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Terminated Phase 2 Interventional Results available

A Study to Evaluate the Efficacy and Safety of CC-90001 in Subjects With Idiopathic Pulmonary Fibrosis

ClinicalTrials.gov ID: NCT03142191

Public ClinicalTrials.gov record NCT03142191. 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 Jul 21, 2026, 7:05 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 2, 24-Week, Randomized, Double-blind, Placebo-controlled, Multicenter Study, With an 80-Week Active Treatment Extension, to Evaluate the Efficacy and Safety of CC-90001 in Subjects With Idiopathic Pulmonary Fibrosis

Study identification

NCT ID
NCT03142191
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Celgene
Industry
Enrollment
138 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 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
Jul 25, 2017
Primary completion
Dec 23, 2021
Completion
Dec 23, 2021
Last update posted
Jun 27, 2023

2017 – 2021

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
Loma Linda Univ Medical Center Loma Linda California 92354
Cedars Sinai Medical Center Rheumatology Los Angeles California 90048
Local Institution - 514 Sacramento California 95817
University of California Davis Health System Sacramento California 95817
Stanford University Pulmonary and Critical Care Clinic Stanford California 94305
University of Florida Gainesville Florida 32610
University of Miami and Sylvester Cancer Center Miami Florida 33136
University of Louisville Louisville Kentucky 40202
The Lung and Research Center, LLC Chesterfield Missouri 63017
Mt. Sinai School of Medicine New York New York 10029
Duke University Health System - Duke Pulmonary Transplant Clinic Durham North Carolina 27710
University of Cincinnati Medical Center Cincinnati Ohio 45267
University Hospitals Cleveland Medical Center Cleveland Ohio 44121
Pulmonary & Sleep Center of Oklahoma Tulsa Oklahoma 74137
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213
Medical University of South Carolina Charleston South Carolina 29425
Vanderbilt University Medical Center Nashville Tennessee 37212
Baylor University Medical Center Dallas Texas 75246
Local Institution - 502 Dallas Texas 75246
University of Utah Health Care Salt Lake City Utah 84132
University of Vermont Burlington Vermont 05405

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 91 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03142191, 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 Jun 27, 2023 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03142191 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →