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NCT00084825 · ClinicalTrials.gov registry record · Phase 2

Docetaxel and Imatinib Mesylate in Treating Patients With Androgen-Independent Prostate Cancer and Bone Metastases That Progressed on the Docetaxel and Placebo Group of MDA-ID-030008

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

Completed
Registry status
Phase 2
Development phase
23
Enrollment target

NCT00084825: Completed Phase 2 study, sponsored by M.D. Anderson Cancer Center.

NCT00084825 is a Phase 2 study that has completed, run by M.D. Anderson Cancer Center. 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

NCT00084825, a Phase 2 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
23 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. Giving docetaxel with imatinib mesylate may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving docetaxel with imatinib mesylate works in treating patients with androgen-independent prostate cancer and bone metastases that progressed while receiving docetaxel and a placebo on clinical trial MDA-ID-030008.

Interventions

  • DRUG Docetaxel
  • DRUG Imatinib mesylate

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2003-05
Est. Completion 2008-06
Phase Phase 2
M.D. Anderson Cancer Center

2,692 total trials

What the finished NCT00084825 record still lists

NCT00084825 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 2 interventions - of which Docetaxel is the first listed.

NCT00084825 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00084825 about?

NCT00084825 is a clinical study titled "Docetaxel and Imatinib Mesylate in Treating Patients With Androgen-Independent Prostate Cancer and Bone Metastases That Progressed on the Docetaxel and Placebo Group of MDA-ID-030008". 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. Giving docetaxel with imatinib mesylate may kill more...

What is the current status of trial NCT00084825?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 23 participants. The study started on 2003-05. Estimated completion is 2008-06.

What interventions are being tested in trial NCT00084825?

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

Who is sponsoring clinical trial NCT00084825?

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 NCT00084825'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 NCT00084825, the US trial registry maintained by the National Library of Medicine. NCT00084825 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.