A Safety And Pharmacokinetic Study With CVX-045 In Patients With Advanced Solid Tumors
Completed · Phase 1
Conditions studied: Advanced Solid Tumors, Neoplasms, Carcinoma, Cancer, Malignancy
In brief
The purpose of the study is to determine safety and tolerability of CVX-045 in patients with advanced solid tumors.
Key facts
- Study ID
- NCT00879554
- Run by
- Pfizer
- People needed
- 40
- Starts
- 2007-02-01
- Expected to finish
- 2010-11-01
- Last updated by the study team
- 2010-12-13
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Confirmed advanced solid tumors unresponsive to currently available therapies, or for which there is no standard therapy.
- Adequate coagulation, liver and renal function.
- Candidate for DCE-MRI evaluation.
- ECOG (Eastern Cooperative Oncology Group) performance status 0 or 1.
You may not qualify if…
- Evidence of bleeding problems.
- Uncontrolled hypertension.
- Certain gastrointestinal problems including fistula and abscess.
- Patients with primary brain cancer.
Where it is running
- Pfizer Investigational Site — Scottsdale, Arizona, United States
- Pfizer Investigational Site — Santa Monica, California, United States
- Pfizer Investigational Site — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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