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Completed Phase 2 Interventional Results available

Safety Study of Oral Pirfenidone in Patients With Pulmonary Fibrosis/Idiopathic Pulmonary Fibrosis

ClinicalTrials.gov ID: NCT00080223

Public ClinicalTrials.gov record NCT00080223. 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 Jun 26, 2026, 1:53 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

An Open-Label, Phase 2 Study of the Safety of Oral Pirfenidone in Patients With Pulmonary Fibrosis/Idiopathic Pulmonary Fibrosis

Study identification

NCT ID
NCT00080223
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Genentech, Inc.
Industry
Enrollment
83 participants

Conditions and interventions

Interventions

  • Pirfenidone Drug

Drug

Eligibility (public fields only)

Age range
40 Years to 85 Years
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
Aug 30, 2003
Primary completion
Apr 29, 2015
Completion
Apr 29, 2015
Last update posted
Apr 16, 2017

2003 – 2015

United States locations

U.S. sites
27
U.S. states
18
U.S. cities
25
Facility City State ZIP Site status
Not listed Phoenix Arizona 85006
Not listed Pomona California 91767
Not listed San Jose California 95119
Not listed New Haven Connecticut 06520
Not listed Sarasota Florida 34239
Not listed Atlanta Georgia 30322
Not listed Kailua Hawaii 96734
Not listed Lahaina Hawaii 96761
Not listed Nampa Idaho 83686
Not listed Elk Grove Village Illinois 60007
Not listed Boston Massachusetts 02118
Not listed West Roxbury Massachusetts 02132
Not listed St Louis Missouri 63110
Not listed Huntington Station New York 11746
Not listed New York New York 10016
Not listed New York New York 10029-6574
Not listed Rochester New York 14620
Not listed Worthington Ohio 43085
Not listed Portland Oregon 97220
Not listed Portland Oregon 97227
Not listed Lancaster Pennsylvania 17601
Not listed Dallas Texas 75390-8503
Not listed Houston Texas 77005
Not listed San Antonio Texas 78229
Not listed Provo Utah 84604
Not listed Annandale Virginia 22003
Not listed Bremerton Washington 98310 - 3349

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 NCT00080223, 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 Apr 16, 2017 · Synced Jun 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00080223 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →