Fp MDPI
Sponsors
Teva Branded Pharmaceutical Products R&D, Inc.
Conditions
AsthmaPersistent Asthma
Phase 1
Phase 2
A Study of the Effectiveness and Safety of Different Doses of Fluticasone Propionate Taken From a Dry Powder Inhaler in Adolescents and Adults Who Have Asthma That is Not Controlled by Asthma Medications Not Containing Steroids
CompletedNCT01479621
Start: 2012-01-31End: 2013-07-31Updated: 2017-06-05
A Study of the Effectiveness and Safety of Different Doses of Fluticasone Propionate Taken From a Dry Powder Inhaler (Puffer) in Adolescents and Adults Who Have Asthma That is Not Controlled by High Dose Inhaled Corticosteroid Asthma Medications
CompletedNCT01576718
Start: 2012-04-30End: 2013-10-31Updated: 2018-05-08
Dose Ranging Study of the Salmeterol Component of Fluticasone /Salmeterol Spiromax Compared to Fluticasone Spiromax and Advair Diskus in Asthma Subjects
CompletedNCT01772368
Start: 2013-01-31End: 2013-06-30Updated: 2017-06-12
Phase 3
Study of Fluticasone Propionate MDPI Compared With Fluticasone/Salmeterol MDPI in Adolescent and Adult Patients With Persistent Asthma
CompletedNCT02139644
Start: 2014-06-30End: 2015-09-30Updated: 2021-11-12
Efficacy and Safety Study of FP MDPI Compared With FS MDPI in Adolescent and Adult Patients With Persistent Asthma
CompletedNCT02141854
Start: 2014-06-30End: 2015-09-30Updated: 2021-11-09
Long-Term Safety Study of Fluticasone Propionate (Fp) Multidose Dry Powder Inhaler (MDPI) and Fluticasone Propionate/Salmeterol (FS) MDPI in Patients With Persistent Asthma
CompletedNCT02175771
Start: 2014-07-31End: 2015-07-31Updated: 2021-11-09