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Mucopolysaccharidosis Type I clinical trials

View clinical trials related to Mucopolysaccharidosis Type I.

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NCT ID: NCT05634512 Recruiting - Clinical trials for Hematopoietic Cell Transplantation

Evaluation of Intravenous Laronidase Pharmacokinetics Before and After Hematopoietic Cell Transplantation in Patients With Mucopolysaccharidosis Type IH.

Start date: November 17, 2022
Phase:
Study type: Observational

This is a prospective, observational multicenter study to collect blood from patients with mucopolysaccharidosis type IH undergoing laronidase therapy and a stem cell transplant. Sixteen patients will be enrolled over a 24 month period.

NCT ID: NCT03576729 Completed - Clinical trials for Mucopolysaccharidosis Type I

MRS to Determine Neuroinflammation and Oxidative Stress in MPS I

Start date: November 1, 2018
Phase:
Study type: Observational

Neuroinflammation and oxidative stress have been shown to be present in persons with mucopolysaccharidosis type I (MPS I), but their effect on disease severity and disease progression is unknown. The investigator intends to employ brain magnetic resonance spectroscopy (MRS), a non-invasive technique, along with analysis of neuroinflammation and oxidative stress biomarkers in the blood, to measure and determine the level of oxidative stress and neuroinflammation, and their impact on clinical variability in MPS I patients.

NCT ID: NCT03161171 Completed - Coping Behavior Clinical Trials

Parental Coping With Challenging Behavior in Mucopolysaccharidosis Type I-III

Start date: July 6, 2017
Phase: N/A
Study type: Observational

The study quantitates behavioral challenges in mucopolysaccharidosis type I-III and parental coping strategies

NCT ID: NCT02437253 Recruiting - Clinical trials for Mucopolysaccharidosis Type II

Effects of Adalimumab in Mucopolysaccharidosis Types I, II and VI

Start date: May 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of the study is to collect preliminary data on whether the drug adalimumab (also called Humira) can decrease pain and stiffness, improve quality of life, and is safe in people with mucopolysaccharidosis type I, II, or VI. In this study people will be randomly assigned to one of two groups. One group will be treated with adalimumab the first 16 weeks of the study and then with a saline injection for the last 16 weeks of the study. The other group will start with the saline injection for 16 weeks and then switch to adalimumab for the last 16 weeks. The study subject and the study doctor and study coordinator will not know what group a subject is in until the study is done. Adalimumab is given as an injection, just under the skin, every 2 weeks. Both groups will have blood drawn at a screening visit, and then 7 more times over the 32 week study. There will be safety labs done (liver and immune function tests). Other safety tests include a chest X-ray and screening for tuberculosis exposure - these will be done at the screening visit and later in the study if there is concern for tuberculosis exposure or a persistent cough. The following will also be done at screening, the first, middle, and last study visits: 1) a pregnancy test in all girls 8 and older, 2) questionnaires that ask about pain, how MPS impacts social and physical function, and other quality of life questions, 3) height and weight. Finally, a physical exam, that includes for children and adolescents a check of where they are in puberty, will be done by a study physician at the first, middle, and last visits. There are risks to taking adalimumab that include redness and pain where the injection is given, a decreased ability to fight off infections, and others. The safety tests are designed to identify and decrease the risk associated with adalimumab. The study physicians believe that the potential benefit of adalimumab on pain, quality of life, and other MPS related problems outweigh the potential risks of treatment.

NCT ID: NCT02298712 Withdrawn - Clinical trials for Metabolism, Inborn Errors

Biomarker for Hurler Disease (BioHurler)

BioHurler
Start date: August 20, 2018
Phase:
Study type: Observational

Development of a new MS-based biomarker for the early and sensitive diagnosis of Hurler disease from plasma. Testing for clinical robustness, specificity and long-term stability of the biomarker.

NCT ID: NCT01870375 Completed - Clinical trials for Mucopolysaccharidosis Type II

Longitudinal Studies of Brain Structure and Function in MPS Disorders

Start date: September 2009
Phase:
Study type: Observational

Neurobehavioral function and quality of life are compromised in many patients with mucopolysaccharidosis (MPS) disorders. The long-term goals of this research are to: 1) more accurately inform patients/parents regarding potential neurobehavioral outcomes; 2) develop sensitive measures of disease progression and central nervous system (CNS) treatment outcome; and 3) help clinical researchers develop direct treatments for specific brain structures/functions. The investigators hypothesize that specific and localized neuroimaging and neuropsychological findings and their relationship will be distinct for each MPS disorder. It is further hypothesized that without treatment, functions will decline and structure will change over time in a predictable fashion, and will be related to locus of abnormality and stage of disease.