New Real-World study tracks fabry Drug's Long-Term impact on heart and kidneys
NCT ID NCT07109375
First seen Jun 27, 2026 · Last updated Jul 09, 2026 · Updated 2 times
Summary
This study follows 75 adults with Fabry disease who are taking or starting pegunigalsidase alfa to see how well it works and how safe it is over time in real-world settings. Researchers will check heart structure and function, kidney health, and exercise capacity. The goal is to understand if this enzyme replacement therapy helps control the disease long-term.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for FABRY DISEASE are added.
By submitting, you agree to our Terms of use
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
-
A.O. Sant'Anna e San Sebastiano
NOT_YET_RECRUITINGCaserta, Italy
-
A.O.U. Policlinico "Giaccone"
NOT_YET_RECRUITINGPalermo, Italy
-
AOU Federico II, Dipartimento di Nefrologia
NOT_YET_RECRUITINGNaples, Italy
-
AUSL Toscana Sud-Est - Ospedale San Donato
NOT_YET_RECRUITINGArezzo, Italy
-
Azienda Ospedaliera Universitaria Consorziale Policlinico Di Bari
RECRUITINGBari, Italy
-
Irccs Azienda Ospedaliero-Universitaria Di Bologna - Policlinico Di Sant'Orsola
RECRUITINGBologna, Italy
-
U.O.C. Nefrologia ASST Monza - Ospedale San Gerardo
NOT_YET_RECRUITINGMonza, Italy
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can early enzyme therapy save kidneys in fabry disease?
- 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