Clinical trial

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

NCT00074971 · Genzyme, a Sanofi Company, Industry · Completed

Key facts

NCT number NCT00074971
Title A Study of the Safety and Efficacy of Fabrazyme in Patients With Fabry Disease
Official title A Multi-center, Open-Label Extension Study of the Safety and Efficacy of Recombinant Human a-Galactosidase A (r-haGAL) Replacement in Patients With Fabry Disease
Lead sponsor Genzyme, a Sanofi Company, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Fabry Disease
Intervention type Drug
Interventions Fabrazyme (agalsidase beta)
Enrollment 58
Start date Oct 1, 1999
Completion Dec 1, 2004
First posted Dec 25, 2003
Last update posted Dec 4, 2013
Countries France, Netherlands, Puerto Rico, United Kingdom, United States

At a glance

  • 10–99 Study sites
  • No 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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