Drug/Agent Toxicity by Tissue/OrganPhase 3NCT00024427
Triacetyluridine and Fluorouracil Compared With Gemcitabine in Treating Patients With Unresectable Locally Advanced, or Metastatic Pancreatic Cancer
A Phase 3 study testing fluorouracil, gemcitabine hydrochloride and triacetyluridine in people with Drug/Agent Toxicity by Tissue/Organ and Pancreatic Cancer, run by Wellstat Therapeutics at 29 sites in 2 countries.
Trial summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Giving the drugs in different combinations may kill more tumor cells. Chemoprotective drugs such as triacetyluridine may protect normal cells from the side effects of chemotherapy. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Drug/Agent Toxicity by Tissue/Organ, Pancreatic Cancer
- What is being tested?
- fluorouracil, gemcitabine hydrochloride and triacetyluridine
- Type of treatment
- Pill or oral medicine
- How many people
- 250 participants
- Where
- 29 sitesin 2 countries
- Study dates
- Feb 2001to Feb 2006
- Phase
- Phase 3
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
DISEASE CHARACTERISTICS:
- Histologically or cytologically confirmed adenocarcinoma of the pancreas
- Unresectable locally advanced or metastatic disease
- Stage II, III, or IV
- Measurable or evaluable disease
- No elevated tumor marker (CA 19-9) only
- No clinically significant third-space fluid accumulation (e.g., ascites or pleural effusion)
- No carcinoid, islet cell, or lymphoma of the pancreas
- No prior or concurrent brain or leptomeningeal metastases
PATIENT CHARACTERISTICS:
Age:
- 18 and over
Performance status:
- Karnofsky 70-100%
Life expectancy:
- At least 3 months
Hematopoietic:
- WBC at least 3,500/mm^3
- Platelet count at least 100,000/mm^3
- Hemoglobin at least 9.5 g/dL
Hepatic:
- Bilirubin no greater than 2.0 mg/dL
- ALT or AST less than 3 times upper limit of normal (ULN) (5 times ULN if liver metastases present)
- No uncontrolled hepatic dysfunction
Renal:
- Creatinine less than 2.0 mg/dL
- No uncontrolled renal dysfunction
Cardiovascular:
- No uncontrolled cardiovascular disease requiring therapy, including the following:
- Angina
- Arrhythmias
- Uncompensated cardiac failure
- Myocardial infarction within the past 6 months
Pulmonary:
- No uncontrolled pulmonary dysfunction
Gastrointestinal:
- Able to take and/or retain oral medication
- No uncontrolled malabsorption syndrome or any other condition that would interfere with intestinal absorption
Other:
- No known allergy to fluorouracil (5-FU), gemcitabine, triacetyluridine, or any of their components
- No dihydropyrimidine-dehydrogenase deficiency
- No active uncontrolled infection
- No uncontrolled neurologic or psychiatric dysfunction
- No other malignancy except previously resected basal cell cancer or curatively resected stage I or less cervical cancer that has been disease free for at least 5 years
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- HIV negative
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- No concurrent biologic therapy (including immunotherapy) for cancer
Chemotherapy:
- No prior chemotherapy for cancer other than as a radiosensitizer
- No prior 5-FU or gemcitabine other than as a radiosensitizer
- No prior triacetyluridine
- No other concurrent chemotherapy (including leucovorin calcium) for cancer
Endocrine therapy:
- No concurrent hormonal therapy for cancer
- Concurrent megestrol, oral contraceptives, or postmenopausal estrogen replacement therapy allowed
Radiotherapy:
- Prior radiotherapy allowed
- No concurrent radiotherapy
Surgery:
- See Disease Characteristics
- Prior resection of pancreas allowed
Other:
- At least 30 days since prior investigational drug or therapeutic device
- No other concurrent anticancer therapy
- No other concurrent investigational drugs or devices
- No concurrent drugs that would interact adversely with 5-FU or gemcitabine
Trial locations and contacts
29 sites in 2 countries.
29 sites in 2 countries
United States26 sites
Summit Oncology Associates
Akron, Ohio, 44304
University of New Mexico Cancer Research and Treatment Center
Albuquerque, New Mexico, 87131-5636
Cancer Center at Greater Baltimore Medical Center
Baltimore, Maryland, 21204-6881
Brookwood Medical Center
Birmingham, Alabama, 35209-6804
Comprehensive Cancer Center at University of Alabama at Birmingham
Birmingham, Alabama, 35294
Providence Saint Joseph Medical Center - Burbank
Burbank, California, 91505
Northwest Oncology and Hematology Associates
Coral Springs, Florida, 33065
Corpus Christi Cancer Center
Corpus Christi, Texas, 78412
City of Hope Comprehensive Cancer Center
Duarte, California, 91010-3000
Florida Cancer Specialists - World Plaza
Fort Myers, Florida, 33908
Queens Medical Associates, PC
Fresh Meadows, New York, 11365
Wellstat Therapeutics
Gaithersburg, Maryland, 20878
Cancer Centers of the Carolinas - Eastside
Greenville, South Carolina, 29615
Penn State Cancer Institute at Milton S. Hershey Medical Center
Hershey, Pennsylvania, 17033-0850
Memorial Cancer Institute at Memorial Regional Hospital
Hollywood, Florida, 33021
Florida Oncology Associates - South Side
Jacksonville, Florida, 32207
Capitol Comprehensive Cancer Care Clinic
Jefferson City, Missouri, 65109
Scripps Cancer Center at Scripps Clinic
La Jolla, California, 92037
University of Miami Sylvester Comprehensive Cancer Center
Miami, Florida, 33136
Cancer Care Center
New Albany, Indiana, 47150
Florida Cancer Institute - New Port Richey
New Port Richey, Florida, 34655
New York Weill Cornell Cancer Center at Cornell University
New York, New York, 10021
Fox Chase - Temple Cancer Center
Philadelphia, Pennsylvania, 19140
CCOP - Metro-Minnesota
Saint Louis Park, Minnesota, 55416
St. Joseph's Hospital
Savannah, Georgia, 31419
David C. Pratt Cancer Center at St. John's Mercy
St Louis, Missouri, 63141
Canada3 sites
McGill Cancer Centre at McGill University
Montreal, Quebec, H2W 1S6
Ottawa Regional Cancer Centre at Ottawa Hospital - General Campus
Ottawa, Ontario, K1H 1C4
Regional Cancer Care at Thunder Bay Regional Health Sciences Centre
Thunder Bay, Ontario, P7B 6V4
About this study
Official title: An Open Label, Randomized, Controlled, Phase III, Multi-center, Clinical Trial Of PN401 With High Dose 5-Fluorouracil (5FU) Versus Gemcitabine For Treatment Of Patients With Advanced Pancreatic Cancer
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Giving the drugs in different combinations may kill more tumor cells. Chemoprotective drugs such as triacetyluridine may protect normal cells from the side effects of chemotherapy. It is not yet known which chemotherapy regimen is more effective in treating pancreatic cancer.
PURPOSE: Randomized phase III trial to compare the effectiveness of fluorouracil plus triacetyluridine with that of gemcitabine in treating patients who have locally advanced or metastatic pancreatic cancer that cannot be treated with surgery.
Read the detailed description
OBJECTIVES:
- Compare the survival of patients with unresectable locally advanced or metastatic pancreatic cancer treated with triacetyluridine and high-dose fluorouracil vs gemcitabine.
- Compare the time to tumor progression, overall response rate, and response duration in patients treated with these regimens.
- Compare the safety of these regimens in these patients.
OUTLINE: This is a randomized, open-label, multicenter study. Patients are stratified according to disease stage (II or III vs IV). Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients receive high-dose fluorouracil (5-FU) IV over 30 minutes once weekly on weeks 1-3 followed by 1 week of rest. After each dose of 5-FU, patients receive oral triacetyluridine every 8 hours for a total of 8 doses. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity.
- Arm II: Patients receive gemcitabine IV over 30 minutes once weekly on weeks 1-7 followed by 1 week of rest (course 1). Subsequent courses are given on weeks 1-3. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity.
Patients are followed for survival.
PROJECTED ACCRUAL: A total of 260 patients (130 per treatment arm) will be accrued for this study within 30 months.
- Being tested
- fluorouracil, gemcitabine hydrochloride, triacetyluridine
- Keywords
- drug/agent toxicity by tissue/organ, stage II pancreatic cancer, stage III pancreatic cancer, recurrent pancreatic cancer, adenocarcinoma of the pancreas, stage IV pancreatic cancer
- Medical subject headings
- Drug-Related Side Effects and Adverse Reactions, Pancreatic Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
fluorouracilDrug
Also called 5-FU
High dose 5-FU
Also called Gemzar
Normal dose to treat pancreatic cancer
triacetyluridineDrug
Also called 2',3',5'tri-O-acetyluridine
6 grams (12 tablets)
What is being measured
The primary outcome is the main question the study is designed to answer.
Open Label Randomized Phase 3 Multi-Center Trial of PN401 plus high dose 5-FU versus Gemcitabine in Advanced Pancreatic Cancer Patients
Measured: Disease progression
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Jan 2003 (estimated)
- Study startFeb 2001
- Primary completionFeb 2006
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Drug/Agent Toxicity by Tissue/OrganStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 250 participants (actual)
Sponsor and investigators
- Lead sponsor
- Wellstat Therapeutics
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Lenny Smith, MS, Study chair, Wellstat Therapeutics
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00024427
- Sponsor's protocol ID
- CDR0000068931
- Other IDs
- WELLSTAT-401.00.001, PRONEURON-401.00.001, UAB-0105, UAB-F010524008
- Status last verified
- May 2010
- First submitted
- 13 Sep 2001
- Last updated
- 28 Jun 2012
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 28 Jun 2012. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Open Label, Randomized, Controlled, Phase III, Multi-center, Clinical Trial Of PN401 With High Dose 5-Fluorouracil (5FU) Versus Gemcitabine For Treatment Of Patients With Advanced Pancreatic Cancer
- ClinicalTrials.gov ID
- NCT00024427
- Acronym / sponsor ID
- CDR0000068931
- Keywords
- drug/agent toxicity by tissue/organ, stage II pancreatic cancer, stage III pancreatic cancer, recurrent pancreatic cancer, adenocarcinoma of the pancreas, stage IV pancreatic cancer
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 250 participants (actual)
- Lead sponsor
- Wellstat TherapeuticsIndustry (pharma, biotech, devices)
- Study start
- Feb 2001
- Primary completion
- Feb 2006 (actual)
- First posted
- 27 Jan 2003 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Giving the drugs in different combinations may kill more tumor cells. Chemoprotective drugs such as triacetyluridine may protect normal cells from the side effects of chemotherapy. It is not yet known which chemotherapy regimen is more effective in treating pancreatic cancer.
PURPOSE: Randomized phase III trial to compare the effectiveness of fluorouracil plus triacetyluridine with that of gemcitabine in treating patients who have locally advanced or metastatic pancreatic cancer that cannot be treated with surgery.
Detailed description
OBJECTIVES:
- Compare the survival of patients with unresectable locally advanced or metastatic pancreatic cancer treated with triacetyluridine and high-dose fluorouracil vs gemcitabine.
- Compare the time to tumor progression, overall response rate, and response duration in patients treated with these regimens.
- Compare the safety of these regimens in these patients.
OUTLINE: This is a randomized, open-label, multicenter study. Patients are stratified according to disease stage (II or III vs IV). Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients receive high-dose fluorouracil (5-FU) IV over 30 minutes once weekly on weeks 1-3 followed by 1 week of rest. After each dose of 5-FU, patients receive oral triacetyluridine every 8 hours for a total of 8 doses. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity.
- Arm II: Patients receive gemcitabine IV over 30 minutes once weekly on weeks 1-7 followed by 1 week of rest (course 1). Subsequent courses are given on weeks 1-3. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity.
Patients are followed for survival.
PROJECTED ACCRUAL: A total of 260 patients (130 per treatment arm) will be accrued for this study within 30 months.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| fluorouracilAlso: 5-FUHigh dose 5-FU | Drug | – |
| gemcitabine hydrochlorideAlso: GemzarNormal dose to treat pancreatic cancer | Drug | – |
| triacetyluridineAlso: 2',3',5'tri-O-acetyluridine6 grams (12 tablets) | Drug | – |
Primary outcome
Open Label Randomized Phase 3 Multi-Center Trial of PN401 plus high dose 5-FU versus Gemcitabine in Advanced Pancreatic Cancer Patients
Time frame: Disease progression
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Jun 2012.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Lenny Smith, MS study chair
Wellstat Therapeutics
29 sites in 2 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing fluorouracil, gemcitabine hydrochloride and triacetyluridine in people with Drug/Agent Toxicity by Tissue/Organ and Pancreatic Cancer, run by Wellstat Therapeutics at 29 sites in 2 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 28 Jun 2012. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 29 sites in United States, Canada. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Open Label Randomized Phase 3 Multi-Center Trial of PN401 plus high dose 5-FU versus Gemcitabine in Advanced Pancreatic Cancer Patients (time frame: Disease progression). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Jun 2012.