drugset / Trial / NCT00537602

Miglustat / OGT 918 in the Treatment of Cystic Fibrosis

NCT00537602

Phase 2 Terminated 6 enrolled Actelion
RandomizedCrossoverQuadruple-blindTreatment

Summary

Cystic fibrosis is a genetic disease caused by mutation of the cystic fibrosis transmembrane conductance regulator (CFTR). The purpose of the study is to investigate the effects of miglustat on CFTR function in cystic fibrosis patients.

Timeline

Start
2007-11
Primary completion
2008-02
Completion
2008-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Miglustat Small molecule 200 mg Oral

Indications