Study identifier:D4300C00010
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
An Open-label, Single-center Study to Assess the Pharmacokinetics of R406 in Subjects with Hepatic Impairment and in Healthy Subjects Following Administration of a Single Dose of Fostamatinib Disodium 150 mg
Hepatic Impairment, Healthy Volunteers, Amount of R406 in blood
Phase 1
Yes
Fostamatinib
All
32
Interventional
18 Years +
Allocation: Non-randomized
Endpoint Classification: Pharmacokinetics Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Basic Science
Verified 01 Apr 2014 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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No locations available
Arms | Assigned Interventions |
---|---|
Experimental: 1 Mild hepatic impairment | Drug: Fostamatinib Oral tablets, single dose |
Experimental: 2 Moderate hepatic impairment | Drug: Fostamatinib Oral tablets, single dose |
Experimental: 3 Severe hepatic impairment | Drug: Fostamatinib Oral tablets, single dose |
Experimental: 4 Matched healthy volunteers with normal hepatic function | Drug: Fostamatinib Oral tablets, single dose |