Study Evaluating TTI-237 in Advanced Malignant Solid Tumors.
NCT ID: NCT00195325
Last Updated: 2007-03-26
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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TERMINATED
PHASE1
45 participants
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
FACTORIAL
ECT
NONE
Interventions
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TTI-237
Eligibility Criteria
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Inclusion Criteria
* Life expectancy of at least 12 weeks
* ECOG (The Eastern Cooperative Oncology Group scale) performance status of 0, 1, or 2
Exclusion Criteria
* History of any other prior malignancy within the last 5 years
18 Years
ALL
No
Sponsors
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Wyeth is now a wholly owned subsidiary of Pfizer
INDUSTRY
Principal Investigators
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Medical Monitor
Role: STUDY_DIRECTOR
Wyeth is now a wholly owned subsidiary of Pfizer
Locations
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Lexington, Kentucky, United States
Cleveland, Ohio, United States
Nashville, Tennessee, United States
Countries
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Other Identifiers
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3162K1-100
Identifier Type: -
Identifier Source: org_study_id
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