Study identifier:D3550C00013
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I, Open-Label Study to Characterise the Absorption, Distribution, Metabolism and Excretion following a Single Oral Dose of [14C]AZD5069 in Healthy Male Volunteers
Healthy
Phase 1
Yes
[14C] AZD5069
Male
6
Interventional
50 Years +
Allocation: N/A
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Basic Science
Verified 01 Jun 2015 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: 1 [14C] AZD5069 | Drug: [14C] AZD5069 Single 120 mg oral dose administered on Day 1 |