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Etanercept for Non-Infectious Lung Injury Following Bone Marrow Transplantation

Primary Purpose

Respiratory Distress Syndrome, Adult, Bronchiolitis Obliterans, Pneumonia

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
etanercept
Sponsored by
FDA Office of Orphan Products Development
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Respiratory Distress Syndrome, Adult focused on measuring TNFR-Fc fusion protein, Stem Cell Transplantation, Transplantation, Homologous, Respiratory Function Tests

Eligibility Criteria

12 Months - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • University of Michigan

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
January 10, 2002
Last Updated
March 24, 2015
Sponsor
FDA Office of Orphan Products Development
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1. Study Identification

Unique Protocol Identification Number
NCT00029328
Brief Title
Etanercept for Non-Infectious Lung Injury Following Bone Marrow Transplantation
Official Title
Soluble Tumor Necrosis Factor Receptor: Enbrel (Etanercept) for the Treatment of Acute Pulmonary Dysfunction (Idiopathic Pneumonia Syndrome) Following Allogeneic Stem Cell Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
November 2001
Overall Recruitment Status
Completed
Study Start Date
September 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2003 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
FDA Office of Orphan Products Development

4. Oversight

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Distress Syndrome, Adult, Bronchiolitis Obliterans, Pneumonia
Keywords
TNFR-Fc fusion protein, Stem Cell Transplantation, Transplantation, Homologous, Respiratory Function Tests

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
15 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
etanercept

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Months
Accepts Healthy Volunteers
No
Eligibility 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kenneth Cooke, M.D.
Organizational Affiliation
University of Michigan, Ann Arbor, MI
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

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Etanercept for Non-Infectious Lung Injury Following Bone Marrow Transplantation

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