405
Participants
Start Date
September 28, 2017
Primary Completion Date
April 17, 2018
Study Completion Date
April 17, 2018
Albuterol sulfate (ABS)
ABS will be administered via eMDPI as per the dose and schedule specified in the arm.
Teva Investigational Site 14683, Pittsburgh
Teva Investigational Site 14713, Richmond
Teva Investigational Site 14692, Winston-Salem
Teva Investigational Site 14722, Greensboro
Teva Investigational Site 14696, Gastonia
Teva Investigational Site 14710, Charlotte
Teva Investigational Site 14715, Spartanburg
Teva Investigational Site 14718, Spartanburg
Teva Investigational Site 14719, Gaffney
Teva Investigational Site 14707, Union
Teva Investigational Site 14681, Charleston
Teva Investigational Site 14695, Mt. Pleasant
Teva Investigational Site 14691, Greenville
Teva Investigational Site 14686, Easley
Teva Investigational Site 14711, Daytona Beach
Teva Investigational Site 14694, Edgewater
Teva Investigational Site 14699, DeLand
Teva Investigational Site 14688, Orlando
Teva Investigational Site 14701, Miami
Teva Investigational Site 14689, Miami
Teva Investigational Site 14678, Miami
Teva Investigational Site 14725, Brandon
Teva Investigational Site 14704, Anniston
Teva Investigational Site 14682, Andalusia
Teva Investigational Site 14712, Mobile
Teva Investigational Site 14680, Grove City
Teva Investigational Site 14708, Columbus
Teva Investigational Site 14709, Toledo
Teva Investigational Site 14724, Willoughby
Teva Investigational Site 14703, Dayton
Teva Investigational Site 14679, Valparaiso
Teva Investigational Site 14705, Chesterfield
Teva Investigational Site 14717, Omaha
Teva Investigational Site 14716, San Antonio
Teva Investigational Site 14702, Peoria
Teva Investigational Site 14706, Gold River
Teva Investigational Site 14687, Spokane
Teva Investigational Site 14720, Waterbury
Teva Investigational Site 14677, North Dartmouth
Teva Investigational Site 14684, Toms River
Teva Branded Pharmaceutical Products R&D, Inc.
INDUSTRY