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NCT00262951 · ClinicalTrials.gov registry record · Phase 2

Chemoradiation in Locally Advanced Pancreatic Cancer

A Phase 2 study, sponsored by Masonic Cancer Center, University of Minnesota.

Terminated
Registry status
Phase 2
Development phase
23
Enrollment target

NCT00262951: Clinical Trial Phase 2 study, sponsored by Masonic Cancer Center, University of Minnesota.

NCT00262951 is a Phase 2 study that was terminated before completion, run by Masonic Cancer Center, University of Minnesota. The registered enrollment target is 23 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00262951, a Phase 2 study, was terminated before completion, sponsored by Masonic Cancer Center, University of Minnesota.

TERMINATED
Registry status
Phase 2
Development phase
23 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy, such as fluorouracil and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. Radiation therapy uses high-energy x-rays to kill tumor cells. Interferon alfa may interfere with the growth of tumor cells. Giving combination chemotherapy and radiation therapy together with interferon alfa before surgery may shrink the tumor so it can be removed. Giving chemotherapy after surgery may kill any tumor cells that remain after surgery. PURPOSE: This phase II trial is studying how well giving combination chemotherapy and radiation therapy together with interferon alfa works in treating patients with locally advanced pancreatic cancer that cannot be removed by surgery.

Primary Outcome

Tumor response is measured in terms of resectability, as measured by CT scan at 2 weeks after completion of each course. A CT scan of the chest abdomen and pelvis will be performed in order to evaluate for the presence of metastatic disease. If no metastatic disease, emphasis will be paid to the local tumor. Evaluation of the growth/regression of the tumor will be made as it relates to resectability. If potential for resection then surgery will be recommended. This protocol will be followed afte

Interventions

  • DRUG cisplatin
  • DRUG fluorouracil
  • RADIATION radiation therapy
  • BIOLOGICAL recombinant interferon alfa
  • PROCEDURE Resection of tumor

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2005-01
Est. Completion 2011-08
Phase Phase 2

Why NCT00262951 stopped before completion

NCT00262951 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (83% lower).

The record links to 0 conditions, and to 5 interventions - of which cisplatin is the first listed.

NCT00262951 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00262951 about?

NCT00262951 is a clinical study titled "Chemoradiation in Locally Advanced Pancreatic Cancer". RATIONALE: Drugs used in chemotherapy, such as fluorouracil and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. Radiation therapy uses h...

What is the current status of trial NCT00262951?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 23 participants. The study started on 2005-01. Estimated completion is 2011-08.

What interventions are being tested in trial NCT00262951?

The interventions under investigation include: cisplatin (DRUG), fluorouracil (DRUG), radiation therapy (RADIATION), recombinant interferon alfa (BIOLOGICAL), Resection of tumor (PROCEDURE).

Who is sponsoring clinical trial NCT00262951?

This trial is sponsored by Masonic Cancer Center, University of Minnesota, which has 249 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00262951's enrollment target sits among peer trials

23 1784th of 2000 higher than 211 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00262951, the US trial registry maintained by the National Library of Medicine. NCT00262951 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.