Study identifier:PT001102
ClinicalTrials.gov identifier:NCT03358147
EudraCT identifier:N/A
CTIS identifier:N/A
A Randomized, Double-Blind, Parallel Group, Multi-Center 24-Week Study Comparing the Efficacy and Safety of Three Doses of PT001 to Placebo and Open-label Spiriva® Respimat® in Subjects With Persistent Asthma
asthma
Phase 2/3
No
GP MDI 28.8 μg, GP MDI 14.4 μg, GP MDI 7.2 μg, Placebo MDI, Spiriva Respimat 2.5 μg
All
1077
Interventional
12 Years - 80 Years
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Aug 2020 by Pearl Therapeutics, Inc.
Pearl Therapeutics, Inc.
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: GP MDI 28.8 μg GP MDI 14.4 μg per actuation taken as 2 inhalations BID | Drug: GP MDI 28.8 μg GP MDI (PT001)14.4 μg per actuation taken as 2 inhalations BID Other Name: GP |
Experimental: GP MDI 14.4 μg GP MDI 7.2 μg per actuation taken as 2 inhalations BID | Drug: GP MDI 14.4 μg GP MDI (PT001) 7.2 μg per actuation taken as 2 inhalations BID Other Name: GP |
Experimental: GP MDI 7.2 μg GP MDI 3.6 μg per actuation taken as 2 inhalations BID | Drug: GP MDI 7.2 μg GP MDI (PT001) 3.6 μg per actuation taken as 2 inhalations BID Other Name: GP |
Placebo Comparator: Placebo MDI Taken as 2 inhalations BID | Drug: Placebo MDI Placebo taken as 2 inhalations BID Other Name: Placebo |
Other: Spiriva Respimat 2.5 μg Open Label Spiriva Respimat 2.5 μg | Drug: Spiriva Respimat 2.5 μg Spiriva Respimat 2.5 μg QD (open-label) Other Name: Spiriva Respimat |