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A Phase II Study of Sunitinib Malate (SU11248, NSC #736511, IND #74,019) in Patients With Previously Treated Pancreatic Adenocarcinoma With Measurable Metastatic Disease Following Progression on Front-Line Gemcitabine-Based Therapy
This phase II trial is studying how well sunitinib works in treating patients with metastatic pancreatic cancer that progressed after first-line therapy with gemcitabine. Sunitinib may stop the growth of pancreatic cancer by blocking blood flow to the tumor and by blocking some of the enzymes needed for cell growth.
PRIMARY OBJECTIVES: I. To determine the response rate to sunitinib malate in patients with previously treated metastatic pancreatic adenocarcinoma. SECONDARY OBJECTIVES: I. To determine the duration of response, progression-free survival and overall survival of sunitinib malate in patients with previously treated metastatic pancreatic adenocarcinoma. II. To determine the safety of sunitinib malate in patients with previously treated metastatic pancreatic adenocarcinoma. OUTLINE: This is a multicenter, nonrandomized study. Patients receive oral sunitinib malate daily on days 1-28. Treatment repeats every 6 weeks in the absence of disease progression or unacceptable toxicity. After completion of study, patients are followed every 3 months until 2 years from study entry or until disease progression.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Cancer and Leukemia Group B
Chicago, Illinois, United States
Memorial Sloan Kettering Cancer Center
New York, New York, United States
Start Date
November 1, 2006
Primary Completion Date
September 1, 2007
Last Updated
June 4, 2013
64
ACTUAL participants
sunitinib malate
DRUG
Lead Sponsor
National Cancer Institute (NCI)
NCT07098598
NCT01835041
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