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
PHASE2
40 participants
INTERVENTIONAL
2003-08-31
2005-02-28
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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ABT-751
Eligibility Criteria
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Inclusion Criteria
* Recurrent tumor following treatment with irinotecan and/or oxaliplatin.
* Able to tolerate normal activities of daily living.
* Adequate bone marrow, kidney, and liver function.
Exclusion Criteria
* Anti-tumor therapy within 4 weeks of the start of ABT-751 administration.
* Prior radiation therapy.
* CNS metastasis.
18 Years
ALL
No
Sponsors
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Abbott
INDUSTRY
Principal Investigators
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Helen Eliopoulos, MD
Role: STUDY_DIRECTOR
Abbott
Locations
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University of Southern California
Los Angeles, California, United States
Cancer Institute Medical Group
Santa Monica, California, United States
Northwestern University
Chicago, Illinois, United States
University of Chicago Medical Center
Chicago, Illinois, United States
Duke University Medical Center
Durham, North Carolina, United States
University of Wisconsin Medical Center
Madison, Wisconsin, United States
Countries
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Other Identifiers
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M02-446
Identifier Type: -
Identifier Source: org_study_id