ClinicalTrials.Veeva

Menu

A Study of the Safety and Efficacy Interferon-Gamma 1b in Patients With Idiopathic Pulmonary Fibrosis (IPF)

I

InterMune

Status and phase

Completed
Phase 3

Conditions

Idiopathic Pulmonary Fibrosis

Treatments

Drug: Interferon-gamma 1b

Study type

Interventional

Funder types

Industry

Identifiers

NCT00047645
GIPF-001

Details and patient eligibility

About

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.

Enrollment

330 patients

Sex

All

Ages

20 to 79 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Male or Female, 20-79 years old

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Quadruple Blind

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems