New study tracks fabry drug Elfabrio's Real-World impact
NCT ID NCT06663358
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows about 100 adults with Fabry disease who are taking or planning to take the medication Elfabrio. Researchers will monitor kidney function, heart health, and disease markers over time to see how well the drug works and if any side effects occur. The goal is to understand the drug's real-world safety and effectiveness.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Emory University School of Medicine
RECRUITINGAtlanta, Georgia, 30322, United States
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General Hospital Slovenj Gradec
RECRUITINGSlovenj Gradec, 2380, Slovenia
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Infusion Associates
RECRUITINGGrand Rapids, Michigan, 49525, United States
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Lysosomal & Rare Disorder Research & Treatment Center (LRDRTC)
RECRUITINGFairfax, Virginia, 22030, United States
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Northwestern University - Feinberg School of Medicine - Ann & Robert H. Lurie Children's Hospital of Chicago
RECRUITINGChicago, Illinois, 60611, United States
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Salford Royal
RECRUITINGSalford, Greater Manchester, M6 8HD, United Kingdom
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The Royal Free Hospital
RECRUITINGLondon, NW3 2QG, United Kingdom
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University Hospitals Birmingham NHS Foundation Trust, Queen Elizabeth Hospital
RECRUITINGEdgbaston, Birmingham, B152TH, United Kingdom
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University of Alabama at Birmingham
RECRUITINGBirmingham, Alabama, 35294, United States
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University of Iowa Hospitals and Clinics
RECRUITINGIowa City, Iowa, 52242, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can continued lucerastat access help fabry patients?
- Can a single gene infusion rewrite the story of fabry disease?
- Fabry disease sperm study halted early
- Heart study reveals hidden link between blood vessels and muscle blockage
- Taiwan study sheds light on rare fabry mutation and treatment effects