drugset / Trial / NCT01349803
PT003 MDI Cardiovascular Safety Study
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This study is primarily a safety study. The primary and secondary endpoints are based on 24-hour Holter monitor assessments obtained on Day 14 relative to baseline.
Timeline
- Start
- 2011-05
- Primary completion
- 2011-11
- Completion
- 2011-11
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Formoterol | Other / unclassified | 9.6 ug | Inhaled |
| Subject | Formoterol | Other / unclassified | 12 ug | Inhaled |
| Subject | Glycopyrrolate | Small molecule | 36 ug | Inhaled |