Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Ann Arbor, Michigan 48109


Purpose:

The purpose of this study is to determine the effects of etanercept, and define the toxicity, when administered to patients with acute non-infectious lung injury (idiopathic pneumonia syndrome, IPS) and with subacute pulmonary dysfunction after allogeneic stem cell transplantation.


Study summary:

Over the last 2 decades, allogeneic bone marrow transplantation (BMT) has emerged as an important treatment option for a number of malignant and non-malignant disorders. Unfortunately, pulmonary dysfunction remains a frequent and severe complication of allogeneic BMT. One of the main chemicals felt to cause lung damage is Tumor Necrosis Factor (TNF). Etanercept is an experimental drug that attempts to block TNF lung damage. Patients will undergo blood tests, x-rays, and a bronchoscopy with broncho-alveolar lavage prior to treatment with etanercept to check for infection. If no infection is evident after 24 hours, the etanercept will be started and administered twice weekly for 4 weeks by subcutaneous injection. There will be weekly blood tests and bronchoscopy after the last drug dose.


Criteria:

Inclusion criteria: - Diagnosis of acute idiopathic pneumonia syndrome (IPS) or sub-acute lung injury - At least 1 year of age for IPS stratum - At least 6 years of age for sub-acute lung injury stratum and able to perform formal pulmonary function testing - At least 14 days since prior treatment with an investigational drug for graft-versus-host disease - Previously treated with allogeneic stem cell or bone marrow transplantation for primary disease Exclusion criteria: - Documented evidence of active systemic or pulmonary infection - Cardiogenic failure as cause of pulmonary dysfunction - Known hypersensitivity to etanercept - Currently receiving dialysis - Currently receiving inotropic medications except dopamine - Pregnant or nursing


NCT ID:

NCT00029328


Primary Contact:

Principal Investigator
Kenneth Cooke, M.D.
University of Michigan, Ann Arbor, MI


Backup Contact:

N/A


Location Contact:

Ann Arbor, Michigan 48109
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 10, 2017

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.