Effects of cimetidine repeated oral dose 400 mg twice-daily co-administration on the pharmacokinetics of roflumilast and roflumilast-N-oxide
Study identifier:BY217/CP-041
ClinicalTrials.gov identifier:N/A
EudraCT identifier:2005-005220-13
CTIS identifier:N/A
Study Complete
Official Title
*Please Note* The Study you are attempting to view was acquired from Takeda by AstraZeneca and was disclosed initially by Takeda per their Transparency Policies. More information regarding this study may be available by contacting [email protected].
Medical condition
Chronic Obstructive Pulmonary Disease
Phase
Phase 1
Healthy volunteers
Yes
Study drug
-
Sex
All
Actual Enrollment
16
Study type
Interventional
Age
18 Years - 45 Years
Date
Study Start Date: 01 Mar 2006
Primary Completion Date: -
Study Completion Date: 01 May 2006
Study design
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verification:
Verified 01 Jun 2016 by Takeda
Sponsors
Takeda
Collaborators
-
Inclusion and exclusion criteria
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