Asthma Clinical Trial
Official title:
A Randomized, Double- or Evaluator-blind, Active- and Placebo-controlled, Single Dose, Seven-arm, Crossover Dose-ranging Study of A006 in Adult Asthma Patients
The main objective of this study is to evaluate the efficacy, dose-ranging and initial
safety profiles of A006, an Albuterol dry powder inhaler (DPI), in the dose range of 25 to
180 mcg per dosing in comparison to a DPI Placebo Control and an Albuterol metered dose
inhaler (MDI) Active Control.
This study will be conducted in male and female adult patients who have mild-to-moderate
persistent asthma for at least 6 months, but are otherwise generally healthy.
The main objective of this study is to evaluate the efficacy, dose-ranging and initial
safety profiles of A006, an Albuterol dry powder inhaler (DPI), in the dose range of 25 to
180 mcg per dose in comparison to the DPI Placebo Control and the Active (Reference)
Control. The study results of this study together with that of A006-B study will be utilized
to determine the optimum final dose range of A006 for further clinical studies.
The study will be conducted in male and female adult patients who have mild-to-moderate
persistent asthma but are otherwise generally healthy.
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