A randomized, single-center, open-label, two-period cross-over, pharmacokinetic study, to evaluate the bioequivalence of a single 40 mg H 199/18 dose administered as an intact capsule and as an open capsule in healthy male and female volunteers.
Study identifier:SH-QBE-0068
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Study Complete
Official Title
A randomized, single-center, open-label, two-period cross-over, pharmacokinetic study, to evaluate the bioequivalence of a single 40 mg H 199/18 dose administered as an intact capsule and as an open capsule in healthy male and female volunteers.
Medical condition
gastrointestinal diseases
Phase
N/A
Healthy volunteers
-
Study drug
-
Sex
-
Actual Enrollment
-
Study type
Interventional
Age
-
Date
Study Start Date: 01 Jan 1971
Primary Completion Date: -
Study Completion Date: -
Study design
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verification:
Verified 01 Nov 2013 by AstraZeneca
Sponsors
AstraZeneca
Collaborators
-
Inclusion and exclusion criteria
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