Safety and efficacy of repeat long-term incobotulinumtoxinA treatment for lower limb or combined upper/lower limb spasticity in children with cerebral palsy
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu klinické zkoušky, fáze III, časopisecké články, práce podpořená grantem
PubMed
34957963
PubMed Central
PMC9028655
DOI
10.3233/prm-210041
PII: PRM210041
Knihovny.cz E-zdroje
- Klíčová slova
- Botulinum toxins, Type A, cerebral palsy, movement disorders, muscle spasticity, paediatric,
- MeSH
- botulotoxiny typ A * škodlivé účinky MeSH
- dítě MeSH
- dolní končetina MeSH
- lidé MeSH
- mladiství MeSH
- mozková obrna * komplikace farmakoterapie MeSH
- nervosvalové látky * MeSH
- svalová spasticita farmakoterapie etiologie MeSH
- výsledek terapie MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze III MeSH
- práce podpořená grantem MeSH
- Názvy látek
- botulotoxiny typ A * MeSH
- incobotulinumtoxinA MeSH Prohlížeč
- nervosvalové látky * MeSH
PURPOSE: The open-label phase 3 "Treatment with IncobotulinumtoxinA in Movement Open-Label" (TIMO) study investigated longer-term safety and efficacy of incobotulinumtoxin A in children/adolescents with cerebral palsy (CP). METHODS: Patients on standard treatment, with unilateral or bilateral lower limb (LL) or combined upper limb (UL)/LL spasticity received four incobotulinumtoxinA injection cycles (16 or 20 Units/kg bodyweight total [maximum 400 or 500 Units] per cycle depending on ambulatory status/clinical pattern treated), each followed by 12-16 weeks' observation. Treatment for pes equinus was mandatory; flexed knee or adducted thigh were options for unilateral treatment and/or ULs for unilateral/bilateral treatment. The primary endpoint was safety; changes in Ashworth Scale and Gross Motor Function Measure-66 scores, and Global Impression of Change Scale scores at week 4 of each injection cycle were also evaluated. RESULTS: IncobotulinumtoxinA (≤500 Units for ≤98 weeks) was safe, well-tolerated, and effective across all endpoints for multipattern treatment of LL and combined LL/UL spasticity in ambulant/nonambulant children/adolescents with CP. Treatment effects increased with each injection cycle. No new/unexpected safety concerns were identified. CONCLUSION: IncobotulinumtoxinA showed a good safety and tolerability profile, with efficacy over multiple clinical presentations. As an adjunct treatment, it offers an effective, individualized treatment option for pediatric CP-related spasticity.
Beaumont Pediatric Physical Medicine and Rehabilitation Royal Oak Royal Oak MI USA
Department of Neurology Collegium Medicum Jagiellonian University Krakow Poland
Formerly of Merz North America Raleigh NC USA
Merz Pharmaceuticals Gmb H Frankfurt am Main Germany
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