A Phase II Trial of Calcitriol and Naproxen in Patients With Recurrent Prostate Cancer
Primary Purpose
Prostatic Neoplasms, Prostate Cancer
Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Calcitriol
Naproxen-n-butyl nitrate
Sponsored by

About this trial
This is an interventional treatment trial for Prostatic Neoplasms
Eligibility Criteria
Inclusion Criteria:
- Must give written informed consent
- Histologically confirmed adenocarcinoma of the prostate
- Biochemical relapse after primary radiation therapy or surgery
- Normal testosterone levels
- 3 rising PSA after nadir, with interval between PSA determinations > 2 weeks
Exclusion Criteria:
- Local recurrence by CT scan
- Distant metastases by bone scan
- Hypercalcemia
- Nephrolithiasis
- Renal insufficiency (serum creatinine > 1.8 mg/dl)
- Pancreatitis
- History of ulcer or gastrointestinal bleeding
- More than 6 months of hormone ablation therapy
- Concurrent therapy for prostate cancer
- Uncontrolled HTN
- H/O MI, CVA, TIA
- Known coronary disease/cerebrovascular disease
- Platelet counts <50
- Patients on anticoagulants
- Patients on lithium
Sites / Locations
- Stanford University School of Medicine
Outcomes
Primary Outcome Measures
PSA response - 50% PSA decline, PSA progression, PSA response duration, progressive disease, time to PSA progression.
Secondary Outcome Measures
Progressive disease in this study's patients, who would be treated with calcitriol and naprosyn, will be compared to that in historical controls of patients treated with calcitriol alone.
Full Information
NCT ID
NCT00383487
First Posted
September 29, 2006
Last Updated
January 25, 2013
Sponsor
Stanford University
Collaborators
Novacea
1. Study Identification
Unique Protocol Identification Number
NCT00383487
Brief Title
A Phase II Trial of Calcitriol and Naproxen in Patients With Recurrent Prostate Cancer
Official Title
A Phase II Trial of Calcitriol and Naproxen in Patients With Recurrent Prostate Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
January 2013
Overall Recruitment Status
Terminated
Why Stopped
Extreme toxicity
Study Start Date
March 2005 (undefined)
Primary Completion Date
July 2007 (Actual)
Study Completion Date
July 2007 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University
Collaborators
Novacea
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To determine whether, in this patient population, treatment with calcitriol and Naproxen is more effective in delaying the growth of prostate cancer than treatment with calcitriol alone as seen in historical controls.
Detailed Description
In summary, in vitro and in vivo studies, as well as early phase clinical trial, have shown a promising role for both calcitriol and NSAIDs in the treatment of prostate cancer. Moreover, calcitriol and NSAIDs both exert their antiproliferative effect by decreasing prostaglandin levels, but they do so by different mechanisms. Thus, there is reason to believe that their combined effects on prostaglandins may be synergistic. Preliminary in vitro assays in which calcitriol is given in combination with one of two different NSAIDs (Naprosyn or sulindac) to LNCaP cell lines have indicated such synergy. This observation provides the rational for using them in combination for the treatment of prostate cancer. In addition, it is hoped that any synergy noted would allow for the use of lower doses of NSAIDs.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostatic Neoplasms, Prostate Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Calcitriol
Other Intervention Name(s)
1,25-Dihydroxycholecalciferol, 1,25-dihydroxyvitamin D3
Intervention Description
0.5 micrograms/kilogram q weekly
Intervention Type
Drug
Intervention Name(s)
Naproxen-n-butyl nitrate
Other Intervention Name(s)
Naprosyn
Intervention Description
400 mg BID, oral
Primary Outcome Measure Information:
Title
PSA response - 50% PSA decline, PSA progression, PSA response duration, progressive disease, time to PSA progression.
Secondary Outcome Measure Information:
Title
Progressive disease in this study's patients, who would be treated with calcitriol and naprosyn, will be compared to that in historical controls of patients treated with calcitriol alone.
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Must give written informed consent
Histologically confirmed adenocarcinoma of the prostate
Biochemical relapse after primary radiation therapy or surgery
Normal testosterone levels
3 rising PSA after nadir, with interval between PSA determinations > 2 weeks
Exclusion Criteria:
Local recurrence by CT scan
Distant metastases by bone scan
Hypercalcemia
Nephrolithiasis
Renal insufficiency (serum creatinine > 1.8 mg/dl)
Pancreatitis
History of ulcer or gastrointestinal bleeding
More than 6 months of hormone ablation therapy
Concurrent therapy for prostate cancer
Uncontrolled HTN
H/O MI, CVA, TIA
Known coronary disease/cerebrovascular disease
Platelet counts <50
Patients on anticoagulants
Patients on lithium
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Sandy Srinivas
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanford University School of Medicine
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States
12. IPD Sharing Statement
Learn more about this trial
A Phase II Trial of Calcitriol and Naproxen in Patients With Recurrent Prostate Cancer
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