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Clinical trial

Open-label, Non-controlled, Multicenter Long-term Study to Investigate the Safety and Efficacy of Xeomin® (Incobotulinumtoxin A, NT 201) for the Treatment of Spasticity of the Lower Limb(s) or of Combined Spasticity of Upper and Lower Limb in Children and Adolescents (Age 2 - 17 Years) With Cerebral Palsy

NCT01905683 is registered in ClinicalTrials.gov with Merz Pharmaceuticals GmbH as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Open-label, Non-controlled, Multicenter Long-term Study to Investigate the Safety and Efficacy of Xeomin® (Incobotulinumtoxin A, NT 201) for the Treatment of Spasticity of the Lower Limb(s) or of Combined Spasticity of Upper and Lower Limb in Children and Adolescents (Age 2 - 17 Years) With Cerebral Palsy
Lead sponsor
Merz Pharmaceuticals GmbH
Phase
Phase 3
Overall status
Completed
Start date
August 31, 2013
Completion date
January 31, 2017
Enrollment
370 (actual)
Sites
43

Conditions

As the registry lists them; a condition with its own page is linked.

lower limb and combined lower limb and upper limb spasticity due to cerebral palsy