A Study Of Sunitinib Compared To Placebo For Patients With Advanced Pancreatic Islet Cell Tumors
Stopped early · Phase 3 · Has a placebo group
Conditions studied: Carcinoma, Islet Cell, Carcinoma, Pancreas
In brief
This study randomized patients with advanced pancreatic islet cell tumors to receive either sunitinib or placebo. Patients who were randomized to sunitinib received 37.5 mg of sunitinib daily, those randomized to placebo received a tablet that looked similar but had no active drug. Neither the patient or the doctor knew whether the patient was receiving sunitinib or placebo. Patients were followed to determine the status and size of their tumors, survival, quality of life and safety of the drug. The study was designed to detect a 50% improvement in median PFS\[Progression Free Survival\] with 90% power and was to enroll 340 subjects. An interim analysis was planned when 130 events had occurred, and the final analysis was to be conducted when 260 events had occurred. Study A6181111 was stopped early during the enrollment period because of a clear and clinically meaningful improvement in efficacy for the sunitinib treatment arm as recommended by the DMC \[Data Monitoring Committee\]. The actual number of subjects enrolled was 171 and the actual number of PFS events recorded was 81 PFS events. The decision to terminate the study was not based on safety concerns related to sunitinib administration.
Key facts
- Study ID
- NCT00428597
- Run by
- Pfizer
- People needed
- 171
- Starts
- 2007-06-01
- Expected to finish
- 2009-04-01
- Last updated by the study team
- 2010-10-11
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Well-differentiated advanced/metastatic pancreatic islet cell tumor
- Tumor has shown progression within the past year.
You may not qualify if…
- Current treatment with any chemotherapy, chemoembolization therapy, immunotherapy, or investigational anticancer agent other than somatostatin analogues
- Prior treatment with any tyrosine kinase inhibitors or anti-VEGF[Vascular endothelial growth factor] angiogenic inhibitors.
- Prior treatment with non-VEGF-targeted angiogenic inhibitors is permitted
Where it is running
- Pfizer Investigational Site — Iowa City, Iowa, United States
- Pfizer Investigational Site — Worcester, Massachusetts, United States
- Pfizer Investigational Site — Worcester, Massachusetts, United States
- Pfizer Investigational Site — City of Saint Peters, Missouri, United States
- Pfizer Investigational Site — Creve Coeur, Missouri, United States
- Pfizer Investigational Site — St Louis, Missouri, United States
- Pfizer Investigational Site — St Louis, Missouri, United States
- Pfizer Investigational Site — Austin, Texas, United States
- Pfizer Investigational Site — Austin, Texas, United States
- Pfizer Investigational Site — Austin, Texas, United States
- Pfizer Investigational Site — Austin, Texas, United States
- Pfizer Investigational Site — Georgetown, Texas, United States
- Pfizer Investigational Site — Norfolk, Virginia, United States
- Pfizer Investigational Site — Perth, Western Australia, Australia
- Pfizer Investigational Site — Brussels, Belgium
- Pfizer Investigational Site — Brussels, Belgium
- Pfizer Investigational Site — Leuven, Belgium
- Pfizer Investigational Site — Vancouver, British Columbia, Canada
- Pfizer Investigational Site — Halifax, Nova Scotia, Canada
- Pfizer Investigational Site — Halifax, Nova Scotia, Canada
- Pfizer Investigational Site — Halifax, Nova Scotia, Canada
- Pfizer Investigational Site — Toronto, Ontario, Canada
- Pfizer Investigational Site — Montreal, Quebec, Canada
- Pfizer Investigational Site — Montreal, Quebec, Canada
- Pfizer Investigational Site — Aurora, Colorado, United States
Full record on ClinicalTrials.gov
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