To confirm the robustness of the CRC749 inhaler.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
111
Fluticasone Propionate / Salmeterol administered using CRC749 inhaler
Mylan Investigational Site
London, United Kingdom
Mylan Investigational Site
Manchester, United Kingdom
In vitro Measurement of Emitted Dose
CRC749 inhaler robustness will be assessed by in vitro testing of the CRC749 inhaler after 3 weeks of patient use of the MGR001 product.
Time frame: 3 Weeks
Adverse Events
Time frame: 3 Weeks
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