Michael J. LaBarre , Ph.D., Vice President, Product Development and Regulatory Affairs

Dr. LaBarre brings to Halozyme strong expertise in chemistry, manufacturing and controls (CMC) and more than 20 years of experience across all aspects of biopharmaceutical research and development. Dr. LaBarre joined Halozyme in 2008. He is responsible for product development and regulatory affairs and is the lead expert on Halozyme’s ENHANZE® drug delivery technology.


Prior to Halozyme, he served as Vice President of Product Development at Paramount BioSciences, LLC, where he led the CMC efforts for all of the product development programs within Paramount’s portfolio companies. Prior to joining Paramount, Dr. LaBarre served in various research and development positions from 1995 to 2006 at Biogen Idec (IDEC from 1995 to 2004), where he had responsibility for analytical and formulation development, protein purification, and physicochemical/biochemical characterization supporting numerous IND and BLA submissions, including those for the commercial products RITUXAN® and ZEVALIN®. His last position with Biogen Idec was Director of Analytical and Protein Biochemistry within the Discovery Research group. Prior to IDEC, Dr. LaBarre spent two years at Vical, Inc. in the Analytical Methods Development group and he began his career at Hybritech in San Diego, where he held positions in Regulatory Affairs and Manufacturing Technical Support, focusing on conjugated/radiolabeled antibody technologies and analytical chemistry.


Dr. LaBarre received his B.S. in Chemistry from Southampton College of Long Island University and his Ph.D. in Bioinorganic Chemistry from the University of Arizona.

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