drugset / Trial / NCT03153319

Study to Evaluate the Safety and Efficacy of Adalimumab in MPS I, II, and VI

NCT03153319

RandomizedParallel-groupQuadruple-blindTreatment

Summary

Randomized, double-blind, placebo-controlled, parallel-group, single-center study followed by open-label phase, to evaluate the effects of adalimumab compared to placebo on the change from baseline in joint and skeletal disease in children and adults with mucopolysaccharidosis (MPS) I, II or VI.

Timeline

Start
2017-06-05
Primary completion
2027-01
Completion
2027-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Adalimumab Monoclonal antibody 20 mg Subcutaneous
Subject Adalimumab Monoclonal antibody 40 mg Subcutaneous