Phase I, Open-Label, Dose-Escalation Study of AZD4877 in Solid Tumors
NCT ID: NCT00389389
Last Updated: 2009-05-01
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
75 participants
INTERVENTIONAL
2006-09-30
2008-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Interventions
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AZD4877
intravenous infusion
Eligibility Criteria
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Inclusion Criteria
* Relatively good overall health other than your cancer.
Exclusion Criteria
* Serious heart conditions.
* Poor liver or kidney function.
18 Years
ALL
No
Sponsors
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AstraZeneca
INDUSTRY
Principal Investigators
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Judith Ochs, MD
Role: STUDY_DIRECTOR
AstraZeneca
Locations
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Research Site
Denver, Colorado, United States
Research Site
Nashville, Tennessee, United States
Research Site
Houston, Texas, United States
Countries
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Other Identifiers
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D2782C00001
Identifier Type: -
Identifier Source: org_study_id
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