Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Healthy Volunteers
Type
Interventional
Phase
Phase 1
Design
Allocation: RandomizedIntervention Model: Crossover AssignmentIntervention Model Description: The study is a 2-part 4-period crossover study where the study subjects participate either in part 1 (20 subjects) or in part 2 (20 subjects). Parts can run in sequence or parallel. All study subjects receive single dose of Tiotropium Easyhaler on 3 periods and Spiriva HandiHaler on 1 period.Masking: None (Open Label)Masking Description: Bioanalytical laboratory will be blinded with regard to the sequence of the product administration.Primary Purpose: Basic Science

Participation Requirements

Age
Between 18 years and 60 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04850144
Collaborators
Not Provided
Investigators
Study Director: Orion Corporation Clinical Study Director Orion Corporation, Orion Pharma