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Completed Phase 2 Interventional Results available

Oxaliplatin and Capecitabine in the Treatment of Relapsed/Refractory Carcinoma of Unknown Primary Site

ClinicalTrials.gov ID: NCT00193609

Public ClinicalTrials.gov record NCT00193609. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 2:32 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase II Trial of Oxaliplatin and Capecitabine in the Treatment of Patients With Relapsed/Refractory Carcinoma of Unknown Primary Site

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

In this phase II trial, we will evaluate the feasibility and efficacy of the oxaliplatin/capecitabine combination in patients who have had one previous chemotherapy regimen for the treatment of carcinoma of unknown primary site. Patients who are relapsed after a previous response to treatment will be eligible, as well as those who were refractory to first-line therapy.

Study identification

NCT ID
NCT00193609
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
48 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2004 (Type not available)
Primary completion
Apr 2008 (Actual)
Completion
Jan 2009 (Actual)
Last update posted
Nov 11, 2013

2004 – 2009

United States locations

U.S. sites
10
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
Integrated Community Oncology Network Jacksonville Florida 32256 —
AP&S Oncology & Hematology Northside Terre Haute Indiana 47804 —
Greenview Regional Hospital Bowling Green Kentucky 42104 —
Consultants in Blood Disorders and Cancer Louisville Kentucky 40207 —
Baton Rouge General Medical Center Baton Rouge Louisiana 70806 —
Oncology Hematology Care Cincinnati Ohio 45242 —
Reading Hospital Regional Cancer Center West Reading Pennsylvania 19612 —
Spartanburg Regional Medical Center Spartanburg South Carolina 29303 —
Chattanooga Oncology Hematology Associates Chattanooga Tennessee 37404 —
Tennessee Oncology, PLLC Nashville Tennessee 37023 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00193609, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 11, 2013 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00193609 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →