drugset / Trial / NCT02230566

A Phase 3 Study of UX003 Recombinant Human Betaglucuronidase (rhGUS) Enzyme Replacement Therapy in Patients With Mucopolysaccharidosis Type 7 (MPS 7)

NCT02230566 ↗

Phase 3 Completed 12 enrolled Ultragenyx Pharmaceutical Inc
RandomizedCrossoverQuadruple-blindTreatment

Summary

The Phase 3 study will use a novel randomized, intra-subject placebo-controlled, single crossover design, referred to as Blind Start, to evaluate the safety and efficacy of UX003. The Blind Start is a novel design whereby participants will be randomized to 1 of 4 groups, each representing a different treatment sequence, and will cross over to UX003 at different pre-defined time points in a blinded manner. All groups will receive a minimum of 24 weeks treatment with 4 mg/kg UX003 every other week (QOW).

Timeline

Start
2014-12
Primary completion
2016-05
Completion
2016-05

Outcome

Met primary endpoint

registry analysis (superiority test); UX003 4 mg/kg; p < 0.0001; LS Mean -64.82 (95% CI -69.66 to -59.98); GEE NCT02230566 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject vestronidase alfa Protein / enzyme biologic 4 mg/kg Intravenous