drugset / Trial / NCT00421122
Efficacy and Safety Study of Symbicort Turbuhaler in Chinese Patients With COPD
RandomizedParallel-groupTriple-blindTreatment
Summary
This study aims at evaluating efficacy and safety of Symbicort® Turbuhaler® in Chinese COPD patients as defined by GOLD treatment guidelines in order to obtain an approval for indication of COPD from Chinese State Food and Drug Administration.
Timeline
- Start
- 2006-09
- Primary completion
- —
- Completion
- 2007-11
Outcome
Met primary endpoint
paper this was significantly better (p < 0.001) than the small increase (0.03 L) observed in the BUD group after 24 weeks' treatment. PMID 22046961 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Budesonide | Small molecule | 200 ug | Inhaled |
| Subject | budesonide/formoterol | Unknown | — | Inhaled |
| Background | Terbutaline | Unknown | — | Inhaled |