Relative Bioavailability Study With Abediterol Administered Via Three Different Inhalation Devices in Healthy Volunteers.

PHASE1TerminatedINTERVENTIONAL
Enrollment

25

Participants

Timeline

Start Date

January 28, 2020

Primary Completion Date

April 3, 2020

Study Completion Date

April 3, 2020

Conditions
Chronic Obstructive Pulmonary Disease
Interventions
DRUG

Abediterol (2.4 μg)

2.4 μg (delivered dose) abediterol via PARI LC SPRINT nebuliser

DRUG

Abediterol (4.8 μg)

4.8 μg (delivered dose) abediterol via PARI LC SPRINT nebuliser

DRUG

Abediterol (2.4 μg)

2.4 μg (delivered dose) abediterol via OMRON NE-C900-E nebuliser

DRUG

Abediterol (2.5 μg)

2.5 μg (nominal dose) abediterol via DPI, reference

Trial Locations (1)

14050

Research Site, Berlin

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

AstraZeneca

INDUSTRY