{"id":13,"date":"2022-08-23T12:43:31","date_gmt":"2022-08-23T12:43:31","guid":{"rendered":"https:\/\/naglazymehcp-dev-001.azurewebsites.net\/en-us\/naglazyme\/?page_id=13"},"modified":"2024-08-27T20:39:25","modified_gmt":"2024-08-27T20:39:25","slug":"home","status":"publish","type":"page","link":"https:\/\/hcp.biomarin.com\/en-us\/naglazyme\/","title":{"rendered":"Home"},"content":{"rendered":"
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Look Forward with NAGLAZYME\u00ae<\/sup> (galsulfase)\n<\/h1>\n

See the long-term impact of NAGLAZYME in patients with MPS VI<\/strong><\/p>\n

Learn More<\/a><\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n <\/div>\n\n

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NAGLAZYME\u00ae<\/sup> (galsulfase) is the first and only enzyme replacement therapy (ERT) for people with Maroteaux-Lamy syndrome (MPS VI)1<\/sup> <\/h2>\n <\/div>\n <\/div>\n <\/div>\n<\/div>\n\n
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Sustained benefits with NAGLAZYME2<\/sup>\n<\/h4>\n \n

Learn more about the long-term impact of NAGLAZYME on MPS VI.<\/p>\n \n <\/div>\n

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Read More<\/a><\/p>\n <\/div>\n<\/div>\n\n

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Importance of compliance\n<\/h4>\n \n

ERT is a lifelong journey for your patients. Learn more about helping them stay compliant.<\/p>\n \n <\/div>\n

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Read More<\/a><\/p>\n <\/div>\n<\/div>\n\n

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Comprehensive team management\n<\/h4>\n \n

NAGLAZYME is a key part of MPS VI patient care, in addition to a multidisciplinary care team.2,3<\/sup><\/p>\n \n <\/div>\n

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Read More<\/a><\/p>\n <\/div>\n<\/div>\n\t\t\t<\/div>\n\t\t<\/div>\n\t<\/div>\n<\/div>\n\n

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References:\n<\/h4>\n\t\t\t\t\t\t
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  1. National MPS Society,\u00a0MPS VI (Maroteaux-Lamy syndrome);\u00a0https:\/\/mpssociety.org\/learn\/diseases\/mps-vi\/<\/a> (Accessed March 2023).\n<\/span><\/li>\n
  2. Giugliani R, Lampe C, Guffon N, et al<\/em>. Natural history and galsulfase treatment in mucopolysaccharidosis VI (MPS VI, Maroteaux\u2013Lamy syndrome)\u201410-year follow-up of patients who previously participated in an MPS VI Survey Study. Am J Med Genet A<\/em>. 2014;164A(8):1953-1964. doi:10.1002\/ajmg.a.36584.\n<\/span><\/li>\n
  3. Akyol MU, Alden TD, Amartino H, et al<\/em>. Recommendations for the management of MPS VI: systematic evidence- and consensus-based guidance. Orphanet J Rare Dis<\/em>. 2019;14:118.\n<\/span><\/li>\n <\/ol>\n\t\t\t\t\t<\/div>\n\t<\/div>\n<\/div>","protected":false},"excerpt":{"rendered":"","protected":false},"author":4,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"inline_featured_image":false,"footnotes":""},"class_list":["post-13","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"\nBioMarin Naglazyme HCP EN-US<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/hcp.biomarin.com\/en-us\/naglazyme\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"BioMarin Naglazyme HCP EN-US\" \/>\n<meta property=\"og:url\" content=\"https:\/\/hcp.biomarin.com\/en-us\/naglazyme\/\" \/>\n<meta property=\"og:site_name\" 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