Ongoing
Research Projects |
- SAS30021- Principal Investigator-
A Stratified, Randomized, Double Blind, Placebo-Controlled,
Parallel-Group, 12-Week Trial Evaluating the Safety and
Efficacy of the Fluticasone Propionate/Salmeterol Diskus
Combination Product 100/50mcg Once Daily Versus Fluticasone
Propionate Diskus 100 mcg Once Daily and Placebo in Symptomatic
Pediatric Subjects (4-11 Years) With Asthma.
- SAM40027- Principal Investigator-
Gaining Optimal Asthma Control (GOAL). A Step-Up Comparison
Of The Level Of Asthma Control Achieved With Salmeterol/
Fluticasone Propionate Combination Compared With Fluticasone
Propionate Alone.
- SD-00400732- Sub-Investigator
- A Safety And Efficacy Study Of Two Dosage Levels Of Pulmicort
Respules (Budenoside Inhalation Suspension, 0.5 Or 1 Mg/Day)
Versus Placebo In Infants Between Ages Of Six & Twelve
Months With Mild To Moderate Asthma.
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