Clinical Trials Directory

Trials / Terminated

TerminatedNCT00281021

Second Line Erlotinib (Tarceva) Plus Digoxin in Non-Small Cell Lung Cancer

Phase II Trial of Second Line Erlotinib + Digoxin in Patients With Non-Small Cell Lung Cancer

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
26 (actual)
Sponsor
University of Louisville · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the potential benefit of adding Digoxin to erlotinib (Tarceva) treatment for patients with non-small cell lung cancer.

Detailed description

Non-small cell lung cancer (NSCLC) accounts for 80% of all lung cancer cases. The majority of NSCLC patients have advanced disease at the time of diagnosis, which usually requires treatment beyond standard first-line chemotherapy. Until recently, patients were limited in the number of options available for second-line treatment of NSCLC. In 2004, erlotinib was approved by the FDA for second and third-line treatment of NSCLC. Erlotinib is a cancer chemotherapy medication that slows the growth and spread of cancer cells in the body. Recent research suggests that a medication called Digoxin can sensitize cancer cells to respond better to chemotherapy. Digoxin is normally used to treat certain heart conditions by helping the heart beat more strongly and regularly and is not approved by the FDA for the treatment of NSCLC. Investigators hope that subject response rates to standard erlotinib therapy will be significantly improved by the addition of Digoxin. The purpose of this study is to determine the tumor response rate and overall survival of patients with non-small cell lung cancer treated with a daily regimen of erlotinib (Tarceva) plus Digoxin.

Conditions

Interventions

TypeNameDescription
DRUGErlotinib plus DigoxinEach subject will receive erlotinib and digoxin daily until progression.

Timeline

Start date
2006-02-01
Primary completion
2010-12-01
Completion
2010-12-01
First posted
2006-01-24
Last updated
2018-03-29
Results posted
2014-11-10

Source: ClinicalTrials.gov record NCT00281021. Inclusion in this directory is not an endorsement.