Study Of SU011248 In Combination With Docetaxel In Patients With Advanced Cancer
Completed · Phase 1
Conditions studied: Advanced Solid Tumors, Non Small Cell Lung Cancer
In brief
This study is determining the maximum tolerated dose and safety of SU011248 (sunitinib malate, SUTENT) in combination with docetaxel (Taxotere). Several dosing regimens will be tested in patients with advanced solid tumors, including non small cell lung cancer.
Key facts
- Study ID
- NCT00712504
- Run by
- Pfizer
- People needed
- 49
- Starts
- 2004-07-01
- Expected to finish
- 2007-11-01
- Last updated by the study team
- 2008-11-11
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Advanced solid tumor malignancy ECOG 0 or 1
You may not qualify if…
- Prior treatment with with high-dose chemotherapy requiring stem cell rescue Prior irradiation to ≥25% of the bone marrow (e.g. whole pelvis=25%) Patients with centrally located lung lesions unless recently treated with radiotherapy
Where it is running
- Pfizer Investigational Site — Birmingham, Alabama, United States
- Pfizer Investigational Site — Birmingham, Alabama, United States
- Pfizer Investigational Site — Birmingham, Alabama, United States
- Pfizer Investigational Site — Nashville, Tennessee, United States
- Pfizer Investigational Site — Madison, Wisconsin, United States
Full record on ClinicalTrials.gov
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