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Clinical Trial Summary

This open-label Phase 2 study will evaluate the safety and efficacy of weekly 2.0 mg/kg/wk infusions of BMN 110 in pediatric patients, less than 5 years of age at the time of administration of the first dose of study drug, diagnosed with MPS IVA (Morquio A Syndrome) for up to 208 weeks.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01515956
Study type Interventional
Source BioMarin Pharmaceutical
Contact
Status Completed
Phase Phase 2
Start date October 2011
Completion date June 2016

See also
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Completed NCT02294877 - A Multicenter, Multinational, Observational Morquio A Registry Study (MARS)
Completed NCT01961518 - Screening an Orthopedic Population for Mildly-affected Individuals With Morquio Syndrome A and Maroteaux-Lamy Syndrome N/A
Recruiting NCT05284006 - Non-invasive Functional Assessment and Pathogenesis of Morquio A
Completed NCT01415427 - Long-Term Efficacy and Safety Extension Study of BMN 110 in Patients With Mucopolysaccharidosis IVA (Morquio A Syndrome) Phase 3
Recruiting NCT04532047 - In Utero Enzyme Replacement Therapy for Lysosomal Storage Diseases Phase 1
Completed NCT01920828 - Gait Analysis in MPS IVA
Terminated NCT01697319 - Efficacy and Safety Study of BMN 110 for Morquio A Syndrome Patients Who Have Limited Ambulation Phase 2
Terminated NCT01609062 - Safety and Exercise Study of Two Doses of BMN 110 for Morquio A Syndrome Phase 2
Approved for marketing NCT01858103 - BMN 110 US Expanded Access Program N/A