Investigational Agent AG-013736 In Combinations With Standard Of Care Treatments For Patient's With Advanced Solid Tumor
Completed · Phase 1
Conditions studied: Neoplasms
In brief
To determine the best dose of this investigational agent AG-013736 in combination with various standard of care treatments for advanced solid tumors.
Key facts
- Study ID
- NCT00454649
- Run by
- Pfizer
- People needed
- 102
- Starts
- 2005-12-01
- Expected to finish
- 2011-04-01
- Last updated by the study team
- 2012-04-04
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Advanced solid tumors suitable for treatment with Taxanes, with or without carboplatin, or treatment with Capecitabine, Gemcitabine/Cisplatin. or Pemetrexed/Cisplatin
You may not qualify if…
- Tumors abutting or providing support for blood vessels
- Any significant gastrointestinal abnormalities or active bleeding.
Where it is running
- Pfizer Investigational Site — Augusta, Georgia, United States
- Pfizer Investigational Site — Augusta, Georgia, United States
- Pfizer Investigational Site — Harvey, Illinois, United States
- Pfizer Investigational Site — Harvey, Illinois, United States
- Pfizer Investigational Site — Tinley Park, Illinois, United States
- Pfizer Investigational Site — Hobart, Indiana, United States
- Pfizer Investigational Site — Munster, Indiana, United States
- Pfizer Investigational Site — Philadelphia, Pennsylvania, United States
- Pfizer Investigational Site — Houston, Texas, United States
- Pfizer Investigational Site — Kennewick, Washington, United States
- Pfizer Investigational Site — Warsaw, Poland
- Pfizer Investigational Site — Barcelona, Barcelona, Spain
- Pfizer Investigational Site — Madrid, Madrid, Spain
Full record on ClinicalTrials.gov
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