Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00054470

Tipifarnib Plus Trastuzumab in Treating Patients With Metastatic Breast Cancer

A Phase II Evaluation Of The Efficacy And Safety Of R115777 (NSC702818) A Non-Peptidomimetic Farnesyl Transferase Inhibitor, And Trastuzumab In Patients With Advanced Breast Cancer

Status
Withdrawn
Phase
Phase 2
Study type
Interventional
Enrollment
0 (actual)
Sponsor
The University of Texas Health Science Center at San Antonio · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Tipifarnib may stop the growth of tumor cells by blocking the enzymes necessary for tumor cell growth. Monoclonal antibodies such as trastuzumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Combining tipifarnib with trastuzumab may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of combining tipifarnib with trastuzumab in treating patients who have metastatic breast cancer.

Detailed description

OBJECTIVES: * Determine the antitumor activity of tipifarnib and trastuzumab (Herceptin) in patients with metastatic breast cancer. * Determine the safety and tolerability of this regimen in these patients. OUTLINE: This is an open-label, multicenter study. Patients receive oral tipifarnib twice daily on days 1-21 and trastuzumab (Herceptin) IV over 30-90 minutes on day 1. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity. Patients are followed every 2 months. PROJECTED ACCRUAL: A total of 18-40 patients will be accrued for this study within 9-20 months.

Conditions

Interventions

TypeNameDescription
BIOLOGICALtrastuzumab
DRUGtipifarnib

Timeline

Start date
2002-12-01
Primary completion
2003-01-01
Completion
2003-01-01
First posted
2003-02-06
Last updated
2012-06-29

Source: ClinicalTrials.gov record NCT00054470. Inclusion in this directory is not an endorsement.