Clinical Trials Directory

Trials / Completed

CompletedNCT00827372

A Study of Vascular Endothelial Growth Factor (VEGF) Inhibition in Patients With Unilateral Upper Extremity Lymphedema Following Treatment for Cancer

A Phase II Study of VEGF Inhibition in Patients With Unilateral Upper Extremity Lymphedema Following Treatment for Cancer

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Kathy Miller · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The major purpose of this study is to determine if a new drug called pazopanib decreases lymphedema in subjects previously treated for cancer. Lymphedema, or swelling of the arm, is a result of damage to the lymphatic vessels in the arm during surgery and/or radiation. The damaged vessels can not adequately drain fluid from the arm, resulting in increased pressure and swelling. Pazopanib has not previously been studied as a treatment for lymphedema.

Detailed description

Pazopanib inhibits the growth of blood vessels in tumors by inhibiting a protein called vascular endothelial growth factor (commonly called VEGF). Pazopanib is not currently approved by the US Food and Drug Administration (FDA) and therefore considered an experimental medication. High levels of VEGF cause blood vessels to leak fluid, increasing the pressure in tumors similar to the increased pressure in lymphedema. Previous studies have found that treatment with pazopanib decreases the fluid pressure in tumors. That is why we think pazopanib might be an effective treatment for lymphedema.

Conditions

Interventions

TypeNameDescription
DRUGPazopanibPazopanib will be administered at a starting dose of 800 mg orally once each day.

Timeline

Start date
2009-01-01
Primary completion
2010-07-01
Completion
2010-07-01
First posted
2009-01-22
Last updated
2023-10-16
Results posted
2014-10-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00827372. Inclusion in this directory is not an endorsement.