BOTOX® Open-Label Treatment in Pediatric Upper Limb Spasticity

Study Identifier
191622-105
CT.gov Identifier
EudraCT Identifier
EUCTIS ID
Not available
For general inquiries, please contact
Study Complete

Results Available

Protocol
Available Language(s): English
Statistical Analysis Plan
Available Language(s): English

Study Details

Medical Condition
  • Pediatrics
  • Movement Disorders - Other
  • Stroke
  • Study Drug
  • Botulinum Toxin Type A
  • Phase
    Phase 3
    Sex
    Female & Male
    Age
    2 - 17 Years

    Protocol Summary

    This study will evaluate the long-term safety of BOTOX® (botulinum toxin Type A) for the treatment of pediatric upper limb spasticity.

    Study Locations

    Location
    Status
    Location
    ABS Health, LLC
    Pasadena, California, United States, 91106
    Status
    Not applicable
    Location
    Harrison Clinical Management
    Pomona, California, United States, 91767
    Status
    Not applicable
    Location
    Rady Children's Hospital San Diego
    San Diego, California, United States, 92123
    Status
    Not applicable
    Location
    Children's Hospital Colorado Dept. of PM&R
    Aurora, Colorado, United States, 80045
    Status
    Not applicable
    Location
    Associated Neurologists of Southern Connecticut, P.C.
    Fairfield, Connecticut, United States, 06824
    Status
    Not applicable
    Location
    New England Center for Clinical Research
    Stamford, Connecticut, United States, 06905
    Status
    Not applicable
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