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
|
Purpose
| 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
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
Inclusion Criteria:
- Clinical diagnosis of IPMN
- ECOG Performance status of 0 or 1
- Adequate liver function, bilirubin < 1.5 times ULN, ALT or AST < 2.5 times ULN
- Adequate renal function: creatinine < 1.8
- Must be at least 18
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
Indiana
Indiana University Hospital, Indianapolis, Indiana, 46202, United States
Sarah Dutkevitch, RN 317-274-5495 sdutkevi@iupui.edu
Christian M Schmidt, MD, Principal Investigator
Christian M. Schmidt, MD, Principal Investigator, Indiana University School of Medicine
More Information
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
- Celebrex (Drug Digest)
- Celebrex Consumer Information (U.S. Food and Drug Administration)

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