Acusphere, Inc. (NASDAQ: ACUS) today announced that Dr. Richard
Walovitch, Senior Vice President of Clinical Research, has resigned to
pursue another opportunity. His resignation, effective January 9, 2009,
follows an 11 year career with Acusphere, in which he oversaw the
Company’s clinical trials for its lead product candidate, ImagifyTM
(Perflubutane Polymer Microspheres) for Injectable Suspension, a
cardiovascular drug for the detection of coronary artery disease, which
addresses a potential $2 billion U.S. marketplace.
Said Dr. Walovitch, “I am very proud to have been associated with
Acusphere’s efforts on behalf of Imagify, and our work to demonstrate
its benefits to patients and physicians. As the Company awaits
completion of the review by the U.S. Food and Drug Administration, now
is the right time for me to move to the next phase of my career, and I’m
grateful for the experience of working with my many talented colleagues
at Acusphere.”
Sherri C. Oberg, President and CEO of Acusphere, said, “Rick has made
many significant contributions to Acusphere’s success over the past 11
years, and we greatly appreciate his commitment to seeing this project
through to its final stage. We wish him well in his next venture.”
About Acusphere, Inc.
Acusphere (NASDAQ: ACUS) is a specialty pharmaceutical company that
develops new drugs and improved formulations of existing drugs using its
proprietary microsphere technology. We are focused on developing
proprietary drugs that can offer significant benefits such as improved
safety and efficacy, increased patient compliance, greater ease of use,
expanded indications or reduced cost. Our lead product candidate, ImagifyTM
(Perflubutane Polymer Microspheres) for Injectable Suspension, is a
cardiovascular drug for the detection of coronary artery disease, the
leading cause of death in the United States, for which a New Drug
Application (NDA) was submitted to the U.S. Food & Drug Administration
(FDA) in April 2008 and filed in June 2008. Imagify is designed to
enable ultrasound to compete more effectively with nuclear stress
testing, the leading procedure for detecting coronary artery disease. It
is estimated that more than 10 million procedures are done each year in
the U.S. to detect coronary artery disease, the leading cause of death
in the United States. The Company estimates that the potential annual
U.S. market opportunity for Imagify exceeds $2 billion.