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NCT01705106 · ClinicalTrials.gov registry record · Phase 1

Capecitabine and Celecoxib in Patients With Solid Cancers That Have Been Previously Treated With Standard Therapies

A Phase 1 study, sponsored by University of Chicago.

Terminated
Registry status
Phase 1
Development phase
21
Enrollment target

NCT01705106 is a Phase 1 study that was terminated before completion, run by University of Chicago. The registered enrollment target is 21 participants.

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The verdict

NCT01705106, a Phase 1 study, was terminated before completion, sponsored by University of Chicago.

TERMINATED
Registry status
Phase 1
Development phase
21 participants
Enrollment target

Study Summary

This clinical trial studies capecitabine and celecoxib in treating patients with solid malignancies that are metastatic or cannot be removed by surgery. Drugs used in chemotherapy, such as capecitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Celecoxib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving capecitabine and celecoxib together may be an effective treatment for solid malignancies.

Interventions

  • OTHER laboratory biomarker analysis
  • DRUG capecitabine
  • OTHER pharmacological study
  • OTHER pharmacogenomic studies
  • DRUG celecoxib

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2012-08-29
Est. Completion 2016-02-10
Phase Phase 1

Sponsor

University of Chicago

796 total trials

What the Registry Record Tells You About NCT01705106

The ClinicalTrials.gov registry entry for NCT01705106 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 21 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Chicago, which has 796 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 5 interventions - of which laboratory biomarker analysis is the first listed.

NCT01705106 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01705106 about?

NCT01705106 is a clinical study titled "Capecitabine and Celecoxib in Patients With Solid Cancers That Have Been Previously Treated With Standard Therapies". This clinical trial studies capecitabine and celecoxib in treating patients with solid malignancies that are metastatic or cannot be removed by surgery. Drugs used in chemotherapy, such as capecitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopp...

What is the current status of trial NCT01705106?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 21 participants. The study started on 2012-08-29. Estimated completion is 2016-02-10.

What interventions are being tested in trial NCT01705106?

The interventions under investigation include: laboratory biomarker analysis (OTHER), capecitabine (DRUG), pharmacological study (OTHER), pharmacogenomic studies (OTHER), celecoxib (DRUG).

Who is sponsoring clinical trial NCT01705106?

This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.