Efficacy Study of SYN006 HFA MDI in Asthma Patients
Status:
Completed
Trial end date:
2014-08-01
Target enrollment:
Participant gender:
Summary
The objective of the study is to evaluate the dose response of SYN006 HFA MDI, which is a
combination drug product of budesonide and procaterol hydrochloride, in asthma patients.
Patients with mild to moderate asthma will be recruited. There will be two study medication
administered in this study. The investigational medication is SYN006 (Budesonide/Procaterol
hydrochloride, 180 mcg/10 mcg per inhalation) and the active comparative medication is
Ventolin (Salbutamol sulfate 100 mcg per inhalation). The study medication will be
administered by oral inhalation with the supervision of the investigator or a qualified
staff.