05.05.2014 09:33:30

Press Release: MagForce AG and MagForce USA, Inc. Announce FDA Pre-IDE Meeting

MagForce AG / MagForce AG and MagForce USA, Inc. Announce FDA Pre-IDE Meeting . Processed and transmitted by Nasdaq OMX Corporate Solutions. The issuer is solely responsible for the content of this announcement.

Berlin, Germany and Nevada, USA, May 5, 2014 - MagForce AG (Frankfurt, Entry Standard, XETRA: MF6), a leading medical device company in the field of nanomedicine focused on oncology, together with its subsidiary MagForce USA, Inc. are pleased to report that an in-person meeting was held with the U.S. Food and Drug Administration's (FDA) Center for Devices and Radiological Health to discuss FDA's response to MagForce's NanoTherm(R) Therapy Pre-Submission of late December, 2013.

"We received very constructive feedback on our submission and have a better understanding of the issues and process for registration of NanoTherm(R) therapy in the USA. MagForce USA, Inc. will lead with the treatment of recurrent Glioblastoma in concert with MagForce AG's post marketing clinical trial in Germany, which has already begun enrolling patients. We are confident that MagForce AG's extensive pre-clinical and clinical studies will provide the background for a timely submission of an Investigational Device Exemption (IDE) for the application of NanoTherm(R) Therapy," commented Ben J. Lipps, CEO of MagForce AG and MagForce USA.

Assisting MagForce with its USA registration efforts are Drs. Larry Kessler, Professor and Chair of the Department of Health Services School of Public Health, University of Washington, and Donna-Bea Tillman, Ph.D., M.P.A., FRAPS, of Biologics Consulting Group, Alexandria, VA.

About MagForce AG

MagForce AG, listed in the entry standard (MF6), together with its subsidiary MagForce USA, Inc. is a leading medical device company in the field of nanomedicine in oncology. The Group's proprietary, NanoTherm(R) therapy, enables the targeted treatment of solid tumors through the intratumoral generation of heat via activation of superparamagnetic nanoparticles. NanoTherm(R), NanoPlan(R), and NanoActivator(TM) are components of the therapy and have received EU-wide regulatory approval as medical devices for the treatment of brain tumors. MagForce, NanoTherm(R), NanoPlan(R), and NanoActivator(TM) are trademarks of MagForce AG in selected countries. For more information, please visit www.magforce.com.

Disclaimer

This release may contain forward-looking statements and information which may be identified by formulations using terms such as "expects", "aims", "anticipates", "intends", "plans", "believes", "seeks", "estimates" or "will". Such forward-looking statements are based on our current expectations and certain assumptions, which may be subject to a variety of risks and uncertainties. The results actually achieved by MagForce AG may substantially differ from these forward-looking statements. MagForce AG assumes no obligation to update these forward-looking statements or to correct them in case of developments, which differ from those, anticipated.

Contact:

Anne Hennecke

MC Services AG

T +49 211 529252-22

F +49 211 529252-29

M +49 151 12 555 759

Email: anne.hennecke@mc-services.eu

MagForce_Press Release_May 05, 2014: http://hugin.info/143761/R/1782465/610112.pdf

This announcement is distributed by NASDAQ OMX Corporate Solutions on behalf of NASDAQ OMX Corporate Solutions clients.

The issuer of this announcement warrants that they are solely responsible for the content, accuracy and originality of the information contained therein.

Source: MagForce AG via Globenewswire

HUG#1782465

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MagForce AG

Max-Planck-Strasse 3 Berlin Germany

WKN: A0HGQF;ISIN: DE000A0HGQF5;

Listed: Freiverkehr in Börse Stuttgart,

Freiverkehr in Börse Berlin,

Freiverkehr in Börse Düsseldorf,

Entry Standard in Frankfurter Wertpapierbörse,

XETRA in Frankfurter Wertpapierbörse;

http://www.magforce.de/english/home1.html (END) Dow Jones Newswires

   May 05, 2014 03:01 ET (07:01 GMT)- - 03 01 AM EDT 05-05-14

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