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| Sponsor: | New York University School of Medicine |
|---|---|
| Information provided by: | New York University School of Medicine |
| ClinicalTrials.gov Identifier: | NCT00212563 |
Purpose
A Safety and Efficacy trial of aerosol Interferon-gamma treatment in Pulmonary Fibrosis
| Condition | Intervention | Phase |
|---|---|---|
|
Idiopathic Pulmonary Fibrosis |
Drug: Aerosol Interferon-gamma treatment |
Phase I Phase II |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
Eligibility| Ages Eligible for Study: | 20 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Abnormal serum laboratory values including:
Contacts and Locations| United States, New York | |
| NYU School of Medicine | |
| New York, New York, United States, 10016 | |
| Principal Investigator: | Rany Condos, MD | NYU School of Medicine |
More Information
| ClinicalTrials.gov Identifier: | NCT00212563 History of Changes |
| Other Study ID Numbers: | 9583-04A |
| Study First Received: | September 13, 2005 |
| Last Updated: | December 20, 2005 |
| Health Authority: | United States: Institutional Review Board |
|
Fibrosis Pulmonary Fibrosis Idiopathic Pulmonary Fibrosis Pathologic Processes Lung Diseases Respiratory Tract Diseases Idiopathic Interstitial Pneumonias Lung Diseases, Interstitial |
Interferon-gamma Interferon-gamma, Recombinant Interferons Antiviral Agents Anti-Infective Agents Therapeutic Uses Pharmacologic Actions Antineoplastic Agents |