Clinical trial

A Study of the Safety and Efficacy of Fabrazyme in Patients With Fabry Disease

NCT00196716 · Genzyme, a Sanofi Company, Industry · Completed

Key facts

NCT number NCT00196716
Title A Study of the Safety and Efficacy of Fabrazyme in Patients With Fabry Disease
Official title A Multicenter, Open-label Study of Low Dose Maintenance Treatment of Fabrazyme (Recombinant Human Alpha-Galactosidase A (R-h Alpha-GAL)) Replacement Therapy in Patients With Fabry Disease
Lead sponsor Genzyme, a Sanofi Company, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Fabry Disease
Intervention type Biological
Interventions Fabrazyme (agalsidase beta)
Enrollment 21
Start date Jun 1, 2003
Primary completion Apr 1, 2006
Completion Mar 1, 2007
First posted Sep 20, 2005
Last update posted Apr 3, 2015
Countries Czechia, Estonia, Poland, Slovakia

At a glance

  • 1–9 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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