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