Study identifier:D1520C05289
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A randomised, single-blind, placebo-controlled, single centre Phase I study to assess the safety, tolerability, pharmacokinetics, and pharmacodynamics of scending single oral doses of AZD9056 tablets in healthy Japanese male patients
Rheumatoid Arthritis
Phase 1
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Interventional
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Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Nov 2013 by AstraZeneca
AstraZeneca
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No locations available
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