Clinical Trials Directory

Trials / Terminated

TerminatedNCT00683787

Docetaxel With or Without Vandetanib in Treating Patients With Metastatic Stomach Cancer or Gastroesophageal Junction Cancer

Multicenter Randomized Phase II Trial of Docetaxel With/Without VANDETANIB for Advanced Gastroesophageal Cancer

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
8 (actual)
Sponsor
Roswell Park Cancer Institute · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Vandetanib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. It is not yet known whether docetaxel is more effective when given together with or without vandetanib. PURPOSE: This randomized phase II trial is studying docetaxel to see how well it works compared with docetaxel given together with vandetanib in treating patients with metastatic stomach cancer or gastroesophageal junction cancer.

Detailed description

OBJECTIVES: Primary * To test the hypothesis that the addition of a targeted agent, such as vandetanib, to standard chemotherapy with docetaxel will result in incremental responses in patients with metastatic gastric or gastroesophageal junction cancer. Secondary * To assess progression-free survival and overall survival of patients treated with this regimen. * To study the toxicity profile of this regimen in these patients. OUTLINE: This is a multicenter study. Patients are stratified according to clinical site. Patients are randomized to 1 of 3 treatment arms. * Arm I: Patients receive docetaxel IV once every 3 weeks. * Arm II: Patients receive docetaxel IV as in arm I and oral vandetanib (100 mg) once daily. * Arm III: Patients receive docetaxel IV as in arm I and oral vandetanib (300 mg) once daily. In all arms, courses repeat every 3 weeks in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed every 2 months for 5 years.

Conditions

Interventions

TypeNameDescription
DRUGdocetaxelGiven IV once every 3 weeks
DRUGvandetanibOral vandetanib once daily

Timeline

Start date
2008-05-01
Primary completion
2009-04-01
Completion
2011-03-01
First posted
2008-05-23
Last updated
2015-01-08
Results posted
2015-01-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00683787. Inclusion in this directory is not an endorsement.