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NCT00038168 · ClinicalTrials.gov registry record · Phase 1

Intravenous Estramustine With Taxol in Hormone Refractory Prostate Adenocarcinoma

A Phase 1 study, sponsored by M.D. Anderson Cancer Center.

Completed
Registry status
Phase 1
Development phase
14
Enrollment target

NCT00038168: Completed Phase 1 study, sponsored by M.D. Anderson Cancer Center.

NCT00038168 is a Phase 1 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 14 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00038168, a Phase 1 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
14 participants
Enrollment target

Study Summary

Phase I: The goal of this clinical research study is to find the highest dose of estramustine phosphate administered intravenously in combination with a fixed dose of Taxol (paclitaxel) that can be given safely to participants with prostate cancer who have failed to further benefit from hormone treatment. Phase II: The goal of this clinical research study is to find out if the combination of the drugs estramustine phosphate and paclitaxel will shrink or control prostate cancer that has not responded to hormone treatment. A second goal is to find out if the side effects of these drugs can be reversed. The safety of these drugs will also be studied.

Interventions

  • DRUG Taxol
  • DRUG Estramustine

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2000-06
Est. Completion 2003-01
Phase Phase 1
M.D. Anderson Cancer Center

2,692 total trials

What the finished NCT00038168 record still lists

NCT00038168 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (77% lower).

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

NCT00038168 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00038168 about?

NCT00038168 is a clinical study titled "Intravenous Estramustine With Taxol in Hormone Refractory Prostate Adenocarcinoma". Phase I: The goal of this clinical research study is to find the highest dose of estramustine phosphate administered intravenously in combination with a fixed dose of Taxol (paclitaxel) that can be given safely to participants with prostate cancer who have failed to further benefit from hormone trea...

What is the current status of trial NCT00038168?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 14 participants. The study started on 2000-06. Estimated completion is 2003-01.

What interventions are being tested in trial NCT00038168?

The interventions under investigation include: Taxol (DRUG), Estramustine (DRUG).

Who is sponsoring clinical trial NCT00038168?

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 NCT00038168's enrollment target sits among peer trials

14 1844th of 2000 higher than 154 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00038168, the US trial registry maintained by the National Library of Medicine. NCT00038168 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.