A Safety And Pharmacokinetic Study With CVX-045 In Patients With Advanced Solid Tumors
NCT ID: NCT00879554
Last Updated: 2010-12-13
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
2007-02-28
2010-11-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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1
CVX-045
Weekly, intravenous dose
Interventions
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CVX-045
Weekly, intravenous dose
Eligibility Criteria
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Inclusion Criteria
* Adequate coagulation, liver and renal function.
* Candidate for DCE-MRI evaluation.
* ECOG (Eastern Cooperative Oncology Group) performance status 0 or 1.
Exclusion Criteria
* Uncontrolled hypertension.
* Certain gastrointestinal problems including fistula and abscess.
* Patients with primary brain cancer.
18 Years
ALL
No
Sponsors
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Pfizer
INDUSTRY
Responsible Party
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Pfizer, Inc.
Principal Investigators
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Pfizer CT.gov Call Center
Role: STUDY_DIRECTOR
Pfizer
Locations
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Pfizer Investigational Site
Scottsdale, Arizona, United States
Pfizer Investigational Site
Santa Monica, California, United States
Pfizer Investigational Site
Philadelphia, Pennsylvania, United States
Countries
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Related Links
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To obtain contact information for a study center near you, click here.
Other Identifiers
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B1121003
Identifier Type: -
Identifier Source: org_study_id