<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17</volume><submitter>Guilbert TW</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Dupilumab, a fully human monoclonal antibody, blocks the shared receptor component for interleukins-4/-13, key and central drivers of type 2 inflammation in multiple diseases. This post hoc analysis of the Phase 3 LIBERTY ASTHMA VOYAGE study (NCT02948959) evaluated the efficacy of dupilumab in children aged 6 to 11 years with moderate-to-severe asthma with a type 2 inflammatory phenotype (blood eosinophil count ≥150 cells/µL or fractional exhaled nitric oxide [FeNO] ≥20 ppb) and a history of 1, 2, or ≥3 prior exacerbations. The impact of baseline type 2 biomarker levels on the efficacy of dupilumab in this population was also investigated.&lt;h4>Patients and methods&lt;/h4>Patients were stratified by the number of exacerbations in the prior year (1, 2, or ≥3) and level of FeNO or blood eosinophil count at baseline. Endpoints included rate of severe exacerbations, percentage of non-exacerbators, and change from baseline in both lung function parameters (pre- and post-bronchodilator [BD] percent predicted forced expiratory volume in 1 s (ppFEV&lt;sub>1&lt;/sub>) and ppFEV&lt;sub>1&lt;/sub>/forced vital capacity [FVC] ratio) and Asthma Control Questionnaire 7 Interviewer-Administered (ACQ-7-IA) score.&lt;h4>Results&lt;/h4>A total of 350 patients were included in this analysis. Across patients with 1, 2, or ≥3 prior exacerbations and different levels of type 2 biomarkers, dupilumab reduced the risk of severe asthma exacerbations vs placebo by 53.0-96.0% and improved both pre-BD ppFEV&lt;sub>1&lt;/sub> and pre-BD FEV&lt;sub>1&lt;/sub>/FVC ratio at Week 52. Dupilumab led to significant reductions in ACQ-7-IA scores in all groups of patients by Week 52.&lt;h4>Conclusion&lt;/h4>In children with uncontrolled, moderate-to-severe asthma with a type 2 phenotype, dupilumab consistently reduced the risk of asthma exacerbations, improved lung function, and reduced ACQ-7-IA scores, regardless of exacerbation history.</pubmed_abstract><journal>Journal of asthma and allergy</journal><pagination>143-159</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10928922</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Impact of Exacerbation History on Dupilumab Efficacy in Children with Uncontrolled Moderate-to-Severe Asthma: LIBERTY ASTHMA VOYAGE Study.</pubmed_title><pmcid>PMC10928922</pmcid><pubmed_authors>Begin P</pubmed_authors><pubmed_authors>Guilbert TW</pubmed_authors><pubmed_authors>Rowe PJ</pubmed_authors><pubmed_authors>Radwan A</pubmed_authors><pubmed_authors>Fiocchi AG</pubmed_authors><pubmed_authors>Ledanois O</pubmed_authors><pubmed_authors>Tolcachier A</pubmed_authors><pubmed_authors>de Mir I</pubmed_authors><pubmed_authors>Deniz Y</pubmed_authors><pubmed_authors>Jacob-Nara JA</pubmed_authors><pubmed_authors>Altincatal A</pubmed_authors><pubmed_authors>Phipatanakul W</pubmed_authors><pubmed_authors>Gall R</pubmed_authors><pubmed_authors>Katelaris CH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of Exacerbation History on Dupilumab Efficacy in Children with Uncontrolled Moderate-to-Severe Asthma: LIBERTY ASTHMA VOYAGE Study.</name><description>&lt;h4>Purpose&lt;/h4>Dupilumab, a fully human monoclonal antibody, blocks the shared receptor component for interleukins-4/-13, key and central drivers of type 2 inflammation in multiple diseases. This post hoc analysis of the Phase 3 LIBERTY ASTHMA VOYAGE study (NCT02948959) evaluated the efficacy of dupilumab in children aged 6 to 11 years with moderate-to-severe asthma with a type 2 inflammatory phenotype (blood eosinophil count ≥150 cells/µL or fractional exhaled nitric oxide [FeNO] ≥20 ppb) and a history of 1, 2, or ≥3 prior exacerbations. The impact of baseline type 2 biomarker levels on the efficacy of dupilumab in this population was also investigated.&lt;h4>Patients and methods&lt;/h4>Patients were stratified by the number of exacerbations in the prior year (1, 2, or ≥3) and level of FeNO or blood eosinophil count at baseline. Endpoints included rate of severe exacerbations, percentage of non-exacerbators, and change from baseline in both lung function parameters (pre- and post-bronchodilator [BD] percent predicted forced expiratory volume in 1 s (ppFEV&lt;sub>1&lt;/sub>) and ppFEV&lt;sub>1&lt;/sub>/forced vital capacity [FVC] ratio) and Asthma Control Questionnaire 7 Interviewer-Administered (ACQ-7-IA) score.&lt;h4>Results&lt;/h4>A total of 350 patients were included in this analysis. Across patients with 1, 2, or ≥3 prior exacerbations and different levels of type 2 biomarkers, dupilumab reduced the risk of severe asthma exacerbations vs placebo by 53.0-96.0% and improved both pre-BD ppFEV&lt;sub>1&lt;/sub> and pre-BD FEV&lt;sub>1&lt;/sub>/FVC ratio at Week 52. Dupilumab led to significant reductions in ACQ-7-IA scores in all groups of patients by Week 52.&lt;h4>Conclusion&lt;/h4>In children with uncontrolled, moderate-to-severe asthma with a type 2 phenotype, dupilumab consistently reduced the risk of asthma exacerbations, improved lung function, and reduced ACQ-7-IA scores, regardless of exacerbation history.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2025-04-19T05:51:55.202Z</modification><creation>2025-04-19T05:51:55.202Z</creation></dates><accession>S-EPMC10928922</accession><cross_references><pubmed>38476213</pubmed><doi>10.2147/JAA.S416292</doi></cross_references></HashMap>