search
Back to results

Use of Celecoxib in Patients With Intraductal Papillary Mucinous Neoplasms (IPMNs)

Primary Purpose

Pancreas Neoplasms

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
COX-2 Inhibitor 6-8 weeks prior to surgery
COX-2 Inhibitor for 6 months prior to follow-up EUS or ERCP
Sponsored by
Indiana University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pancreas Neoplasms focused on measuring celecoxib for pancreas lesions

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Clinical diagnosis of IPMN ECOG Performance status of 0, 1, or 2 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 the last month 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

Sites / Locations

  • Indiana University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Surgical Candidate

Medical Candidate

Arm Description

COX-2 Inhibitor 6-8 weeks prior to surgery

COX-2 Inhibitor for 6 months prior to follow-up EUS or ERCP

Outcomes

Primary Outcome Measures

Concentration of PGE2 in Urine at Baseline, Surgery, 1 wk, 4wks, and 6 Months
Measured by Elisa at participant level - only participant level data available; not summarized across group
Concentration of PGE2 in Serum at Baseline, Surgery, 1 wk, 4wks, and 6 Months
Measured by Elisa at participant level - only participant level data available; not summarized across group
Concentration of PGEM in Urine at Baseline, Surgery, 1 wk, 4wks, and 6 Months
Measured by Elisa at participant level - only participant level data available; not summarized across group
Concentration of PGEM in Serum at Baseline, Surgery, 1 wk, 4wks, and 6 Months
Measured by Elisa at participant level - only participant level data available; not summarized across group

Secondary Outcome Measures

Number of Participants With Clinical Changes in IPMN Progression.
Examine the short term effect of celecoxib on clinical progression of IPMN in the surgical arm; Examine the long term effect of celecoxib on clinical progression of IPMN in the medical arm.

Full Information

First Posted
September 12, 2005
Last Updated
February 26, 2016
Sponsor
Indiana University School of Medicine
search

1. Study Identification

Unique Protocol Identification Number
NCT00198081
Brief Title
Use of Celecoxib in Patients With Intraductal Papillary Mucinous Neoplasms (IPMNs)
Official Title
A Phase II Trial of Celecoxib in Patients With IPMN
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Terminated
Why Stopped
Lack of funding and personnel to conduct study.
Study Start Date
September 2005 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
April 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Indiana University School of Medicine

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreas Neoplasms
Keywords
celecoxib for pancreas lesions

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
8 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Surgical Candidate
Arm Type
Experimental
Arm Description
COX-2 Inhibitor 6-8 weeks prior to surgery
Arm Title
Medical Candidate
Arm Type
Experimental
Arm Description
COX-2 Inhibitor for 6 months prior to follow-up EUS or ERCP
Intervention Type
Drug
Intervention Name(s)
COX-2 Inhibitor 6-8 weeks prior to surgery
Other Intervention Name(s)
Celecoxib
Intervention Description
400 mg BID 6-8 weeks prior to surgery
Intervention Type
Drug
Intervention Name(s)
COX-2 Inhibitor for 6 months prior to follow-up EUS or ERCP
Other Intervention Name(s)
Celecoxib
Intervention Description
400 mg BID for 6 months prior to follow-up EUS or ERCP
Primary Outcome Measure Information:
Title
Concentration of PGE2 in Urine at Baseline, Surgery, 1 wk, 4wks, and 6 Months
Description
Measured by Elisa at participant level - only participant level data available; not summarized across group
Time Frame
Baseline, surgery, 1 wk, 4 wks, and 6 months
Title
Concentration of PGE2 in Serum at Baseline, Surgery, 1 wk, 4wks, and 6 Months
Description
Measured by Elisa at participant level - only participant level data available; not summarized across group
Time Frame
Baseline, surgery, 1 wk, 4 wks, and 6 months
Title
Concentration of PGEM in Urine at Baseline, Surgery, 1 wk, 4wks, and 6 Months
Description
Measured by Elisa at participant level - only participant level data available; not summarized across group
Time Frame
Baseline, surgery, 1 wk, 4 wks, and 6 months
Title
Concentration of PGEM in Serum at Baseline, Surgery, 1 wk, 4wks, and 6 Months
Description
Measured by Elisa at participant level - only participant level data available; not summarized across group
Time Frame
Baseline, surgery, 1 wk, 4 wks, and 6 months
Secondary Outcome Measure Information:
Title
Number of Participants With Clinical Changes in IPMN Progression.
Description
Examine the short term effect of celecoxib on clinical progression of IPMN in the surgical arm; Examine the long term effect of celecoxib on clinical progression of IPMN in the medical arm.
Time Frame
Baseline, 6 months, 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of IPMN ECOG Performance status of 0, 1, or 2 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 the last month 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christian M. Schmidt, MD
Organizational Affiliation
Indiana University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Indiana University Hospital
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Use of Celecoxib in Patients With Intraductal Papillary Mucinous Neoplasms (IPMNs)

We'll reach out to this number within 24 hrs