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2008 | 2007 | 2006 | 2005 | 2004 | 2003 | 2002 Vasogen’s ACCLAIM Trial in Advanced Chronic Heart Failure Reaches Target Number of Endpoint Events Toronto, Ontario - November 14, 2005 Vasogen Inc. (NASDAQ:VSGN; TSX:VAS), a leader in the research and development of technologies targeting the chronic inflammation underlying cardiovascular and other inflammatory conditions, today announced that the pivotal phase III ACCLAIM trial of its Celacade™ technology in patients with advanced chronic heart failure has reached its pre-specified objective of 701 primary endpoint events. Achieving this key objective allows for the 2,400-patient, multi-national ACCLAIM trial to be completed by year-end, with results of the study to be made available following data analysis. In North America and Europe, chronic heart failure affects over ten million people, is associated with more than 600,000 deaths each year, and is the leading cause of hospitalizations in people over the age of 65. “We are very excited to have reached this important milestone in the ACCLAIM trial, as Celacade has the potential to be the first broad spectrum anti-inflammatory strategy to address the high mortality and morbidity risk faced by all heart failure patients,” commented James Young, MD, Chairman of the Division of Medicine at The Cleveland Clinic Foundation, and Global Principal Investigator and Chairman of the Steering Committee for Vasogen’s ACCLAIM trial. “We initiated ACCLAIM based on the results of our phase II trial in which Celacade demonstrated an impressive reduction in the risk of death and hospitalization in advanced chronic heart failure patients and we now look forward to reporting the results of this landmark study.” The double-blind, placebo-controlled ACCLAIM trial, which was designed by an independent steering committee comprising thought leaders in heart failure from around the world, is intended to definitively assess the impact of Vasogen’s Celacade technology on reducing the risk of death and cardiovascular hospitalizations in patients with advanced chronic heart failure and to support regulatory approval and market introduction in North America and Europe. The trial was designed to conclude when a minimum of 701 primary endpoint events, defined as either a death or first cardiovascular hospitalization, has occurred and all patients have been in the study for a minimum of six months. About Heart Failure About Vasogen |
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