CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 56 enrolled
Drug / intervention
erlotinib hydrochloride +1 moredrug
Likely dose
erlotinib hydrochloride 150 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/NCT00356889
NCT00356889Phase 2Completed

A Phase II Trial of Bevacizumab and Erlotinib in Patients With Advanced Biliary Tumors

National Cancer Institute (NCI)·interventional·Posted Jul 27, 2006·Updated May 28, 2014

In Brief

A Phase 2 clinical trial evaluating erlotinib hydrochloride and bevacizumab for Cholangiocarcinoma of the Extrahepatic Bile Duct and 6 related conditions. Completed, enrolled 56 participants across 1 site.

Detailed Summary

This phase II trial is studying how well giving bevacizumab together with erlotinib hydrochloride works in treating patients with metastatic or unresectable biliary tumors. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Erlotinib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Bevacizumab and erlotinib hydrochloride may also stop the growth of tumor cells by blocking blood flow to the tumor. Giving bevacizumab together with erlotinib hydrochloride may kill more tumor cells.

Study Details

Timeline

Phase 2CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJul 27, 2006
Enrollment StartMay 1, 2006
Primary CompletionOct 1, 2008
Study CompletionJun 1, 2010
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 19.9 years ago

Interventions

erlotinib hydrochloridedrug

Given orally, 150 mg, once daily.

bevacizumabbiological

Given IV, 5mg/kg on days 1 and 15 every cycle