Persistent growth-promoting effects of vosoritide in children with achondroplasia are accompanied by improvements in physical and social aspects of health-related quality of life
- PMID: 39305160
- DOI: 10.1016/j.gim.2024.101274
Persistent growth-promoting effects of vosoritide in children with achondroplasia are accompanied by improvements in physical and social aspects of health-related quality of life
Abstract
Purpose: Evaluate the impact of vosoritide on health-related quality of life in children with achondroplasia.
Methods: Participants received vosoritide (15 μg/kg/day) in an extension trial (NCT03424018) after having participated in a placebo-controlled trial (NCT03197766).
Results: The population comprised 119 participants (mean [SD] age 9.7 [2.6] years). Mean treatment duration was 4 (0.78) years. At year 3, the largest mean (SD) changes were observed in the Quality of Life of Short Stature Youth physical score (5.99 [19.41], caregiver reported; 6.32 [20.15], self-reported) and social score (2.85 [8.29] and 6.76 [22.64], respectively). Changes were greatest in participants with ≥1 SD increase in height z-score (physical: 11.36 [19.51], caregiver-reported [n = 38]; 8.48 [21.83], self-reported [n = 28]) (social: 5.84 [15.45] and 9.79 [22.80], respectively). To determine how domain scores may change with age in untreated persons, models were produced using observational/untreated-person data. A 1-year increase in age was associated with a change of 0.16 (SE, 0.55) and 0.16 (0.50), for caregiver-reported physical and social domain scores, respectively. Self-reported scores changed by 1.45 (0.71) and 1.92 (0.77), respectively.
Conclusion: These data suggest that after 3 years of treatment, vosoritide demonstrates a positive effect on physical and social functioning among children with achondroplasia, particularly in children with a more pronounced change in height z-score.
Keywords: Achondroplasia; QoLISSY; Quality of life; Vosoritide.
Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Conflict of Interest All authors were investigators in this clinical trial except for Richard Rowell, Andrea Low, Ian Sabir, Alice Huntsman-Labed, and Jonathan Day, who are employees of the funder (BioMarin). Antonio Leiva-Gea has received consulting fees from BioMarin, has participated as a clinical trial investigator for BioMarin and QED Therapeutics, has received speaker fees from BioMarin, MBA, and EAF, and has received travel support from BioMarin and MBA. Carlos A. Bacino has received consulting fees from BioMarin and has participated as clinical trial investigator for Roche, BioMarin and Ascendis. Carlos E. Prada has received consulting fees from BioMarin, Sanofi, and Takeda, has participated as a clinical trial investigator for BioMarin, Sanofi, Hemoshear, and Prevail, and has received speaker payments from Sanofi. Julie E. Hoover-Fong has received consulting fees from BioMarin, Ascendis, QED Therapeutics, Innoskel, and Tyra, has received research grants from Alexion, has participated as a clinical trial investigator for BioMarin, QED Therapeutics, and Pfizer/Therachon, has received speaker fees from Medscape, and has received travel support from BioMarin, QED Therapeutics, and Tyra. Klaus Mohnike has received consulting payments from BioMarin, QED Therapeutics and Novo Nordisk, has participated as a clinical trial investigator for BioMarin, and has received speaker fees and travel support from BioMarin and Novo Nordisk. Lynda E. Polgreen has received consulting fees from BioMarin, Lysogene, and Denali, has participated as a clinical trial investigator for BioMarin, Pfizer, and Takeda, and has received travel support from BioMarin. Melita Irving has received consulting fees from BioMarin, QED Therapeutics/Bridge Bio, Ascendis, Sanofi, and Tyra, has participated as a clinical trial investigator for BioMarin, QED Therapeutics/Bridge Bio, and Ascendis, has received speaker fees from BioMarin, QED Therapeutics/Bridge Bio, Ascendis, Ipsen, and Sandoz, and has received travel support from BioMarin, QED Therapeutics/Bridge Bio, and Ascendis. Paul Harmatz has received consultancy fees from Grace Science, Rallybio, Neurogene, Novel Pharma, and Orchard Therapeutics, has received speaker fees, travel support, and travel grants from BioMarin, has received research funding from Adrenas, Amicus, Ascendis, ASPA, Azafaros, BioMarin, Calcilytics, Denali, Homology, JCR Pharmaceuticals, Orphazyme, QED Therapeutics, RegenXbio, Sangamo, Takeda, Idorsia, Prevail,and Allievex, and has participated as a clinical trial investigator for BioMarin. Ravi Savarirayan has received consulting fees and travel support from BioMarin, QED Therapeutics, and Ascendis, and has participated as a clinical trial investigator for BioMarin, QED Therapeutics, Ascendis, and Sanofi. Takuo Kubota has received speaker payments from BioMarin and Novo Nordisk and research grants from Eli Lilly. William R. Wilcox has received consulting fees from BioMarin and has participated as a clinical trial investigator for BioMarin. All other authors declare no conflicts of interest.
Publication types
MeSH terms
Substances
Associated data
LinkOut - more resources
Full Text Sources
Medical
