<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Berweck S</submitter><funding>Merz (Germany)</funding><pagination>585</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9505819</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(9)</volume><pubmed_abstract>IncobotulinumtoxinA, a pure botulinumtoxinA formulation, is free of accessory proteins. This analysis provides pooled safety data from phase 3 trials of children/adolescents (2-17 years), investigating incobotulinumtoxinA for the treatment of spasticity associated with cerebral palsy (at doses ≤20 U/kg (max. 500 U) per injection cycle (IC) for ≤6 ICs; three trials) or sialorrhea associated with neurologic disorders (at total doses of 20-75 U per IC for ≤4 ICs; one trial) for ≤96 weeks. Safety endpoints included the incidences of different types of treatment-emergent adverse events (TEAEs) and immunogenicity. IncobotulinumtoxinA dose groups were combined. Of 1159 patients (mean age 7.3 years, 60.4% males) treated with incobotulinumtoxinA, 3.9% experienced treatment-related TEAEs, with the m</pubmed_abstract><journal>Toxins</journal><pubmed_title>Safety Profile and Lack of Immunogenicity of IncobotulinumtoxinA in Pediatric Spasticity and Sialorrhea: A Pooled Analysis.</pubmed_title><pmcid>PMC9505819</pmcid><funding_grant_id>N/A</funding_grant_id><pubmed_authors>Banach M</pubmed_authors><pubmed_authors>Geister TL</pubmed_authors><pubmed_authors>Heinen F</pubmed_authors><pubmed_authors>Vacchelli M</pubmed_authors><pubmed_authors>Dabrowski E</pubmed_authors><pubmed_authors>Berweck S</pubmed_authors><pubmed_authors>Schroeder AS</pubmed_authors><pubmed_authors>Hanschmann A</pubmed_authors><pubmed_authors>Althaus M</pubmed_authors><pubmed_authors>Bonfert MV</pubmed_authors><pubmed_authors>Chambers HG</pubmed_authors><pubmed_authors>Gaebler-Spira D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety Profile and Lack of Immunogenicity of IncobotulinumtoxinA in Pediatric Spasticity and Sialorrhea: A Pooled Analysis.</name><description>IncobotulinumtoxinA, a pure botulinumtoxinA formulation, is free of accessory proteins. This analysis provides pooled safety data from phase 3 trials of children/adolescents (2-17 years), investigating incobotulinumtoxinA for the treatment of spasticity associated with cerebral palsy (at doses ≤20 U/kg (max. 500 U) per injection cycle (IC) for ≤6 ICs; three trials) or sialorrhea associated with neurologic disorders (at total doses of 20-75 U per IC for ≤4 ICs; one trial) for ≤96 weeks. Safety endpoints included the incidences of different types of treatment-emergent adverse events (TEAEs) and immunogenicity. IncobotulinumtoxinA dose groups were combined. Of 1159 patients (mean age 7.3 years, 60.4% males) treated with incobotulinumtoxinA, 3.9% experienced treatment-related TEAEs, with the m</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-21T20:12:43.079Z</modification><creation>2025-04-05T17:54:36.626Z</creation></dates><accession>S-EPMC9505819</accession><cross_references><pubmed>36136523</pubmed><doi>10.3390/toxins14090585</doi></cross_references></HashMap>