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Completed Phase 1Phase 2 Interventional

Interferon Gamma-1b by Inhalation for the Treatment of Patients With Cystic Fibrosis

ClinicalTrials.gov ID: NCT00043316

Public ClinicalTrials.gov record NCT00043316. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 11:35 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase I/II Study of Interferon Gamma-1b by Inhalation for the Treatment of Patients With Cystic Fibrosis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this research study is to evaluate the safety and effectiveness of Interferon gamma-1b (IFN-g 1b) on lung function when given to patients with cystic fibrosis by inhalation (breathed into the lungs) three times a week for 12 weeks. The FDA has not approved Interferon gamma-1b for use with cystic fibrosis patients, which is the condition being examined in this study.

Study identification

NCT ID
NCT00043316
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
InterMune
Industry
Enrollment
66 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 2001 (Type not available)
Primary completion
Not listed
Completion
Oct 2002 (Actual)
Last update posted
Nov 1, 2007

2001 – 2002

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Phoenix Arizona — —
Not listed Palo Alto California — —
Not listed Sacramento California — —
Not listed San Diego California — —
Not listed San Francisco California — —
Not listed Denver Colorado — —
Not listed Daytona Beach Florida — —
Not listed Orlando Florida — —
Not listed Chicago Illinois — —
Not listed New Orleans Louisiana — —
Not listed Rochester Minnesota — —
Not listed New York New York — —
Not listed Philadelphia Pennsylvania — —
Not listed Nashville Tennessee — —
Not listed Lackland Air Force Base Texas — —
Not listed Tyler Texas — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00043316, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 1, 2007 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00043316 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →