-looking statements.



            

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