In one
clinical trial, the benefits of long-term ERT were maintained
in people who switched to
Zavesca. People with type 1 Gaucher disease who had been
taking ERT for an average of 5.6 years maintained the benefits
of ERT in liver and
spleen
size, hemoglobin concentration, and platelet count after
6 months on Zavesca.2,3
1. Cox T, Lachmann R, Hollak C, et
al. Novel oral treatment of Gaucher’s
disease with N-butyldeoxynojirimycin (OGT 918) to decrease
substrate
biosynthesis. Lancet. 2000;355:1481–1485.
2. Zavesca® (miglustat) package insert. Actelion, Ltd.
2003.
3. Data on file, Actelion Pharmaceuticals US, Inc.
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