Study identifier:D1710C00019
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
An Open-label, Randomized, 4 Period Crossover, Replicate Study to Assess the Relative Bioavailability of the Phase III and Phase IIb Formulations of AZD5672 in Healthy Male and Female Subjects
Rheumatoid Arthritis
Phase 1
Yes
AZD5672
All
24
Interventional
18 Years - 55 Years
Allocation: Randomized
Endpoint Classification: Bio-availability Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Other
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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The aim of this study is to compare the blood levels achieved with a new formulation of AZD5672 to an existing formulation of AZD5672 used in previous studies
Location
Location
Manchester, United Kingdom
Arms | Assigned Interventions |
---|---|
Experimental: 1 40 or 100mg AZD5672, Reference formulation | Drug: AZD5672 40 mg tablet (Reference formulation) Drug: AZD5672 100 mg (2 x 50 mg tablet (Reference Formulation) |
Experimental: 2 40 or 100mg AZD5672, Test formulation | Drug: AZD5672 40 mg tablet (Test formulation) Drug: AZD5672 100 mg tablet (Test formulation) |
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