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NCT00357500 · ClinicalTrials.gov registry record · Phase 2

Etoposide, Cyclophosphamide, Thalidomide, Celecoxib, and Fenofibrate in Relapsed or Progressive Cancer

A Phase 2 study, sponsored by Dana-Farber Cancer Institute.

Completed
Registry status
Phase 2
Development phase
101
Enrollment target

NCT00357500: Completed Phase 2 study, sponsored by Dana-Farber Cancer Institute.

NCT00357500 is a Phase 2 study that has completed, run by Dana-Farber Cancer Institute. The registered enrollment target is 101 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (24% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00357500, a Phase 2 study, has completed, sponsored by Dana-Farber Cancer Institute.

COMPLETED
Registry status
Phase 2
Development phase
101 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy, such as etoposide and cyclophosphamide, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Thalidomide, celecoxib, and fenofibrate may stop the growth of cancer cells by blocking blood flow to the cancer. Celecoxib also may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving combination chemotherapy together with thalidomide, celecoxib, and fenofibrate may kill more cancer cells. PURPOSE: This phase II trial is studying how well giving etoposide and cyclophosphamide together with thalidomide, celecoxib, and fenofibrate works in treating young patients with relapsed or progressive cancer.

Primary Outcome

Proportion of patients alive at 27 weeks without progressive disease (PD) and having tolerated therapy. As appropriate for tumor type and location, gadolinium-enhanced MRI and other imaging modalites were used to assess response. Progressive disease was defined as \>/=25% increase in product of diameters, development of new areas of disease, or disease-attributable clinical deterioration or death, progressive disease. For patients with leukemia PD was defined as \>/=25% or \>/=5,000 cells/mm3 in

Interventions

  • DRUG cyclophosphamide
  • DRUG etoposide
  • DRUG fenofibrate
  • DRUG thalidomide
  • DRUG celecoxib

Trial Details

FieldValue
Enrollment Target 101 participants
Start Date 2005-01
Est. Completion 2013-12
Phase Phase 2
Dana-Farber Cancer Institute

781 total trials

What the finished NCT00357500 record still lists

NCT00357500 is an interventional study that assigns participants to a tested intervention. The registered 101 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (24% lower).

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

NCT00357500 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00357500 about?

NCT00357500 is a clinical study titled "Etoposide, Cyclophosphamide, Thalidomide, Celecoxib, and Fenofibrate in Relapsed or Progressive Cancer". RATIONALE: Drugs used in chemotherapy, such as etoposide and cyclophosphamide, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Thalidomide, celecoxib, and fenofibrate may stop the growth of cancer cells by blocking blood flow ...

What is the current status of trial NCT00357500?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 101 participants. The study started on 2005-01. Estimated completion is 2013-12.

What interventions are being tested in trial NCT00357500?

The interventions under investigation include: cyclophosphamide (DRUG), etoposide (DRUG), fenofibrate (DRUG), thalidomide (DRUG), celecoxib (DRUG).

Who is sponsoring clinical trial NCT00357500?

This trial is sponsored by Dana-Farber Cancer Institute, which has 781 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00357500's enrollment target sits among peer trials

101 672nd of 2000 higher than 1,329 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 NCT00357500, the US trial registry maintained by the National Library of Medicine. NCT00357500 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.