Clinical Trials Directory

Trials / Completed

CompletedNCT00309959

ABI-007 in Treating Patients With Persistent or Recurrent Cervical Cancer

A Phase II Evaluation of ABI-007 in the Treatment of Persistent or Recurrent Squamous or Nonsquamous Cell Carcinoma of the Cervix

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
37 (actual)
Sponsor
Gynecologic Oncology Group · Network
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

This phase II trial is studying how well ABI-007 works in treating patients with persistent or recurrent cervical cancer. Drugs used in chemotherapy, such as ABI-007, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing.

Detailed description

OBJECTIVES: I. Estimate the antitumor activity of ABI-007 in patients with persistent or recurrent squamous or nonsquamous cell carcinoma of the cervix who have failed on higher-priority treatment protocols. II. Determine the nature and degree of toxicity of ABI-007 in this cohort of patients. III. To determine the expression of the SPARC (secreted protein, acidic and rich in cysteine) protein in the tumor tissue and plasma (exploratory study) of patients treated with this regimen. OUTLINE: This is an open-label, multicenter study. Patients receive ABI-007 IV over 30 minutes on days 1, 8, and 15. Treatment repeats every 28 days in the absence of disease progression or unacceptable toxicity. Blood samples are collected at baseline and periodically during study for SPARC protein expression analysis by ELISA. Archived tumor tissue samples are also analyzed. After completion of study treatment, patients are followed periodically for up to 5 years.

Conditions

Interventions

TypeNameDescription
DRUGPaclitaxel Albumin-Stabilized Nanoparticle FormulationGiven IV
OTHERLaboratory Biomarker AnalysisCorrelative studies

Timeline

Start date
2006-11-01
Primary completion
2011-02-01
First posted
2006-04-03
Last updated
2019-01-08
Results posted
2019-01-08

Locations

26 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00309959. Inclusion in this directory is not an endorsement.