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Use of Celecoxib in Patients with Intraductal Papillary Mucinous Neoplasms (IPMNs) - Article


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Celecoxib

Celebrex 




Clinical Trial: Use of Celecoxib in Patients with Intraductal Papillary Mucinous Neoplasms (IPMNs)

This study is not yet open for patient recruitment.
Verified by Indiana University School of Medicine September 2005

Sponsors and Collaborators: Indiana University School of Medicine
Pfizer
Information provided by: Indiana University School of Medicine
ClinicalTrials.gov Identifier: NCT00198081

Purpose

The purpose of the study is to find out whether the drug celecoxib has beneficial effects on people with pre-cancerous lesions of the pancreas.
Condition Intervention Phase
Pancreas Neoplasms
 Drug: celecoxib
Phase II

MedlinePlus related topics:  Pancreatic Cancer

Study Type: Interventional
Study Design: Prevention, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study

Official Title: A Phase II Trial of Celecoxib in Patients With IPMN

Further Study Details: 
Primary Outcomes: Determine whether the COX-2 inhibitor celecoxib changes the IPMN tumor marker profile in serum, pancreatic fluid and tissue of patients with IPMN through gene and protein expression profiling studies.
Secondary Outcomes: Determine whether the COX-2 inhibitor celecoxib changes IPMN progression clinically.
Expected Total Enrollment:  30

Study start: September 2005

Efforts at finding a successful chemotherapy for pancreatic cancer have been disappointing. Some patients are at increased risk of pancreatic cancer or may have pre-malignant pancreatic lesions which predispose them to later pancreatic cancer development. In these individuals, chemopreventative measures may block future development of pancreatic cancer. Human tissue studies, cell culture and animal models of pancreatic cancer strongly suggests that cyclooxygenase-2 (COX-2) may be a successful target for chemoprevention. COX-2 is overexpressed in human pancreatic cancers. Elevated COX-2 expression correlates with progression of premalignant precursors of pancreatic cancer in development models of hamster pancreatic cancer. Human tissue studies confirm increases in COX-2 expression with progression of premalignant precursors called intraductal papillary mucinous neoplasms (IPMNs) and pancreatic intraepithelial neoplasms (PanINs). Moreover, COX-2 inhibitors appear to have chemopreventative efficacy in the PC-1 homograft model of hamster pancreatic cancer. Demographic studies have suggested COX-2 inhibitors may confer protection from pancreatic cancer. We propose to conduct a pilot/phase II trial to determine the chemopreventative effects of the COX-2 inhibitor celecoxib in patients with premalignant pancreatic lesions.

Patients registered to the study will take celecoxib twice daily for 6-8 weeks prior to surgery (if patient decides to have surgery for his/her condition). If subject is not a surgical candidate or puts off surgical treatment, subject will take celecoxib for 6 months.

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

Exclusion Criteria:

  • Use of COX-2 selective inhibitors within last 3 months
  • More than occasional use of NSAIDS in last month (occasional use defined as up to twice weekly dosing)
  • CA19-9 levels 1.5 times the ULN
  • Active pancreatitis
  • Taking sulphonylureas, fluconazole or lithium concomitantly

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00198081

Christian M. Schmidt, MD      (317) 278-8349    maxschmi@iupui.edu

Indiana
      Indiana University Hospital, Indianapolis,  Indiana,  46202,  United States
Christian M. Schmidt, MD  317-278-8349    maxschmi@iupui.edu 
Sarah Dutkevitch, RN  317-274-5495    sdutkevi@iupui.edu 
Christian M Schmidt, MD,  Principal Investigator

Study chairs or principal investigators

Christian M. Schmidt, MD,  Principal Investigator,  Indiana University School of Medicine   

More Information

Study ID Numbers:  0305-20
Last Updated:  September 19, 2005
Record first received:  September 12, 2005
ClinicalTrials.gov Identifier:  NCT00198081
Health Authority: United States: Institutional Review Board
ClinicalTrials.gov processed this record on 2005-09-20

Resources



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Page Updated: September 6, 2005
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