drugset / Trial / NCT05058391

A Study of Elaprase in Children and Adults With Hunter Syndrome (Mucopolysaccharidosis II) in India

NCT05058391

Phase 4 Completed 5 enrolled Takeda
NaSingle-groupOpen-labelTreatment

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.

Timeline

Start
2022-04-21
Primary completion
2024-04-06
Completion
2024-04-18

Drugs

EvaluationDrugModalityDoseRoute
Subject idursulfase Protein / enzyme biologic 0.5 mg/kg Intravenous

Indications

No indication recorded.