This is a 54-week Phase 4, open label, single arm study to evaluate the safety and the efficacy of Fabrazyme (agalsidase beta) as enzyme replacement therapy (ERT) in Chinese participants with Fabry Disease.
Study participation for each patient will be total of 54 weeks which will include 4 weeks of screening, 48 weeks of treatment period and 2 weeks of post study treatment observation
Condition | Fabry's Disease |
---|---|
Treatment | agalsidase beta |
Clinical Study Identifier | NCT05054387 |
Sponsor | Genzyme, a Sanofi Company |
Last Modified on | 13 May 2022 |
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