drugset / Trial / NCT00537602
Miglustat / OGT 918 in the Treatment of Cystic Fibrosis
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
Outcome
Outcome not reported
Stopped: “Methodology applied did not meet all criteria required per guidelines”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Miglustat | Small molecule | 200 mg | Oral |