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NCT00015886 · ClinicalTrials.gov registry record · Phase 2

Combination Chemotherapy in Treating Women With Breast Cancer That is Metastatic or Cannot be Treated With Surgery

A Phase 2 study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
Phase 2
Development phase
25
Enrollment target

NCT00015886: Completed Phase 2 study, sponsored by Wake Forest University Health Sciences.

NCT00015886 is a Phase 2 study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 25 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00015886, a Phase 2 study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
Phase 2
Development phase
25 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy in treating women who have breast cancer that is metastatic or cannot be treated with surgery.

Interventions

  • DRUG docetaxel
  • DRUG fluorouracil

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 1997-01
Est. Completion 2009-07
Phase Phase 2
Wake Forest University Health Sciences

1,140 total trials

What the finished NCT00015886 record still lists

NCT00015886 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (81% lower).

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

NCT00015886 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00015886 about?

NCT00015886 is a clinical study titled "Combination Chemotherapy in Treating Women With Breast Cancer That is Metastatic or Cannot be Treated With Surgery". RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy in treating women who have breast cancer tha...

What is the current status of trial NCT00015886?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 25 participants. The study started on 1997-01. Estimated completion is 2009-07.

What interventions are being tested in trial NCT00015886?

The interventions under investigation include: docetaxel (DRUG), fluorouracil (DRUG).

Who is sponsoring clinical trial NCT00015886?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00015886's enrollment target sits among peer trials

25 1719th of 2000 higher than 245 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 NCT00015886, the US trial registry maintained by the National Library of Medicine. NCT00015886 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.