Phase III, randomized, double-blind, active-controlled, parallel-group study, comparing the efficacy, safety and tolerability of the fixed dose combination of FF/UMEC/VI with the fixed dose dual combination of FF/VI, administered once-daily via a dry powder inhaler in subjects with inadequately controlled ASTHMA.
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- STATUS
- Recruiting
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- sponsor
- GlaxoSmithKline
Summary
Phase III, randomized, double-blind, active-controlled, parallel-group study, comparing the efficacy, safety and tolerability of the fixed dose combination of FF/UMEC/VI with the fixed dose dual combination of FF/VI, administered once-daily via a dry powder inhaler in subjects with inadequately controlled ASTHMA.
Description
This study is comparing a triple fixed-dose combination product compared to a dual fixed-dose combination product in patients with asthma not adequately controlled. This study is for adults age 18 and above. There is compensation provided for time and travel. The study duration is a minimum of 24 weeks and a maximum of 52 weeks depending upon your time of enrollment. For more information, please contact our office at 636-946-1650
Details
| Condition | Asthma |
|---|---|
| Clinical Study Identifier | TX147792 |
| Sponsor | GlaxoSmithKline |
| Last Modified on | 23 November 2020 |
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