Study identifier:D3180C00009
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Randomized, Single-blind, Placebo-Controlled, Single-Centre Phase I Study to Assess the Safety, Tolerability and Pharmacokinetics after Single Ascending Oral Doses of AZD2207 in Japanese Healthy Male Subjects
obesity
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
Arms | Assigned Interventions |
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