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Clinical Trial Summary

The main aim of this study is to learn more about the safety profile of Elaprase in Indian children and adults with hunter syndrome. Participants will receive Elaprase once per week over a 3-hour period which can be reduced to 1 hour as determined by the study doctor. Participants will need to visit the clinic weekly during the duration of the study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05058391
Study type Interventional
Source Takeda
Contact Shire Contact
Phone +1 866 842 5335
Email ClinicalTransparency@takeda.com
Status Recruiting
Phase Phase 4
Start date April 21, 2022
Completion date September 30, 2024

See also
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