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A study of the safety and efficacy Interferon-gamma 1b in patients with Idiopathic Pulmonary Fibrosis (IPF)



A study of the safety and efficacy Interferon-gamma 1b in patients with Idiopathic Pulmonary Fibrosis (IPF)

For Condition: Idiopathic Pulmonary Fibrosis
Status: Completed
Sponsor(s): InterMune ,
Synopsis: Study GIPF-001 is phase 3 study designed to determine the safety and efficacy of IFN-g 1b administered by subcutaneous injection; compared to placebo in patients with IPF who are unresponsive to steroids. 330 patients have been enrolled and were assigned to either a IFN-g 1b group or a placebo group.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Placebo Control, Single Group Assignment, Safety/Efficacy Study
Minimum Age/Maximum Age: 20 Years/79 Years
Genders: Both
Protocol Entry Criteria: Male or Female, 20-79 years old
Total Enrollment: 330

Location and Contact Information:

University of Washington Medical Center
Seattle,  Washington,  98195
United States
 


Additional Information:
Study ID Numbers:
  GIPF-001; 
Study Start Date: April 2000
Record last reviewed: January 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00047645

Other Idiopathic Pulmonary Fibrosis Studies:
1. An Open-Label Study of the Safety of Interferon gamma-1b in Patients with IPF

2. Pirfenidone for the Treatment of Patients with Pulmonary Fibrosis/Idiopathic Pulmonary Fibrosis (PF/IPF)

3. The INSPIRE Trial: A Study of Interferon gamma-1b for Idiopathic Pulmonary Fibrosis (IPF)

4. Safety and Tolerability Study of FG-3019 in Patients with Idiopathic Pulmonary Fibrosis

5. A Study of the Safety and Clinical Effects of Interferon gamma-1b in Patients with Idiopathic Pulmonary Fibrosis (IPF)

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Other Idiopathic Pulmonary Fibrosis Clinical Trials
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A study of the safety and efficacy Interferon-gamma 1b in patients with Idiopathic Pulmonary Fibrosis (IPF)

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