Viewing Study NCT00432666



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Study NCT ID: NCT00432666
Status: COMPLETED
Last Update Posted: 2010-12-15
First Post: 2007-02-07

Brief Title: IncobotulinumtoxinA Xeomin Versus Placebo in the Treatment of Post-stroke Spasticity of the Upper Limb
Sponsor: Merz Pharmaceuticals GmbH
Organization: Merz Pharmaceuticals GmbH

Study Overview

Official Title: Prospective Double-blind Placebo-controlled Randomized Multi-center Trial With an Open-label Extension Period to Investigate the Efficacy and Safety of incobotulinumtoxinA Xeomin in the Treatment of Post-stroke Spasticity of the Upper Limb
Status: COMPLETED
Status Verified Date: 2010-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: IncobotulinumtoxinA Xeomin is a botulinum toxin type A preparation free from complexing proteins ie free from proteins other than the active toxin Injected into the muscle incobotulinumtoxinA Xeomin causes local weakening Botulinum toxin type A is widely used for treatment of various neurological conditions This study will investigate the efficacy and safety of incobotulinumtoxinA Xeomin in the treatment of post-stroke spasticity of the upper limb
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None