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NCT00041106 · ClinicalTrials.gov registry record · Phase 2

Gefitinib Plus Combination Chemotherapy in Treating Patients With Locally Advanced or Metastatic Bladder Cancer

A Phase 2 study, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 2
Development phase
50
Enrollment target

NCT00041106: Completed Phase 2 study, sponsored by National Cancer Institute (NCI).

NCT00041106 is a Phase 2 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 50 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (62% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00041106, a Phase 2 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 2
Development phase
50 participants
Enrollment target

Study Summary

Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Biological therapies such as gefitinib may interfere with the growth of the tumor cells and slow the growth of the tumor. Combining chemotherapy with gefitinib may kill more tumor cells. Phase II trial to study the effectiveness of combining chemotherapy with gefitinib in treating patients who have metastatic transitional cell cancer of the urothelium

Primary Outcome

Exact 95% confidence intervals based on the binomial distribution will be computed.

Interventions

  • OTHER laboratory biomarker analysis
  • DRUG cisplatin
  • DRUG gemcitabine hydrochloride
  • DRUG gefitinib

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2002-05
Phase Phase 2
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00041106 record still lists

NCT00041106 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (62% lower).

The record links to 0 conditions, and to 4 interventions - of which laboratory biomarker analysis is the first listed.

NCT00041106 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00041106 about?

NCT00041106 is a clinical study titled "Gefitinib Plus Combination Chemotherapy in Treating Patients With Locally Advanced or Metastatic Bladder Cancer". Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Biological therapies such as gefitinib may interfere with the growth of the tumor cells and slow the growth of the tumor. Combining chemotherapy with gefitinib may kill more tumor cells. Phas...

What is the current status of trial NCT00041106?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 50 participants. The study started on 2002-05.

What interventions are being tested in trial NCT00041106?

The interventions under investigation include: laboratory biomarker analysis (OTHER), cisplatin (DRUG), gemcitabine hydrochloride (DRUG), gefitinib (DRUG).

Who is sponsoring clinical trial NCT00041106?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00041106's enrollment target sits among peer trials

50 1195th of 2000 higher than 740 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 NCT00041106, the US trial registry maintained by the National Library of Medicine. NCT00041106 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.