PSD psivida limited

psivida enters licensing negotiations with major g

  1. 48 Posts.
    pSivida Enters Licensing Negotiations with Major Global Pharma
    for Drug Delivery Technologies

    pSivida to receive US$990k for three months exclusive negotiation

    rights and additional preclinical study

    BOSTON & PERTH, Australia--(BUSINESS WIRE)--December 26, 2006 Global drug delivery company pSivida Limited (ASX:PSD) (NASDAQ:PSDV) (Xetra:PSI) announced today that it is has entered into an exclusive negotiation period with a major global pharmaceutical company, to acquire a worldwide, royalty bearing license to make, use and sell products using pSivida's drug delivery technologies.

    -- The pharmaceutical company will make payments totaling US$990k

    (AU$1.3m) to pSivida for the right to exclusively negotiate a

    licensing agreement with the Company for a period of three

    months and to fund the cost of a preclinical study.

    -- The preclinical study will focus on an evaluation of pSivida's

    drug delivery technologies in a very significant product

    opportunity.

    -- This announcement follows several 12 month evaluation

    agreements of pSivida's drug delivery technologies with large

    companies including this major global pharmaceutical company.

    -- pSivida recently completed a placement to raise US$2.9m

    (AU$3.7m) before costs to Australian and European investors.

    -- This raising is an interim financing measure prior to the

    expected closing of the definitive documents with Nordic

    Biotech Advisors for a US$4.0m (AU$5.1m) corporate investment

    in pSivida and a US$22.0m (AU$28.2m) investment over time in a

    "Special Purpose Vehicle" (SPV) that is expected to fully fund

    pSivida's portion of costs to develop Medidur(TM) for the

    treatment of the chronic eye disease diabetic macular edema

    (DME).

    Dr. Roger Brimblecombe, CEO and Chairman of pSivida Limited said, "We are delighted to be working with this major global pharma and to build our relationship on the positive findings from their initial pre-clinical evaluation of our drug delivery technologies
 
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