drugset / Trial / NCT01697319
Efficacy and Safety Study of BMN 110 for Morquio A Syndrome Patients Who Have Limited Ambulation
NaSingle-groupOpen-labelTreatment
Summary
The primary objective of this study is to evaluate the effect of 2.0 mg/kg/week BMN 110 in a patient population that has limited ambulation, in a period of up to 144 weeks.
Timeline
- Start
- 2012-08
- Primary completion
- 2014-10
- Completion
- 2014-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | elosulfase alfa | Protein / enzyme biologic | 2 mg/kg | Intravenous |