drugset / Trial / NCT02204163

Study to Assess the Efficacy and Safety of Eutropin in Prader-Willi Syndrome

NCT02204163

Phase 3 Completed 34 enrolled LG Life Sciences
RandomizedParallel-groupOpen-labelTreatment

Summary

Evaluate the efficacy and safety after treatment of Eutropin® inj. compared to Genotropin® in infants/toddlers with Prader-Willi syndrome

Timeline

Start
2014-06
Primary completion
2017-12
Completion
2017-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Eutropin Protein / enzyme biologic 0.24 mg/kg
Comparator Somatropin Protein / enzyme biologic 0.24 mg/kg

Indications