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Pervasis Therapeutics Receives FDA Clearance for Pivotal Phase 3 Trial of Vascugel(R)
Date:2/1/2010

l after one year.(2) (3) Vascugel may represent a fundamentally new approach to preventing AV access failure by helping to regulate the body's healing response following the creation of an AV access site.

This news release contains certain forward-looking statements that involve risks and uncertainties. Such statements are only predictions and the company's actual results may differ materially from those anticipated in these forward-looking statements. Factors that may cause such differences include the timing of clinical trials, the risk that products that appeared promising in early research and clinical trials do not demonstrate safety or efficacy in clinical trials and the risk that the company will not obtain approval to market its products.

(1) http://kidney.niddk.nih.gov/kudiseases/pubs/kustats/index.htm. Last accessed January 27, 2010.

(2) Dixon et al. DAC Study Group. Effect of dipyridamole plus aspirin on hemodialysis graft patency. N Engl J Med. 2009; 360: 2191-2201.

(3) Hayashi et al. Vascular access for hemodialysis. Nat Clin Pract Nephrol. 2006; 2: 504-513.

    
    
    Company Contact:
    Margaret O'Toole
    Pervasis Therapeutics, Inc.
    617-871-1201
    
    Media Contact: 
    Jaren Irene Madden
    Feinstein Kean Healthcare
    617-761-6727

SOURCE Pervasis Therapeutics, Inc.

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SOURCE Pervasis Therapeutics, Inc.
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