drugset / Trial / NCT03081247
To Assess the Efficacy and Safety of PT010 Compared to PT009 in Subjects With Moderate to Very Severe Chronic Obstructive Pulmonary Disease
RandomizedParallel-groupDouble-blindTreatment
Summary
This is a 12-week chronic-dosing study to assess the efficacy and safety of BGF MDI compared to BFF MDI in subjects with moderate to very severe COPD.
Timeline
- Start
- 2018-04-16
- Primary completion
- 2018-12-07
- Completion
- 2018-12-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Glycopyrronium | Unknown | 14.4 ug | Inhaled |
| Background | Budesonide | Small molecule | 320 ug | Inhaled |
| Background | Formoterol | Other / unclassified | 9.6 ug | Inhaled |