This study aims to study the efficacy (as measured by change in FEV1) and safety of two-week administration of oral QAV680 in the treatment of patients with asthma.'
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
37
Novartis Investigative Site
Berlin, Germany
Novartis Investigative Site
Munich, Germany
Novartis Investigative Site
Wiesbaden, Germany
Novartis Investigative Site
Ahmedabad, India
Measure: Change in Forced Expiratory Volume in one second (FEV1) as measured by Spirometry.
Time frame: 2 weeks
Measure: Change in Asthma Control Questionnaire (ACQ) score
Time frame: 2 weeks
Measure: Frequency of salbutamol usage
Time frame: 2 weeks
Measure: Change in exhaled Nitric Oxide (NO)
Time frame: 2 weeks
Home Monitoring Of FEV1 By PIKO Monitors
Time frame: Day 2 to Day 13
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Novartis Investigative Site
Mumbai, India
Novartis Investigative Site
Mysore, India
Novartis Investigative SIte
Nagpur, India