Impact of long-term elosulfase alfa on activities of daily living in patients with Morquio a syndrome in an open-label, multi-center, phase 3 extension study

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dc.contributor.author Hendriksz, Christian J.
dc.contributor.author Parini, Rossella
dc.contributor.author AlSayed, Moeenaldeen D.
dc.contributor.author Raiman, Julian
dc.contributor.author Giugliani, Roberto
dc.contributor.author Mitchell, John J.
dc.contributor.author Burton, Barbara K.
dc.contributor.author Guelbert, Norberto
dc.contributor.author Stewart, Fiona J.
dc.contributor.author Hughes, Derralynn A.
dc.contributor.author Matousek, Robert
dc.contributor.author Hawley, Sara M.
dc.contributor.author Decker, Celeste
dc.contributor.author Harmatz, Paul R.
dc.date.accessioned 2018-04-19T08:24:56Z
dc.date.available 2018-04-19T08:24:56Z
dc.date.issued 2018-02
dc.description Supplementary file 1. Items in the MPS Health Assessment Questionnaire (MPS-HAQ). en_ZA
dc.description Supplementary file 2. Items in the MPS Health Assessment Questionnaire (MPS-HAQ) (A) showing impairment in the self-care and mobility domains (score ≥ 1) and the caregiver-assistance domain (score > 1) in ≥ 70% of patients and (B) scored “unable to complete” or “complete assistance required” in ≥ 15% of patients in the MOR-005 ITT population. en_ZA
dc.description Supplementary file 3. Baseline demographics of patients from the MOR-005 intent-to-treat (ITT) and modified per-protocol (MPP) population and comparable patients from the MorCAP natural history study included in the 2-year analysis. en_ZA
dc.description.abstract BACKGROUND : Long-term safety and efficacy of elosulfase alfa enzyme replacement therapy (ERT) were assessed in 173 patients with Morquio A syndrome (mucopolysaccharidosis IVA) in a 96-week, open-label, multi-center, phase 3 extension study (MOR-005) of the pivotal 24-week, placebo-controlled study (MOR-004). Changes in efficacy endpoints were evaluated over 120 weeks, from MOR-004 baseline to MOR-005 week 96. We report the impact of ERT on activities of daily living (ADL) across three domains (mobility, self-care, and caregiver-assistance), as assessed by the Mucopolysaccharidosis Health Assessment Questionnaire (MPS-HAQ) after 72 and 120 weeks or approximately 1 and 2 years. RESULTS : Mean baseline MPS-HAQ domain scores showed impairments in mobility, self-care, and independence. The MOR-005 intent-to-treat population (ITT; N =169, including 158 with 2 years follow-up) showed sustained significant reductions (representing improvements) in mobility and self-care domain least square (LS) mean scores vs. baseline at 1 and 2 years and a non-significant decrease in the caregiver-assistance domain at 2 years. At week 120, LS mean (SE) changes from baseline were−0.5 (0.1) for mobility (P =0.002),−0.4 (0.1) for selfcare (P =0.001), and −1.0 (0.5) for caregiver-assistance (P= 0.06) (ITT population). Improvements in MPSHAQ domain scores vs. baseline at 1 and 2 years were greater in patients continuously treated with the weekly dosing regimen than in the total MOR-005 population and statistically significant across domains. A comparable untreated cohort of patients from the Morquio A Clinical Assessment Program (MorCAP) natural history study (ITT population, N =94, including 37 with 2 years follow-up) showed no improvement over 2 years, with two of the three domains worsening (LS mean (SE) changes from baseline: 0.3 (0.3) for mobility, 0.4 (0.2) for self-care, −0.5 (0.8) for caregiver-assistance). Changes in LS mean scores vs. baseline were statistically significantly different between MOR-005 and MorCAP for the mobility domain (−0.7 (SE 0.4), P=0.0490) and the self-care domain (−0.7 (SE 0.3), P=0.0146) at 2 years. en_ZA
dc.description.department Paediatrics and Child Health en_ZA
dc.description.librarian am2018 en_ZA
dc.description.sponsorship This study and support in the process of manuscript development were funded by BioMarin Pharmaceutical Inc. The site in Monza (Dr. Parini) received continuous economical support for the clinical work of the Center from Fondazione Pierfranco and Luisa Mariani. Dr. Mitchell receives research support from Dr. Eleanor Mackenzie Harpur Pediatric Endowment Fund. This publication was supported in part (Dr. Harmatz) by the National Center for Advancing Translational Sciences, National Institutes of Health (NIH), through UCSF-CTSI Grant Number UL1 TR000004. en_ZA
dc.description.uri http://www.elsevier.com/locate/ymgme en_ZA
dc.identifier.citation Hendriksz, C.J., Parini, R., AlSayed, M.D. et al. 2018, 'Impact of long-term elosulfase alfa on activities of daily living in patients with Morquio a syndrome in an open-label, multi-center, phase 3 extension study', Molecular Genetics and Metabolism, vol. 123, no. 2, pp. 127-134. en_ZA
dc.identifier.issn 1096-7192 (print)
dc.identifier.issn 1096-7206 (online)
dc.identifier.other 10.1016/j.ymgme.2017.11.015
dc.identifier.uri http://hdl.handle.net/2263/64650
dc.language.iso en en_ZA
dc.publisher Elsevier en_ZA
dc.rights © 2017 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/). en_ZA
dc.subject Morquio A syndrome en_ZA
dc.subject Elosulfase alfa en_ZA
dc.subject Disability en_ZA
dc.subject Activities of daily living (ADL) en_ZA
dc.subject Enzyme replacement therapy (ERT) en_ZA
dc.subject Disease en_ZA
dc.subject Endurance en_ZA
dc.subject Safety en_ZA
dc.subject Respiratory function en_ZA
dc.subject Mucopolysaccharidosis IVA en_ZA
dc.subject Mucopolysaccharidosis (MPS) en_ZA
dc.title Impact of long-term elosulfase alfa on activities of daily living in patients with Morquio a syndrome in an open-label, multi-center, phase 3 extension study en_ZA
dc.type Article en_ZA


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