Abbott 
                  Receives FDA Approval for Molecular 
                  Test for Hepatitis C
                  
                 Abbott 
                  Park, Illinois -- May 18, 2011 -- Abbott (NYSE: ABT) announced 
                  today that it has received approval from the U.S. Food and Drug 
                  Administration to market its RealTime PCR (polymerase chain 
                  reaction) test for measuring the viral load of hepatitis C (HCV), 
                  the leading cause of liver cancer in the United States.
Abbott 
                  Park, Illinois -- May 18, 2011 -- Abbott (NYSE: ABT) announced 
                  today that it has received approval from the U.S. Food and Drug 
                  Administration to market its RealTime PCR (polymerase chain 
                  reaction) test for measuring the viral load of hepatitis C (HCV), 
                  the leading cause of liver cancer in the United States.
                  
                  The Abbott RealTime HCV assay, developed for use on the Abbott 
                  m2000 system, is intended for use as an aid in the management 
                  of HCV-infected patients undergoing antiviral therapy. The assay 
                  measures HCV RNA levels at baseline and during treatment and 
                  can be utilized to predict sustained and non-sustained virological 
                  response to HCV therapy. The results from the RealTime HCV assay 
                  must be interpreted within the context of all relevant clinical 
                  and laboratory findings. The Abbott RealTime HCV assay is not 
                  for screening blood, plasma, serum or tissue donors for HCV, 
                  or to be used as a diagnostic test to confirm the presence of 
                  HCV infection.
                  
                  "With the addition of the HCV assay to its automated m2000 
                  system, Abbott is the only molecular diagnostics supplier in 
                  the U.S., to offer viral load assays for HIV, HBV and HCV, and 
                  a combination test for chlamydia and gonorrhea, on a single 
                  molecular platform," said Joseph Jacobs, MD, associate 
                  medical director, Abbott Molecular. "This enables laboratories 
                  to consolidate sexually transmitted and infectious disease testing 
                  to improve workflow and productivity. Also, having a single 
                  manufacturer of these tests provides the clinician with a level 
                  of assurance of consistency and quality when managing patients."
                  
                  The Abbott RealTime HCV test offers precise measurement (quantitation) 
                  of HCV in human plasma or serum. It is a highly sensitive HCV 
                  viral load test and the only one for which the limit of detection 
                  (lowest level of virus that generates a positive result) and 
                  the limit of quantitation (lowest exact viral load measurement) 
                  are the same, 12 IU/mL. This level of sensitivity enables clinicians 
                  to measure very low levels of the HCV virus to gauge success 
                  of antiviral drug treatment for eradicating the infection.
                  
                  "Monitoring HCV RNA levels is important in the management 
                  of the disease with antiviral medications such as interferon 
                  and ribavirin," said Paul Martin, MD, a gastroenterologist 
                  and hepatitis researcher with the Schiff Liver Institute and 
                  Center for Liver Diseases in Miami, and clinical investigator 
                  and consultant for Abbott. "Viral load measurements help 
                  physicians determine whether to begin antiviral therapy, influence 
                  decisions on dosing and therapy duration, and identify drug 
                  resistant strains."
                  
                  "The Abbott RealTime HCV assay detects and measures the 
                  six most common HCV genotypes by targeting an essential, highly 
                  conserved segment of the viral genome," said Stafford O'Kelly, 
                  head of Abbott's molecular diagnostics business. "It is 
                  a highly sensitive molecular assay and offers complete coverage 
                  of all HCV genotypes, as demonstrated in peer reviewed publications."
                  
                  A study published in the June 2009 edition of the Journal 
                  of Clinical Microbiology (Chevaliez, Bouvier-Alias, and 
                  Pawlotski) concluded that "the Abbott m2000 RealTime PCR 
                  system for HCV RNA quantification is sensitive, specific, and 
                  precise; that the results are reproducible; and that the platform's 
                  broad dynamic range of quantification is well suited to HCV 
                  RNA monitoring in the clinical setting."
                  
                  In addition to its HCV in vitro diagnostic products, 
                  Abbott currently has four investigational pharmaceutical compounds 
                  in phase 2 clinical trials for the treatment of HCV, including 
                  a protease inhibitor, two polymerase inhibitors and an NS5A 
                  inhibitor.
                  
                  About the Abbott m2000 System
                  
                   Abbott's 
                  automated molecular diagnostics system, the m2000, utilizes 
                  real-time polymerase chain reaction (PCR) technology for detecting 
                  and monitoring infectious diseases and is designed to provide 
                  clinical laboratories a unique system that fully automates all 
                  of the complex and heavily manual steps often associated with 
                  molecular diagnostics.
Abbott's 
                  automated molecular diagnostics system, the m2000, utilizes 
                  real-time polymerase chain reaction (PCR) technology for detecting 
                  and monitoring infectious diseases and is designed to provide 
                  clinical laboratories a unique system that fully automates all 
                  of the complex and heavily manual steps often associated with 
                  molecular diagnostics.
                  
                  Abbott currently markets the m2000 system and a menu of infectious 
                  disease assays in countries throughout the world.
                  
                  About Abbott Molecular
                  
                  Abbott Molecular, abbottmolecular.com, 
                  is a leader in molecular diagnostics -- the analysis of DNA, 
                  RNA, and proteins at the molecular level. Abbott Molecular's 
                  tests can also detect subtle but key changes in patients' genes 
                  and chromosomes and have the potential for earlier detection 
                  or diagnosis, can influence the selection of appropriate therapies, 
                  and may improve monitoring of disease progression.
                  
                  About Abbott
                  
                  Abbott (NYSE: ABT) is a global, broad-based health care company 
                  devoted to the discovery, development, manufacture and marketing 
                  of pharmaceuticals and medical products, including nutritionals, 
                  devices, and diagnostics. The company employs nearly 90,000 
                  people and markets its products in more than 130 countries.