drugset / Trial / NCT01298180

Is There a Sensibility Increased in the Growth Hormone at Child With Prader-Willi Syndrome?

NCT01298180

Phase 4 Completed 111 enrolled University Hospital, Toulouse
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to estimate the sensibility at the growth hormone in vivo at the children presenting a Prader-Willi syndrome (SPW) in comparison with children presenting a deficit in growth hormone (GHD).

Timeline

Start
2009-01
Primary completion
2013-05
Completion
2013-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Somatropin Protein / enzyme biologic

Indications