Abstract | OBJECTIVE: METHODS: This was a prospective, double-blind, randomized, placebo-controlled, multicenter clinical trial in botulinum toxin-treated or toxin-naïve CD patients. The primary outcome measure was change from baseline to Week 4 on the Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS) Total score. Adverse events (AEs) also were evaluated. RESULTS: Participants (N=233) were mostly women (66%), a mean of 52.8 years old, who had CD for a mean of 51.9 months. Of those, 39% were toxin-naïve. IncobotulinumtoxinA significantly improved TWSTRS-Total scores from baseline to Week 4 compared to placebo (placebo=-2.2; 120 U=-9.9, and 240 U=-10.9; 240 U vs. placebo p<0.001 and 120 U vs. placebo p<0.001). This effect persisted through to the end of the study. The most frequently reported AEs in the incobotulinumtoxinA groups were dysphagia, neck pain, and muscular weakness which were generally mild. INTERPRETATION:
IncobotulinumtoxinA (at doses of 120 U or 240 U) is a safe and effective treatment for CD in previously-treated as well as toxin-naïve subjects.
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Authors | Cynthia L Comella, Joseph Jankovic, Daniel D Truong, Angelika Hanschmann, Susanne Grafe, U.S. XEOMIN Cervical Dystonia Study Group |
Journal | Journal of the neurological sciences
(J Neurol Sci)
Vol. 308
Issue 1-2
Pg. 103-9
(Sep 15 2011)
ISSN: 1878-5883 [Electronic] Netherlands |
PMID | 21764407
(Publication Type: Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2011 Elsevier B.V. All rights reserved. |
Chemical References |
- Botulinum Toxins, Type A
- incobotulinumtoxinA
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Topics |
- Adult
- Aged
- Botulinum Toxins, Type A
(adverse effects, therapeutic use)
- Deglutition Disorders
(chemically induced)
- Double-Blind Method
- Female
- Humans
- Male
- Middle Aged
- Muscle Weakness
(chemically induced)
- Prospective Studies
- Torticollis
(drug therapy, physiopathology)
- Treatment Outcome
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