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Innovacell - Biotechnologie

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Press releases

2011-10-10

Innovacell presents at Bio-Europe Congress in Düsseldorf

Innovacell Biotechnologie AG today announced to be one of the presenters at the upcoming Bio-Europe Congress in Düsseldorf, Germany from October 31st - November 2nd.



The three-day congress will feature a hybrid of business, regulatory and scientific topics. The speakers will be drawn from pharmaceutical and biotech companies, such as regulators and cell and gene therapy developers.

 

Ekkehart Steinhuber, Innovacell’s CEO, will be presenting Innovacell’s clinical trial results of the Phase IIb trial for ICES13, a product for treating stress urinary incontinence. The study was carried out in 32 centers in four European countries. A Phase III trial is already approved by authorities and will start in the fourth quarter of 2011. The session will focus on the technology of the ultrasound guided injection device and the results of the Phase IIb trial.

 

ICES13 addresses a fast growing market. There are about seven million patients in the world’s seven biggest pharmaceutical markets, which would profit from a treatment with ICES13 – therefore are the USA and Japan besides Europe as well interesting areas.

 

About Innovacell Biotechnologie AG


Innovacell Biotechnologie AG is a privately held biotechnology company based in Innsbruck, Austria. The Company is engaged in the clinical development and commercialization of autologous (patients’ own), minimally invasive, potentially curative (“once-in-a-life-time”) cell therapies to re-establish functionality of sphincter muscle in patients with stress urinary incontinence (SUI) or fecal incontinence (FI). The Company is lead by an experienced management team, owns and operates one of Europe’s largest, state-of-the-art GMP facilities.

 

ICES13 for SUI patients is currently in late-stage clinical development (Phase III) and ICEF15 for persons with FI is in mid-stage testing (Phase IIa). Each product comprises an autologous myoblast cell suspension that is implanted by means of two different, specifically designed, proprietary and CE-marked injectors.


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