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VivaGel(R) Demonstrates Anti-HIV and Herpes Activity Following Human Administration
Date:8/4/2009

The retention of potent activity several hours after administration can only enhance the commercial prospects of VivaGel(R)," Dr Fairley added.

There were no serious adverse events during the study, and as previously announced the data indicate VivaGel(R) was well-tolerated.

The study was conducted in Melbourne at the Centre for Clinical Studies and in collaboration with the Burnet Institute. The study was funded by the U.S. National Institutes of Health (NIH), National Institute of Allergy and Infectious Diseases (NIAID), Division of AIDS (DAIDS), under Contract No. HHSN266200500042C.*

* The following statement is included in accordance with the requirements of Contract No. HHSN266200500042C:

The content of this announcement does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. Government.

    For further information:

    Media
    Buchan Consulting
    Rebecca Wilson
    Tel: +61 3 9866 4722
    Mob: +61 417 382 391
    rwilson@bcg.com.au

    Ellie Papathanasiou
    Tel: +61 2 9237 2800
    epapathanasiou@bcg.com.au

    Starpharma
    www.starpharma.com

    Dr Jackie Fairley
    Chief Executive Officer
    +61 3 8532 2704

    Ben Rogers
    Company Secretary
    +61 3 8532 2702
    ben.rogers@starpharma.com


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SOURCE Starpharma
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