Study identifier:D4300C00026
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
An Open-Label, Non-Randomised, 2-Period, Single Centre Study to Assess the Pharmacokinetics of Digoxin in Healthy Subjects when Administered Alone and in Combination with Fostamatinib 100 mg Twice Daily
Healthy Volunteers, Rheumatoid Arthritis
Phase 1
Yes
Digoxin, Fostamatinib
All
21
Interventional
18 Years - 45 Years
Allocation: Non-randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Basic Science
Verified 01 Jan 2014 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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The purpose of this study is to investigate the drug interaction between fostamatinib and digoxin by comparing the safety, tolerability and plasma concentration of digoxin when administered alone and with fostamatinib in healthy subjects.
Location
Location
London, United Kingdom
Arms | Assigned Interventions |
---|---|
Experimental: 1 Digoxin | Drug: Digoxin oral tablets, 0.25mg bd on Day 1 and 0.25 Once daily from Day 2 to 15 |
Experimental: 2 Fostamatinib | Drug: Digoxin oral tablets, 0.25mg bd on Day 1 and 0.25 Once daily from Day 2 to 15 Drug: Fostamatinib oral tablets, 100mg (2 X 50mg) bd from Day 9 - 15 |
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