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NCT04039867 · ClinicalTrials.gov registry record · Phase 2

Evaluation of Oxaliplatin and Gemcitabine in Patients With Metastatic Bladder Cancer

A Phase 2 study, sponsored by University of California, Irvine.

Terminated
Registry status
Phase 2
Development phase
17
Enrollment target

NCT04039867: Clinical Trial Phase 2 study, sponsored by University of California, Irvine.

NCT04039867 is a Phase 2 study that was terminated before completion, run by University of California, Irvine. The registered enrollment target is 17 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04039867, a Phase 2 study, was terminated before completion, sponsored by University of California, Irvine.

TERMINATED
Registry status
Phase 2
Development phase
17 participants
Enrollment target

Study Summary

This phase II trial evaluated the impact of Oxaliplatin and Gemcitabine in patients with recurrent or advanced transitional cell carcinoma of the bladder. The combination of Oxaliplatin and Gemcitabine is considered investigational and this study will help in determining if their activity and toxicity profiles are comparable or better than the standard regimens.

Primary Outcome

To evaluate the tolerability of administering Oxaliplatin in combination with gemcitabine in patients with recurrent or advanced TCC bladder. Toxicity and adverse events are based on the CTCAE (NCI Common Terminology Criteria for Adverse Events) Version 3.0.

Interventions

  • DRUG Oxaliplatin with Gemcitabine

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2005-01-20
Est. Completion 2011-10-06
Phase Phase 2
University of California, Irvine

368 total trials

Why NCT04039867 stopped before completion

NCT04039867 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (87% lower).

The record links to 0 conditions, and to 1 intervention - of which Oxaliplatin with Gemcitabine is the first listed.

NCT04039867 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04039867 about?

NCT04039867 is a clinical study titled "Evaluation of Oxaliplatin and Gemcitabine in Patients With Metastatic Bladder Cancer". This phase II trial evaluated the impact of Oxaliplatin and Gemcitabine in patients with recurrent or advanced transitional cell carcinoma of the bladder. The combination of Oxaliplatin and Gemcitabine is considered investigational and this study will help in determining if their activity and toxici...

What is the current status of trial NCT04039867?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 17 participants. The study started on 2005-01-20. Estimated completion is 2011-10-06.

What interventions are being tested in trial NCT04039867?

The interventions under investigation include: Oxaliplatin with Gemcitabine (DRUG).

Who is sponsoring clinical trial NCT04039867?

This trial is sponsored by University of California, Irvine, which has 368 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04039867's enrollment target sits among peer trials

17 1903rd of 2000 higher than 93 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 NCT04039867, the US trial registry maintained by the National Library of Medicine. NCT04039867 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.