Single Oral Dose of 60 mg [14C]AZD9668 in Healthy Male Volunteers
NCT ID: NCT01147549
Last Updated: 2010-12-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
4 participants
INTERVENTIONAL
2010-06-30
2010-07-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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1
\[C14\]AZD9668
[C14]AZD9668
Oral Solution 60 mg Single Dose
Interventions
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[C14]AZD9668
Oral Solution 60 mg Single Dose
Eligibility Criteria
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Inclusion Criteria
* Have a body mass index (BMI) between 18 and 30 kg/m2 and weigh at least 50 kg
Exclusion Criteria
* History or presence of any clinically significant disease or disorder in the opinion of the investigator
* Any clinically relevant abnormal findings in physical examination, clinical chemistry, haematology, urinalysis, vital signs or ECG at baseline in the opinion of the investigator
50 Years
MALE
Yes
Sponsors
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AstraZeneca
INDUSTRY
Responsible Party
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AstraZeneca
Principal Investigators
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Chris O'Brien
Role: STUDY_DIRECTOR
AstraZeneca R&D, Wilmington
Tim Mant, Professor
Role: PRINCIPAL_INVESTIGATOR
Quintiles Drug Research Unit, United Kingdom
Locations
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Research Site
London, , United Kingdom
Countries
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Other Identifiers
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D0520C00016
Identifier Type: -
Identifier Source: org_study_id