Dynavax Receives $600,000 SBIR Grant for TLR Research 
  BERKELEY, CA, Sep 07, 2011 (MARKETWIRE via COMTEX) -- Dynavax Technologies  Corporation (DVAX) today announced the receipt of a two-year Small Business  Innovation Research grant (SBIR) for $600,000. The Award is provided by the  National Institute of Allergy and Infectious Diseases and will be used to fund  research to characterize the role of the phosphoinositide 3-kinase (PI3K) in  preclinical models of skin autoimmune inflammation. 
  Scientists at Dynavax have shown that PI3K is required for the production of type  I interferon (IFN) by plasmacytoid dendritic cells (PDC) in response to TLR7 or  TLR9 stimulation (Journal of Experimental Medicine 2008). In subsequent studies,  the chronic activation of PDC and the IFN that they produced was shown to play a  role in skin autoimmune inflammation (Journal of Experimental Medicine 2010),  which makes PI3k an attractive target for skin diseases such as psoriasis,  cutaneous lupus, and dermatomyositis. 
  "This new grant supports preclinical studies focused on this key component of the  TLR signaling pathway as a target for the treatment of inflammatory skin  disorders. This work could well be complementary to our GSK development  partnership focused on TLR inhibitors," commented Robert L. Coffman, Ph.D., Vice  President and Chief Scientific Officer of Dynavax. 
  About Dynavax 
  Dynavax Technologies Corporation, a clinical-stage biopharmaceutical company,  discovers and develops novel products to prevent and treat infectious and  inflammatory diseases. The Company's lead product candidate is HEPLISAV(TM), a  Phase 3 investigational adult hepatitis B vaccine designed to provide rapid and  superior protection with fewer doses than current licensed vaccines. For more  information visit dynavax.com. 
  Forward Looking Statements 
  This press release contains "forward-looking statements," including statements  related to biological mechanisms and potential usefulness of the Company's  inhibitors. Actual results may differ materially from those set forth in this  press release due to the risks and uncertainties inherent in our business,  including whether results of completed studies can be replicated in human  studies, difficulties or delays in discovery or development, initiation and  completion of preclinical or clinical studies, the results of those studies and  the impact of those results on the initiation and completion of subsequent  studies and issues arising in the regulatory process; achieving our GSK agreement  objectives; our ability to obtain additional financing to support our operations;  and other risks detailed in the "Risk Factors" section of our current periodic  reports filed with the SEC. We undertake no obligation to revise or update  information herein to reflect events or circumstances in the future, even if new  information becomes available. Information on Dynavax's website at  dynavax.com is not incorporated by reference in the Company's current  periodic reports with the SEC. 
  Contact:  Michael Ostrach  Vice President and Chief Business Officer  510-665-7257  Email Contact |