Fabry Disease Clinical Trial
Official title:
Cardiovasculorenal Phenotyping in Fabry Disease Through Noninvasive Testing
A longitudinal pilot study will be conducted to determine if there are additional testing modalities that are effective in broadly phenotyping subclinical dysfunction in patients with Fabry disease. Individual patients will undergo serial testing over a two-year period to evaluate for changes in their cardiovasculaorenal function during this period. Novel modalities evaluated will include measures of arterial stiffness, ambulatory blood pressure monitoring, cardiopulmonary exercise testing (CPET), and novel serum and urine biomarkers. The benefit of these measures being evaluated is that they are noninvasive, can be performed rapidly, and have reduced costs compared to the current standard screening modalities. Results from these evaluations will be compared to cMRI and standard urine and serum biomarkers performed clinically per local standard of care. The results will also be compared to both published normative data and data from patients with diabetes mellitus, who have a similar microvascular disease process to patients with Fabry disease.
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Status | Clinical Trial | Phase | |
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Recruiting |
NCT04893889 -
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N/A | |
Completed |
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A Long Term Follow-Up Study of Fabry Disease Subjects Treated With FLT190
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Phase 1/Phase 2 | |
Completed |
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Study to Compare the Efficacy and Safety of Oral AT1001 and Enzyme Replacement Therapy in Patients With Fabry Disease
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Phase 3 | |
Completed |
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A 12-Week Safety and Pharmacodynamic Study of AT1001 (Migalastat Hydrochloride) in Female Participants With Fabry Disease
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Phase 2 | |
Withdrawn |
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Complement Activation in the Lysosomal Storage Disorders
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Completed |
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Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of Migalastat in Pediatric Subjects (Aged 12 to <18 Years)
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Phase 3 | |
Withdrawn |
NCT04143958 -
To Assess the Glycosphingolipid Clearance and Clinical Effects of Switching to Agalsidase Beta (Fabrazyme) Versus Continuing on Agalsidase Alfa (Replagal) in Male Patients With Classic Fabry Disease
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Phase 4 | |
Recruiting |
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Podocyturia - Predictor of Renal Dysfunction in Fabry Nephropathy
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N/A | |
Completed |
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Sleepiness and Sleep-disordered Breathing in Fabry Disease. A Prospective Cohort Study.
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N/A | |
Recruiting |
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Non-invasive Assessment of Intraocular Pressure in MPS by Use of the Ocular Response Analyzer.
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N/A | |
Completed |
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A Phase I, Randomized, Single-Blind, Four-Period Cross-Over, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety and Pharmacokinetics of Single Oral Doses of GR181413A/AT1001 in Healthy Japanese Subjects
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Phase 1 | |
Completed |
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A Study of Two Fabrazyme (Agalsidase Beta) Dosing Regimens in Treatment-naïve, Male Pediatric Patients Without Severe Symptoms
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Phase 3 | |
Completed |
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Dosing Study of Replagal in Patients With Fabry Disease
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Phase 2 | |
Completed |
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Ophthalmic Findings During 10-year Enzyme Substitution of Danish Fabry Patients.
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Phase 4 | |
Recruiting |
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Autoimmune and Inflammatory Response Biomarkers in Fabry Disease
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Recruiting |
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Active, not recruiting |
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N/A | |
Terminated |
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Open-label Long-term Safety Study of AT1001 (Migalastat Hydrochloride) in Participants With Fabry Disease Who Have Completed a Previous AT1001 Study
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Phase 2 | |
Active, not recruiting |
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Open Label Extension Study of 1 mg/kg Pegunigalsidase Alfa Every 2 Weeks in Patients With Fabry Disease
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Phase 3 | |
Recruiting |
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Assess Urine Biomarkers to Predict Nephropathy in Fabry Disease
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