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CompletedNCT02162485

Pharmacokinetic Study Comparing Salmeterol/Fluticasone Easyhaler Products and Seretide Diskus

Pharmacokinetic Study Comparing Salmeterol/Fluticasone Easyhaler Products and Seretide Diskus 50/500 µG/Inhalation; A Randomised, Open, Single Centre, Single Dose, Crossover Study in Healthy Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
129 (actual)
Sponsor
Orion Corporation, Orion Pharma · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

The purposes of this study is to compare the test products Salmeterol/fluticasone Easyhaler with marketed product Seretide Diskus in terms of the drug absorbed into the blood stream

Conditions

Interventions

TypeNameDescription
DRUGSalmeterol/fluticasone Easyhaler
DRUGSalmeterol/fluticasone Easyhaler with charcoal
DRUGSeretide Diskus
DRUGSeretide Diskus with charcoal

Timeline

Start date
2014-06-01
Primary completion
2015-09-01
Completion
2015-09-01
First posted
2014-06-12
Last updated
2015-09-29

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT02162485. Inclusion in this directory is not an endorsement.

Pharmacokinetic Study Comparing Salmeterol/Fluticasone Easyhaler Products and Seretide Diskus (NCT02162485) · Clinical Trials Directory