Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00047645 · ClinicalTrials.gov registry record · Phase 3

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

A Phase 3 study, sponsored by InterMune.

Completed
Registry status
Phase 3
Development phase
330
Enrollment target

NCT00047645 is a Phase 3 study that has completed, run by InterMune. The registered enrollment target is 330 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00047645, a Phase 3 study, has completed, sponsored by InterMune.

COMPLETED
Registry status
Phase 3
Development phase
330 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG Interferon-gamma 1b

Trial Details

FieldValue
Enrollment Target 330 participants
Start Date 2000-04
Est. Completion 2002-12
Phase Phase 3

Sponsor

InterMune

11 total trials

What the Registry Record Tells You About NCT00047645

The ClinicalTrials.gov registry entry for NCT00047645 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 330 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is InterMune, which has 11 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Interferon-gamma 1b is the first listed.

NCT00047645 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00047645 about?

NCT00047645 is a clinical study titled "A Study of the Safety and Efficacy Interferon-Gamma 1b in Patients With Idiopathic Pulmonary Fibrosis (IPF)". 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...

What is the current status of trial NCT00047645?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 330 participants. The study started on 2000-04. Estimated completion is 2002-12.

What interventions are being tested in trial NCT00047645?

The interventions under investigation include: Interferon-gamma 1b (DRUG).

Who is sponsoring clinical trial NCT00047645?

This trial is sponsored by InterMune, which has 11 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.