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New Data On Xeomin® (IncobotulinumtoxinA) To Be Presented At The 15th International Congress Of Parkinson's Disease And Movement Disorders (MDS)
Date:6/8/2011

01) in each group (using paired t-test).

About XEOMIN®

In nature, Clostridium botulinum produces the toxin in association with accessory (complexing) proteins. Manufacturers isolate the therapeutically active botulinum neurotoxin together with the accessory (complexing) proteins. XEOMIN (incobotulinumtoxinA) is manufactured using a proprietary process that isolates in an additional purification step the therapeutic component and eliminates accessory proteins.

More than 127,000 patients have been treated with XEOMIN worldwide since 2005. XEOMIN is approved in 21 countries worldwide for the treatment of cervical dystonia and blepharospasm and in 17 countries for the treatment post stroke upper limb spasticity. It is currently not approved in the U.S. for the treatment of spasticity.

XEOMIN is the only botulinum toxin product that does not require refrigeration prior to reconstitution.

Merz Pharmaceuticals GmbH (www.merz.com):

Merz Pharmaceuticals, a member of the MerzPharma Group of companies, is an innovative and international specialty healthcare company specializing in the research, development and marketing of pharmaceuticals for the treatment of neurological and psychiatric diseases. In addition to developing XEOMIN®, the company has developed memantine (Axura®) -- the first drug for the treatment of moderate to severe Alzheimer's disease. The company also focuses on the development of innovative therapies within the therapeutic areas of hepatology, metabolic disease and dermatology.

XEOMIN is a registered trademark of MerzPharma GmbH & Co KGaA.


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1. FDA Approves Merz Pharmaceuticals Xeomin® (incobotulinumtoxinA) for the Treatment of Cervical Dystonia and Blepharospasm
2. Xeomin® (incobotulinumtoxinA) - a Botulinum Toxin Free From Accessory Proteins - Now Available in the U.S.
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