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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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
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

Other trials in United States

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

Other trials in Canada

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

  • gemcitabine hydrochlorideDrug

    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.

  1. 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.

  1. First posted27 Jan 2003 (estimated)
  2. Study startFeb 2001
  3. Primary completionFeb 2006

Resources

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)
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

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.

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