Study to Investigate Safety and Tolerability Single Ascending Doses of AZD4017
NCT ID: NCT00791752
Last Updated: 2009-06-16
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
40 participants
INTERVENTIONAL
2008-11-30
2009-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
SINGLE
Study Groups
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1
AZD4017 in ascending doses (start dose 2mg)
AZD4017
ascending single doses (start dose 2 mg), oral suspension
2
Placebo
Placebo
Placebo
Interventions
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AZD4017
ascending single doses (start dose 2 mg), oral suspension
Placebo
Placebo
Eligibility Criteria
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Inclusion Criteria
* BMI between 19 and 30 kg/m2
* Subjects must be willing to use barrier methods of contraception
Exclusion Criteria
* Any clinically significant illness, medical/surgical procedure or trauma within 4 weeks of the first administration of investigational product
* History or presence of gastrointestinal, hepatic or renal disease or any other condition known to interfere with absorption, distribution, metabolism or excretion of drugs
* Laboratory blood sample result showing elevated liverenzymes (ASAT, ALAT) and muscle enzymes (CK).
18 Years
45 Years
MALE
Yes
Sponsors
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AstraZeneca
INDUSTRY
Responsible Party
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AstraZeneca R&D Mölndal, Sweden
Principal Investigators
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Marianne Hartford, MD PhD
Role: PRINCIPAL_INVESTIGATOR
Sahlgrenska University Sweden
Locations
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Research Site
Gotteborg, , Sweden
Countries
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Other Identifiers
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D2060C00001
Identifier Type: -
Identifier Source: org_study_id
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