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NCT00080678 · ClinicalTrials.gov registry record · Phase 2

Docetaxel With or Without Imatinib Mesylate in Treating Patients With Androgen-Independent Prostate Cancer and Bone Metastases

A Phase 2 study, sponsored by M.D. Anderson Cancer Center.

Completed
Registry status
Phase 2
Development phase
116
Enrollment target

NCT00080678: Completed Phase 2 study, sponsored by M.D. Anderson Cancer Center.

NCT00080678 is a Phase 2 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 116 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (13% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00080678, a Phase 2 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
116 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy, such as docetaxel, work in different ways to stop tumor cells from dividing so they stop growing or die. Imatinib mesylate may stop the growth of tumor cells by blocking the enzymes necessary for their growth. Combining docetaxel with imatinib mesylate may be effective treatment for androgen-independent prostate cancer and bone metastases. PURPOSE: This randomized phase II trial is studying docetaxel and imatinib mesylate to see how well they work compared to docetaxel alone in treating patients with androgen-independent prostate cancer and bone metastases.

Interventions

  • DRUG Docetaxel
  • DRUG Imatinib Mesylate

Trial Details

FieldValue
Enrollment Target 116 participants
Start Date 2003-05
Est. Completion 2008-03
Phase Phase 2
M.D. Anderson Cancer Center

2,692 total trials

What the finished NCT00080678 record still lists

NCT00080678 is an interventional study that assigns participants to a tested intervention. The registered 116 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 (13% lower).

The record links to 0 conditions, and to 2 interventions - of which Docetaxel is the first listed.

NCT00080678 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00080678 about?

NCT00080678 is a clinical study titled "Docetaxel With or Without Imatinib Mesylate in Treating Patients With Androgen-Independent Prostate Cancer and Bone Metastases". RATIONALE: Drugs used in chemotherapy, such as docetaxel, work in different ways to stop tumor cells from dividing so they stop growing or die. Imatinib mesylate may stop the growth of tumor cells by blocking the enzymes necessary for their growth. Combining docetaxel with imatinib mesylate may be e...

What is the current status of trial NCT00080678?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 116 participants. The study started on 2003-05. Estimated completion is 2008-03.

What interventions are being tested in trial NCT00080678?

The interventions under investigation include: Docetaxel (DRUG), Imatinib Mesylate (DRUG).

Who is sponsoring clinical trial NCT00080678?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00080678's enrollment target sits among peer trials

116 623rd of 2000 higher than 1,375 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 NCT00080678, the US trial registry maintained by the National Library of Medicine. NCT00080678 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.