A prospective multicenter observational post authorization safety sub-registry to characterize the long-term safety profile of commercial use of eliglustat (Cerdelga®) in adult patients with Gaucher disease (ELISAFE)

11/02/2016
16/02/2026
EU PAS number:
EUPAS11998
Study
Finalised
Documents
Study protocol
Initial protocol
English (626.47 KB - PDF) View document
Updated protocol
English (640.63 KB - PDF) View document
Study results
Study report
Abstract of study report
English (372.67 KB - PDF) View document
Other information