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COMPLETED Phase 2

Docetaxel and Capecitabine in Treating Patients With Metastatic Cancer of the Stomach or Gastroesophageal Junction

NCT00054457 · View on ClinicalTrials.gov ↗

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 of the effectiveness of combining docetaxel with capecitabine in treating patients who have metastatic cancer of the stomach or gastroesophageal junction.

Interventions

  • DRUG docetaxel
  • DRUG capecitabine

Study Locations (20)

Kansas

  • Cancer Center of Kansas, PA - Chanute — Chanute
  • Cancer Center of Kansas, PA - Dodge City — Dodge City
  • Cancer Center of Kansas, PA - El Dorado — El Dorado
  • Cancer Center of Kansas, PA - Kingman — Kingman
  • Southwest Medical Center — Liberal
  • Cancer Center of Kansas, PA - Newton — Newton
  • Cancer Center of Kansas, PA - Parsons — Parsons
  • Cancer Center of Kansas, PA - Pratt — Pratt
  • Cancer Center of Kansas, PA - Salina — Salina
  • Cancer Center of Kansas, PA - Wellington — Wellington
  • Associates in Womens Health, PA - North Review — Wichita
  • Cancer Center of Kansas, PA - Medical Arts Tower — Wichita
  • Cancer Center of Kansas, PA - Wichita — Wichita
  • CCOP - Wichita — Wichita
  • Via Christi Cancer Center at Via Christi Regional Medical Center — Wichita
  • Cancer Center of Kansas, PA - Winfield — Winfield

Minnesota

  • Fairview Ridges Hospital — Burnsville
  • Mercy and Unity Cancer Center at Mercy Hospital — Coon Rapids
  • Fairview Southdale Hospital — Edina
  • Mercy and Unity Cancer Center at Unity Hospital — Fridley

Trial Details

FieldValue
Enrollment Target 46 participants
Start Date 2003-09
Est. Completion 2008-02
Phase Phase 2

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00054457

The ClinicalTrials.gov registry entry for NCT00054457 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 46 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alliance for Clinical Trials in Oncology, which has 147 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Gastric Cancer appearing as the primary indexed condition, and to 2 interventions — of which docetaxel is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00054457 reports 20 study locations spanning 2 distinct geographic areas — top geographies include Kansas, Minnesota. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00054457 about?

NCT00054457 is a clinical study titled "Docetaxel and Capecitabine in Treating Patients With Metastatic Cancer of the Stomach or Gastroesophageal Junction". 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 of the effectiveness of combining docetaxel with capecitabine in treating patients who hav...

What is the current status of trial NCT00054457?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 46 participants. The study started on 2003-09. Estimated completion is 2008-02.

What conditions does trial NCT00054457 study?

This clinical trial studies the following conditions: Gastric Cancer, Esophageal Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00054457?

The interventions under investigation include: docetaxel (DRUG), capecitabine (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00054457?

This trial is sponsored by Alliance for Clinical Trials in Oncology, which has 147 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00054457 being conducted?

This trial has 20 study locations across Kansas, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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