An FDA advisory panel voted 16-1 (with one panelist abstaining) against recommending approval of Watertown, MA-based Acusphere’s (NASDAQ:[[ticker:ACUS]]) heart imaging agent, citing abnormally low blood pressure and other reported side effects of perflubutane polymer microspheres (Imagify) as concerns, the AP reports. The imaging agent is intended for use in diagnosing heart disease. The FDA is not obligated to follow the guidance of the advisory panel.
Author: Ryan McBride
Ryan is an award-winning business journalist who contributes to our life sciences and technology coverage. He was previously a staff writer for Mass High Tech, a Boston business and technology newspaper, where he and his colleagues won a national business journalism award from the Society of American Business Editors and Writers in 2008. In recent years, he has made regular TV appearances on New England Cable News.
Prior to MHT, Ryan covered the life sciences, technology, and energy sectors for Providence Business News. He graduated with honors from the University of Rhode Island in 2001 with a bachelor’s degree in communications. When he’s not chasing down news, Ryan enjoys mountain biking and skiing in his home state of Vermont.
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