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Biovista and Cempra Pharmaceuticals enter agreement for macrolide clinical trial design support studies

On September 30, 2008 Chapel Hill, NC and Charlottesville, VA, Cempra Pharmaceuticals, Inc., and Biovista, Inc., announced that they have entered into a research agreement to systematically identify and profile adverse event associations for members of the macrolide drug class. The data generated will be used to better understand the unique benefit/risk characteristics of this important group of antimicrobial drugs, thereby helping to adapt and optimize future clinical trial designs.

"This collaboration with Biovista is a significant step forward in understanding macrolide safety profiles in a way that will help us further our clinical development plans, and ultimately further our goal to bring much-needed antimicrobial and therapeutic drugs to market" said Prabha Fernandes, president and CEO of Cempra.

Read more: http://www.biovista.com/news.php?article_id=125



 
 
 
 

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