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Mucopolysaccharidosis type II

Hunter Syndrome
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Clinical Trials

This information is provided by ClinicalTrials.gov

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Displaying 1-10 of 19 results.
RGX-121 Gene Therapy in Patients With MPS II (Hunter Syndrome)
Status: Recruiting
Last Changed: Jan 09, 2020
First Received: Jun 21, 2018
Disease(s): Mucopolysaccharidosis Type II (MPS II)
Intervention(s): RGX-121
Locations: University of California San Francisco, Benioff Children's Hospital, Oakland, California, United States
Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
Children's Hospital of Pittsburgh - UPMC: Program for Neurodevelopment in Rare Disorders, Pittsburgh, Pennsylvania, United States
Hospital de Clinicas de Porto Alegre, Porto Alegre, RS, Brazil
A Study of Potential Treatment-Responsive Biomarkers in Hunter Syndrome
Status: Recruiting
Last Changed: Feb 18, 2020
First Received: Jul 05, 2019
Disease(s): Hunter Syndrome
Intervention(s): No Intervention
Locations: UCSF Benioff Children's Hospital, Oakland, California, United States
UPMC | Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, United States
Manchester Centre for Genomic Medicine, Manchester, United Kingdom
A Study of DNL310 in Pediatric Subjects With Hunter Syndrome
Status: Not yet recruiting
Last Changed: Jan 31, 2020
First Received: Jan 31, 2020
Disease(s): Mucopolysaccharidosis II
Intervention(s): DNL310
Study of Idursulfase-beta (GC1111) in Hunter Syndrome
Status: Not yet recruiting
Last Changed: Jan 26, 2016
First Received: Jan 26, 2016
Disease(s): Mucopolysaccharidosis II
Intervention(s): idursulfase beta, idursulfase
Hunter Outcome Survey (HOS)
Status: Recruiting
Last Changed: Mar 19, 2019
First Received: Sep 26, 2017
Disease(s): Hunter Syndrome
Locations: Shire, Lexington, Massachusetts, United States
A Study of GC1111 in Hunter Syndrom Patients
Status: Recruiting
Last Changed: Apr 24, 2019
First Received: Apr 19, 2019
Disease(s): Hunter Syndrome
Intervention(s): GC1111, Comparator
Locations: Samsug Medical Center, Seoul, Korea, Republic of
Intensive Pharmacovigilance Program for Elaprase (SHP ELA-701)
Status: Recruiting
Last Changed: May 09, 2019
First Received: Jul 11, 2018
Disease(s): Hunter Syndrome
Locations: Hospital Pediátrico de Sinaloa, Culiacán Rosales, México, Mexico
Hospital del Niño Tabasqueño, Villahermosa, Tabasco, Mexico
Hospital Centenario Miguel Hidalgo, Aguascalientes, Mexico
Hospital Infantil Federico Gomez, Ciudad de México, Mexico
... and 2 other locations.
Biomarker for Hunter Disease (BioHunter)
Status: Recruiting
Last Changed: Jul 10, 2019
First Received: Apr 06, 2011
Disease(s): Inguinal Hernia, Tonic-clonic, Glaucoma
Locations: Children Hospital, Faculty of Medicine, Cairo University, Cairo, Egypt
Ain Shams University, El Cairo, Egypt
Amrita Institute of Medical Sciences, Kerola, India
Navi Mumbai Institute of Research In Mental And Neurological Handicap (NIRMAN), Mumbai, India
Centenario Hospital Miguel Hidalgo, Aguascalientes, Mexico
... and 5 other locations.
Study to Evaluate the Safety and Efficacy of Adalimumab in MPS I and II
Status: Recruiting
Last Changed: Jul 02, 2019
First Received: May 15, 2017
Disease(s): Mucopolysaccharidosis I, Mucopolysaccharidosis II
Intervention(s): Adalimumab Injection [Humira], Saline Solution for Injection
Locations: Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California, United States
UCB Transplant of Inherited Metabolic Diseases With Administration of Intrathecal UCB Derived Oligodendrocyte-Like Cells
Status: Recruiting
Last Changed: Dec 03, 2019
First Received: Oct 02, 2014
Disease(s): Adrenoleukodystrophy, Batten Disease, Mucopolysaccharidosis II, Leukodystrophy, Globoid Cell, Leukodystrophy, Metachromatic, Neimann Pick Disease, Pelizaeus-Merzbacher Disease, Sandhoff Disease, Tay-Sachs Disease, Brain Diseases, Metabolic, Inborn, Alpha-Mannosidosis, Sanfilippo Mucopolysaccharidoses
Intervention(s): DUOC-01
Locations: Duke University Medical Center, Durham, North Carolina, United States