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Clinical Trial Summary

This is a multi-center trial to further extend the assessment of the safety and efficacy of taliglucerase alfa in adult subjects (≥18 years old) with Gaucher disease who have enrolled in Protocol PB-06-003. Subjects will continue to receive an intravenous (IV) infusion of taliglucerase alfa every two weeks. The duration of treatment will be a maximum of 21 months or until taliglucerase alfa is commercially available to the subject at the discretion of the Sponsor.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01422187
Study type Interventional
Source Pfizer
Contact
Status Completed
Phase Phase 3
Start date August 2011
Completion date September 2014

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