CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 44 enrolled
Drug / intervention
Capecitabine +1 moredrug
Likely dose
Capecitabine 1500 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00338988
NCT00338988Phase 2Completed

A Phase II Study of Oxaliplatin and Capecitabine in Patients With Unresectable Cholangiocarcinoma, Including Carcinoma of the Gallbladder and Biliary Tract

M.D. Anderson Cancer Center·interventional·Posted Jun 20, 2006·Updated Aug 1, 2012

In Brief

A Phase 2 clinical trial evaluating Capecitabine and Oxaliplatin for Cancer of the Gallbladder and Cancer of the Biliary Tract. Completed, enrolled 44 participants across 1 site.

Detailed Summary

This is a Phase II trial of the combination of oxaliplatin (Eloxatin) and capecitabine (Xeloda), known as XELOX, in participants with unresectable or recurrent cholangiocarcinoma, including carcinoma of the gallbladder or biliary tract, both intrahepatic and extrahepatic. Participants may be either previously untreated or treated with chemotherapy. Participants will accrue to two strata based on pre-treatment status; separate response rates and statistical operating characteristics will be applied to each stratum. The primary objective is to determine the objective response rate (complete plus partial) of XELOX in this population. Secondary objectives include determining toxicity, stable disease rates, and median and overall survival of participants treated with this combination.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsSanofi-Synthelabo

Timeline

Phase 2CompletedFinished
2003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJun 20, 2006
Enrollment StartAug 1, 2003
Primary CompletionMay 1, 2009
TodayJul 2, 2026
Enrollment to primary: 5.8 yearsPosted 20.0 years ago

Interventions

Capecitabinedrug

1500 mg/m\^2 PO twice daily x 14 days.

Oxaliplatindrug

130 mg/m\^2 IV over 2 hours on day 1 of cycle.