A Randomized, open, single-dose, single centre, Phase I study to compare the relative bioavailability of two IR tablet formulations to a capsule formulation of AZD2207 after administration to healthy male and female subjects
Study identifier:D3180C00007
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Study Complete
Official Title
A Randomized, open, single-dose, single centre, Phase I study to compare the relative bioavailability of two IR tablet formulations to a capsule formulation of AZD2207 after administration to healthy male and female subjects
Medical condition
obesity
Phase
Phase 1
Healthy volunteers
-
Study drug
-
Sex
-
Actual Enrollment
-
Study type
Interventional
Age
-
Date
Study Start Date: 01 Aug 2007
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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