Viewing Study NCT00043342



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Study NCT ID: NCT00043342
Status: COMPLETED
Last Update Posted: 2007-11-01
First Post: 2002-08-07

Brief Title: Study of Interferon Gamma-1b by Injection for the Treatment of Patients With Cystic Fibrosis
Sponsor: InterMune
Organization: InterMune

Study Overview

Official Title: A Phase III Study of Interferon Gamma-1b by Subcutaneous Injection for the Treatment of Patients With Cystic Fibrosis
Status: COMPLETED
Status Verified Date: 2007-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this research study is to evaluate the safety tolerability and efficacy of Interferon gamma-1b IFN-gamma 1b when administered by subcutaneous injection over a period of 4 weeks to patients with mild-to-moderate cystic fibrosis Additionally preliminary assessments on the effects of IFN-gamma 1b on lung function and other indicators of health will be made
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None