Study to Evaluate the Effect of Adding five different compounds to Fluticasone Propionate 100 mcg Inhalation Powder Twice Daily in Uncontrolled Asthmatic Subjects โฅ12 Years of Age. - Trial 2010-019466-81
Access comprehensive clinical trial information for 2010-019466-81 through Pure Global AI's free database. This phase not specified trial is sponsored by GlaxoSmithKline Research & Development and is currently status unknown. The study focuses on Asthma.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to EU Clinical Trials Register data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
Sponsor & Location
GlaxoSmithKline Research & Development
GlaxoSmithKline Research & Development Ltd.
Timeline & Enrollment
N/A
N/A
N/A
Primary Outcome
The primary efficacy endpoint was trough (AM pre-dose and pre-rescue bronchodilator) forced expiratory volume in 1 second (FEV1) at the end of the 6-week treatment period.
ICD-10 Classifications
Data Source
EU Clinical Trials Register
2010-019466-81
Non-Device Trial

