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

dc.contributor.authorHendriksz, Christian J.
dc.contributor.authorParini, Rossella
dc.contributor.authorAlSayed, Moeenaldeen D.
dc.contributor.authorRaiman, Julian
dc.contributor.authorGiugliani, Roberto
dc.contributor.authorMitchell, John J.
dc.contributor.authorBurton, Barbara K.
dc.contributor.authorGuelbert, Norberto
dc.contributor.authorStewart, Fiona J.
dc.contributor.authorHughes, Derralynn A.
dc.contributor.authorMatousek, Robert
dc.contributor.authorHawley, Sara M.
dc.contributor.authorDecker, Celeste
dc.contributor.authorHarmatz, Paul R.
dc.date.accessioned2018-04-19T08:24:56Z
dc.date.available2018-04-19T08:24:56Z
dc.date.issued2018-02
dc.descriptionSupplementary file 1. Items in the MPS Health Assessment Questionnaire (MPS-HAQ).en_ZA
dc.descriptionSupplementary 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.descriptionSupplementary 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.abstractBACKGROUND : 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.departmentPaediatrics and Child Healthen_ZA
dc.description.librarianam2018en_ZA
dc.description.sponsorshipThis 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.urihttp://www.elsevier.com/locate/ymgmeen_ZA
dc.identifier.citationHendriksz, 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.issn1096-7192 (print)
dc.identifier.issn1096-7206 (online)
dc.identifier.other10.1016/j.ymgme.2017.11.015
dc.identifier.urihttp://hdl.handle.net/2263/64650
dc.language.isoenen_ZA
dc.publisherElsevieren_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.subjectMorquio A syndromeen_ZA
dc.subjectElosulfase alfaen_ZA
dc.subjectDisabilityen_ZA
dc.subjectActivities of daily living (ADL)en_ZA
dc.subjectEnzyme replacement therapy (ERT)en_ZA
dc.subjectDiseaseen_ZA
dc.subjectEnduranceen_ZA
dc.subjectSafetyen_ZA
dc.subjectRespiratory functionen_ZA
dc.subjectMucopolysaccharidosis IVAen_ZA
dc.subjectMucopolysaccharidosis (MPS)en_ZA
dc.titleImpact 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 studyen_ZA
dc.typeArticleen_ZA

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