Study in healthy males to assess bioavailability of single fostamatinib with iv micro tracer dose

Study identifier:D4300C00027

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A Study to Assess the Absolute Bioavailability of a Single Oral Dose of Fostamatinib with Respect to an Intravenous Micro Tracer Dose of [14C] R406 in Healthy Male Volunteers

Medical condition

Healthy

Phase

Phase 1

Healthy volunteers

Yes

Study drug

Fostamatinib

Sex

Male

Actual Enrollment

10

Study type

Interventional

Age

18 Years - 55 Years

Date

Study Start Date: 01 Jul 2012
Primary Completion Date: 01 Aug 2012
Study Completion Date: 01 Aug 2012

Study design

Allocation: Non-randomized
Endpoint Classification: Pharmacokinetics Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Basic Science

Verification:

Verified 01 Jan 2014 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria