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
INTERVENTIONAL
2005-08-31
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
TREATMENT
NONE
Interventions
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XL820
Eligibility Criteria
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Inclusion Criteria
* Cancer for which standard therapies do not exist or are no longer effective
* Life expectancy of \> 3 months
* Adequate bone marrow, liver, and kidney function
* Willing to use accepted method of contraception during the course of the study
* Negative pregnancy test (females)
* Written informed consent
Exclusion Criteria
* Radiotherapy to more than 25% of bone marrow within 4 weeks of the start of treatment
* Investigational drug within 30 days of the start of treatment
* Subjects with known brain metastasis
* Uncontrolled medical disorder such as infection or cardiovascular disease
* Subjects known to be HIV positive
* Pregnant or breastfeeding women
18 Years
ALL
No
Sponsors
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Exelixis
INDUSTRY
Locations
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The Cancer Institute of New Jersey
New Brunswick, New Jersey, United States
Cancer Therapy and Research Center
San Antonio, Texas, United States
Countries
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Other Identifiers
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XL820-001
Identifier Type: -
Identifier Source: org_study_id