Intercell AG

euro adhoc: Intercell AG
other
Positive results for IntercellÂ’s Japanese Encephalitis Vaccine in pivotal Phase III Safety trial

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24.08.2006

» Results for Intercell’s Japanese Encephalitis virus vaccine in the
pivotal      Phase III safety trial, which included 2,683 randomized
subjects, are      positive » IntercellÂ’s JE vaccine was well
tolerated, no critical adverse events were      observed » With these
results, the preparations for the filing process with the United
States Food and Drug Administration (FDA) are fully on track for an
anticipated market launch in the United States in 2007

Intercell AG (VSE, "ICLL") announced today that the safety analyses for the pivotal Phase III safety trial of its investigational Japanese Encephalitis vaccine are positive.

The pivotal Phase III safety trial was conducted at 39 study sites in Austria, Germany, Romania, Israel, Australia, New Zealand and in the US, and included 2,683 randomized subjects. The study was designed to analyze the safety and tolerability of IntercellÂ’s investigational vaccine in a multicenter, multinational, double-blind, placebo-controlled randomized study.

Major endpoints of this study were the frequency of adverse events in both test groups, as well as local tolerability findings in both groups. First analyses of this trial show that IntercellÂ’s investigational Japanese Encephalitis vaccine was systemically and locally well tolerated. Overall, the local tolerability and general safety profile of the Intercell JE vaccine appeared to be comparable with placebo.

The Phase III clinical trial program consists of several additional clinical trials including a pivotal immunogenicity trial, a single shot trial, and a co-vaccination trial for travelers, which are all expected to be completed by early 2007. To date, more than 4,800 of the approximately 5,370 trial participants have been enrolled and vaccinated in these clinical trials. The pivotal Phase III clinical trial program is designed to meet regulatory requirements in the United States, Europe and Australia. Assuming approval by the regulatory authorities, the first market launch is anticipated for 2007. Preparations for the submission of a BLA (Biologics License Application) to the FDA have commenced.

Full clinical results of the pivotal immunogenicity trial are planned to be presented at the Annual Meeting of the American Society of Tropical Medicine and Hygiene (ASTMH), November 12-16, Atlanta, and full clinical results of the pivotal safety trial are planned to be presented at the 10th Conference of the International Society of Travel Medicine, May 20-24, 2007 in Vancouver, Canada.

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ots Originaltext: Intercell AG
Im Internet recherchierbar: http://www.presseportal.de

Further inquiry note:
Intercell AG
Mag. Katharina Wieser
Head of Corporate Communications
Tel. +43 1 20620-303
kwieser@intercell.com

Branche: Biotechnology
ISIN:      AT0000612601
WKN:        A0D8HW
Börsen:  Wiener Börse AG / official market



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