ATLANTA, GA -- (Marketwire) -- 09/10/08 -- AtheroGenics, Inc. (NASDAQ: AGIX), a
pharmaceutical company focused on the treatment of chronic inflammatory
diseases, today announced that it has restructured its Board of Directors
to reduce the number of directors from ten to six in order to better align
the size of its Board with the current needs of the Company. Remaining on
the Board will be:
Michael A. Henos Chairman of the Board, AtheroGenics, Inc.
Managing Partner, Alliance Technology
Ventures, L.P.
R. Wayne Alexander, M.D., Ph.D. Chairman, Department of Medicine
Emory University School of Medicine
Samuel L. Barker, Ph.D. Founder, Clearview Projects, Inc.
Vaughn D. Bryson Retired President and Chief Executive
Officer Eli Lilly and Company
Margaret E. Grayson President, Coalescent Technologies
Russell Medford, M.D., Ph.D. President and Chief Executive Officer,
AtheroGenics, Inc.
"We believe that the new AtheroGenics' Board continues to provide the
expertise and experience to guide our Company going forward and to maximize
value for all of our varied stakeholders," said Michael A. Henos, Chairman
of the AtheroGenics Board of Directors.
In connection with the Board restructuring, David Bearman, T. Forcht Dagi,
M.D., Arthur M. Pappas and William A. Scott, Ph.D., resigned from the Board
of Directors. Mr. Henos commented, "We want to thank the departing Board
members for their hard work and contributions to the Company."
About AtheroGenics
AtheroGenics is focused on the discovery, development and commercialization
of novel drugs for the treatment of chronic inflammatory diseases,
including diabetes and coronary heart disease (atherosclerosis). The
Company's lead antioxidant and anti-inflammatory drug candidate, AGI-1067,
is being studied for the treatment of diabetes and has completed a Phase 3
clinical trial known as ANDES (AGI-1067 as a Novel Anti-Diabetic Agent
Evaluation Study). In addition, the Company has other clinical and
preclinical anti-inflammatory compounds, including AGI-1096, an oral agent
for the prevention of organ transplant rejection. For more information
about AtheroGenics, please visit http://www.atherogenics.com.