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NCT00076635 · ClinicalTrials.gov registry record · Phase 3

An Open-Label Study of the Safety of Interferon Gamma-1b in Patients With IPF

A Phase 3 study, sponsored by InterMune.

Terminated
Registry status
Phase 3
Development phase
91
Enrollment target

NCT00076635: Clinical Trial Phase 3 study, sponsored by InterMune.

NCT00076635 is a Phase 3 study that was terminated before completion, run by InterMune. The registered enrollment target is 91 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00076635, a Phase 3 study, was terminated before completion, sponsored by InterMune.

TERMINATED
Registry status
Phase 3
Development phase
91 participants
Enrollment target

Study Summary

Open-label therapy will be administered to up to 220 patients, following completion of either InterMune Protocol GIPF-002 Part B or Protocol GIPF-004, to assess the long-term safety of subcutaneous Interferon gamma-1b. The study duration will be 5 years.

Interventions

  • DRUG Interferon gamma-1b

Trial Details

FieldValue
Enrollment Target 91 participants
Start Date 2003-11
Est. Completion 2007-04
Phase Phase 3
InterMune

11 total trials

Why NCT00076635 stopped before completion

NCT00076635 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 91 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (88% lower).

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

NCT00076635 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00076635 about?

NCT00076635 is a clinical study titled "An Open-Label Study of the Safety of Interferon Gamma-1b in Patients With IPF". Open-label therapy will be administered to up to 220 patients, following completion of either InterMune Protocol GIPF-002 Part B or Protocol GIPF-004, to assess the long-term safety of subcutaneous Interferon gamma-1b. The study duration will be 5 years.

What is the current status of trial NCT00076635?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 91 participants. The study started on 2003-11. Estimated completion is 2007-04.

What interventions are being tested in trial NCT00076635?

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

Who is sponsoring clinical trial NCT00076635?

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

How this trial's enrollment target compares

Where NCT00076635's enrollment target sits among peer trials

91 1724th of 2000 higher than 277 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00076635, the US trial registry maintained by the National Library of Medicine. NCT00076635 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.