Clinical Trials Directory

Trials / Completed

CompletedNCT00003041

Pyrazoloacridine in Treating Women With Refractory Metastatic Breast Cancer

Phase II Evaluation of Pyrazoloacridine (NSC #366140) in Patients With Metastatic Breast Cancer

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
Sponsor
Ohio State University Comprehensive Cancer Center · Academic / Other
Sex
Female
Age
16 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase II trial to study the effectiveness of pyrazoloacridine in treating women who have refractory metastatic breast cancer.

Detailed description

OBJECTIVES: I. Determine the efficacy of pyrazoloacridine in patients with refractory breast cancer. II. Determine the toxic effects of pyrazoloacridine in these patients. OUTLINE: Patients receive pyrazoloacridine IV over 3 hours. Treatment repeats every 21 days for 2-8 courses in the absence of disease progression or unacceptable toxicity. PROJECTED ACCRUAL: A total of 12-35 patients will be accrued for this study within 1 year.

Conditions

Interventions

TypeNameDescription
DRUGpyrazoloacridine

Timeline

Start date
1997-07-01
Completion
2002-01-01
First posted
2004-04-23
Last updated
2013-01-31

Locations

5 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00003041. Inclusion in this directory is not an endorsement.

Pyrazoloacridine in Treating Women With Refractory Metastatic Breast Cancer (NCT00003041) · Clinical Trials Directory