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Spots Global Cancer Trial Database for 3-AP and Gemcitabine in Treating Patients With Unresectable or Metastatic Pancreatic Cancer

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Trial Identification

Brief Title: 3-AP and Gemcitabine in Treating Patients With Unresectable or Metastatic Pancreatic Cancer

Official Title: A Phase II Study of Triapine in Combination With Gemcitabine in Patients With Pancreatic Cancer

Study ID: NCT00064051

Study Description

Brief Summary: RATIONALE: Drugs used in chemotherapy such as gemcitabine use different ways to stop tumor cells from dividing so they stop growing or die. 3-AP may stop the growth of tumor cells by blocking the enzymes necessary for tumor cell growth and may help gemcitabine kill more cancer cells by making them more sensitive to the drug. PURPOSE: This phase II trial is studying how well giving gemcitabine together with 3-AP works in treating patients with unresectable or metastatic pancreatic cancer.

Detailed Description: OBJECTIVES: * Determine the objective response rate (partial and complete response) in patients with unresectable or metastatic pancreatic cancer treated with 3-AP and gemcitabine. * Determine the progression-free interval and survival of patients treated with this regimen. * Determine the safety and feasibility of this regimen in these patients. OUTLINE: This is a multicenter study. * Stage I: Patients receive 3-AP IV over 4 hours and gemcitabine IV over 30 minutes on days 1, 8, and 15. Treatment repeats every 4 weeks for up to 12 courses in the absence of disease progression or unacceptable toxicity. * Stage II: Patients receive a higher dose of 3-AP IV continuously over 24 hours on days 1, 8, and 15. Within 1 hour of completing 3-AP administration, patients receive gemcitabine IV over 30 minutes on days 2, 9, and 16. Treatment repeats every 4 weeks for up to 12 courses in the absence of disease progression or unacceptable toxicity. Patients are followed at 1 month, every 2 months for 6 months, and then every 3 months for 18 months. PROJECTED ACCRUAL: A total of 50-95 patients will be accrued for this study within 18-24 months.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Chicago Cancer Research Center, Chicago, Illinois, United States

Indiana Oncology Hematology Consultants, Indianapolis, Indiana, United States

University of Minnesota Cancer Center, Minneapolis, Minnesota, United States

Sarah Cannon Cancer Center at Centennial Medical Center, Nashville, Tennessee, United States

Universitair Ziekenhuis Gent, Ghent, , Belgium

Christie Hospital N.H.S. Trust, Manchester, England, United Kingdom

Royal Marsden NHS Foundation Trust - Surrey, Sutton, England, United Kingdom

Contact Details

Name: Mario Sznol, MD

Affiliation: Vion Pharmaceuticals

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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