Clinical Trials Directory

Trials / Completed

CompletedNCT00003768

Combretastatin A4 Phosphate in Treating Patients With Advanced Solid Tumors

A Phase I Pharmacokinetic Study of Single Dose Intravenous CA4P in Patients With Advanced Cancer

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
25 (actual)
Sponsor
Case Comprehensive Cancer Center · Academic / Other
Sex
All
Age
18 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 I trial to study the effectiveness of combretastatin A4 phosphate in treating patients who have advanced solid tumors that have not responded to previous therapy.

Detailed description

OBJECTIVES: I. Determine the maximum tolerated dose of combretastatin A4 phosphate when administered at single doses every 21 days in patients with advanced solid tumors. II. Determine both the toxicity and dose limiting toxicity of this regimen in these patients. III. Determine the plasma and urine pharmacokinetics of combretastatin A4 and combretastatin A4 phosphate. IV. Gather preliminary data regarding possible antitumor effects in those patients with measurable disease. OUTLINE: This is an open label, dose escalation study. Patients receive combretastatin A4 phosphate IV over 10-60 minutes. Treatment repeats every 3 weeks in the absence of unacceptable toxicity or disease progression. Cohorts of 3-6 patients receive escalating doses of combretastatin A4 phosphate until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose limiting toxicity. Patients are followed at 3 weeks. PROJECTED ACCRUAL: A maximum of 21 patients will be accrued for this study.

Conditions

Interventions

TypeNameDescription
DRUGfosbretabulin disodium

Timeline

Start date
1998-09-01
Primary completion
2001-07-01
Completion
2001-07-01
First posted
2004-05-03
Last updated
2014-01-07

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00003768. Inclusion in this directory is not an endorsement.