A Multi-Country Observational Study of Safety and Effectiveness of Elfabrio® in Fabry Patients

Part of paid clinical trials in Birmingham, Alabama.

Sponsor
Chiesi Farmaceutici S.p.A.
Study ID
NCT06663358
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Pegunigalsidase-alfa — DRUG
    Administered via intravenous (IV) infusion under conditions of routine clinical care

Study Details

A multi-centre, multi-country, observational, non-interventional, retrospective and prospective (hybrid) study among Fabry disease participants treated with pegunigalsidase alfa (Elfabrio®) in routine clinical care.

Key Dates

Start date
Nov 6, 2024
Status verified
Nov 2024
Primary completion
Nov 30, 2029
Completion
Nov 30, 2029

Study Design

Enrollment
100 participants (estimated)

Arms

  • Arm: Cardiac Cohort
    Patients with Fabry-related cardiac disease
  • Arm: Naïve Cohort
    Patients naïve to prior Fabry disease treatment
  • Arm: Long-Term Cohort
    Patients previously participating in the pegunigalsidase alfa open label extension study and transitioning to routine care

Primary Outcome Measure

Estimated Glomerular Filtration Rate (eGFR) [ Time Frame: 4 years ]

Central Contacts

Locations (6)

FacilityCityStateZIPSite coordinators
University of Alabama at BirminghamBirminghamAlabama35294
Eric Wallace, MD
+1 205-975-2935
Emory University School of MedicineAtlantaGeorgia30322
William Wilcox, MD
404-778-8518
Northwestern University - Feinberg School of Medicine - Ann & Robert H. Lurie Children's Hospital of ChicagoChicagoIllinois60611
Carlos Prada, MD
+1 312-227-3724
University of Iowa Hospitals and ClinicsIowa CityIowa52242
John Bernat
319-356-2007
Infusion AssociatesGrand RapidsMichigan49525
Michael Mawby, MD
Lysosomal & Rare Disorder Research & Treatment Center (LRDRTC)FairfaxVirginia22030
Ozlem Goker-Alpan

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