Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00022633 · ClinicalTrials.gov registry record · Phase 2

S0028, Gemcitabine and Paclitaxel in Treating Patients With Advanced or Recurrent Cancer of the Urinary Tract

A Phase 2 study, sponsored by SWOG Cancer Research Network.

Terminated
Registry status
Phase 2
Development phase
65
Enrollment target

NCT00022633: Clinical Trial Phase 2 study, sponsored by SWOG Cancer Research Network.

NCT00022633 is a Phase 2 study that was terminated before completion, run by SWOG Cancer Research Network. The registered enrollment target is 65 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (51% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00022633, a Phase 2 study, was terminated before completion, sponsored by SWOG Cancer Research Network.

TERMINATED
Registry status
Phase 2
Development phase
65 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. Giving more than one drug may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of combining gemcitabine and paclitaxel in treating patients who have advanced or recurrent cancer of the urinary tract.

Primary Outcome

Sixty patients aged 70 years and older were to be accrued to the study. The feasibility of accrual was determined that accrual of 3 patients per month in the age 70 and older range would allow for an expeditiously conducted phase II trial. If, after a 3 month start-up period, 3 or more patients aged 70 years and older were accrued per month for the duration of the trial, it was deemed reasonable to consider further trials in this elderly population.

Interventions

  • DRUG paclitaxel
  • DRUG gemcitabine hydrochloride

Trial Details

FieldValue
Enrollment Target 65 participants
Start Date 2001-07
Est. Completion 2011-07
Phase Phase 2
SWOG Cancer Research Network

270 total trials

Why NCT00022633 stopped before completion

NCT00022633 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 65 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (51% lower).

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

NCT00022633 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00022633 about?

NCT00022633 is a clinical study titled "S0028, Gemcitabine and Paclitaxel in Treating Patients With Advanced or Recurrent Cancer of the Urinary Tract". RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Giving more than one drug may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of combining gemcitabine and paclitaxel in treating patients who have advan...

What is the current status of trial NCT00022633?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 65 participants. The study started on 2001-07. Estimated completion is 2011-07.

What interventions are being tested in trial NCT00022633?

The interventions under investigation include: paclitaxel (DRUG), gemcitabine hydrochloride (DRUG).

Who is sponsoring clinical trial NCT00022633?

This trial is sponsored by SWOG Cancer Research Network, which has 270 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00022633's enrollment target sits among peer trials

65 987th of 2000 higher than 1,005 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03366116 · 65 participants · Phase 1

    5-aza-4'-Thio-2'-Deoxycytidine (Aza-TdC) in People With Advanced Solid Tumors

  • NCT03603730 · 65 participants · NA

    Vagal Nerve Stimulation for Functional Dyspepsia and Gastroparesis

  • NCT03796559 · 65 participants · NA

    Magseed Enabled Long-Term Localization of Axillary Lymph Nodes

  • NCT03993106 · 65 participants · Phase 2

    A Study of sEphB4-HSA in Kaposi Sarcoma

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00022633, the US trial registry maintained by the National Library of Medicine. NCT00022633 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.