Clinical Trials Directory

Trials / Terminated

TerminatedNCT01229111

Cediranib Maleate and Combination Chemotherapy in Treating Patients With Advanced Biliary Cancers

A Phase 2 Study of AZD2171 (Cediranib) With Modified FOLFOX6 in Patients With Advanced Biliary Cancers

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
14 (actual)
Sponsor
National Cancer Institute (NCI) · NIH
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This phase II trial is studying how well giving cediranib maleate together with combination chemotherapy works in treating patients with advanced biliary cancers. Cediranib maleate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth or by blocking blood flow to the tumor. Drugs used in chemotherapy, such as oxaliplatin, leucovorin calcium, and fluorouracil, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving cediranib maleate together with combination chemotherapy may kill more tumor cells.

Detailed description

PRIMARY OBJECTIVES: I. To determine the response rate to AZD2171 (cediranib maleate) and modified folinic acid-fluorouracil-oxaliplatin-6 regimen (FOLFOX 6) in subjects with advanced biliary cancers. SECONDARY OBJECTIVES: I. To determine overall assessment of toxicity of AZD2171 and modified FOLFOX6. II. To determine the progression-free survival of subjects with advanced biliary cancers treated with AZD2171 and modified FOLFOX6. III. To determine overall survival of subjects with advanced biliary cancers treated with AZD2171 and modified FOLFOX6. OUTLINE: Patients receive cediranib maleate orally (PO) once daily (QD) on days 1-14 and modified FOLFOX6 comprising oxaliplatin intravenously (IV) over 2 hours, leucovorin calcium IV over 2 hours, and fluorouracil IV over 46 hours on day 1. Courses repeat every 14 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up every 3 months for 1 year, every 6 months for 2 years, and then annually thereafter.

Conditions

Interventions

TypeNameDescription
DRUGcediranib maleateGiven PO
DRUGoxaliplatinGiven IV
DRUGleucovorin calciumGiven IV
DRUGfluorouracilGiven IV

Timeline

Start date
2010-10-01
Primary completion
2014-03-01
Completion
2014-03-01
First posted
2010-10-27
Last updated
2017-03-29
Results posted
2017-03-29

Locations

7 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01229111. Inclusion in this directory is not an endorsement.