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Terminated Phase 2 Interventional

A Study to Characterize the Safety, PK and Biological Activity of CC-930 in Idiopathic Pulmonary Fibrosis (IPF)

ClinicalTrials.gov ID: NCT01203943

Public ClinicalTrials.gov record NCT01203943. 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 30, 2026, 11:20 PM 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 Sequential, Ascending Dose Study to Characterize the Safety, Tolerability, Pharmacokinetic and Biological Activity of CC-930 in Idiopathic Pulmonary Fibrosis (IPF)

Brief summary

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

The primary purpose of the study is to evaluate the safety and PK profile of CC-930 in idiopathic pulmonary fibrosis patients.

Study identification

NCT ID
NCT01203943
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Celgene
Industry
Enrollment
28 participants

Conditions and interventions

Eligibility (public fields only)

Age range
50 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
Jan 1, 2011 (Actual)
Primary completion
Jan 31, 2012 (Actual)
Completion
Aug 24, 2012 (Actual)
Last update posted
Nov 19, 2019

2011 – 2012

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294 —
UC Davis Medical Center, Division of Pulmonary and Critical Care Medicine Sacramento California 95817 —
Stanford University, Pulmonary & Critical Care Clinic Stanford California 94305 —
University of Miami Miller School of Medicine Miami Florida 33101 —
University of Louisville Louisville Kentucky 40202 —
University of Minnesota Minneapolis Minnesota 55455 —
Mayo Clinic Rochester Minnesota 55905 —
Mount Sinai Medical Center New York New York 10029 —
Duke University Medical Center Durham North Carolina 27705 —
University of Cincinnati Cincinnati Ohio 45267 —
Geisenger Center for Clinical Studies Danville Pennsylvania 17822 —
Medical University of South Carolina Charleston South Carolina 29425 —
University of Texas Galveston Texas 77555 —
Baylor College of Medicine Houston Texas 77030 —
University of Utah Salt Lake City Utah 84132 —
Vermont Lung Center Colchester Vermont 05446 —

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 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01203943, 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 19, 2019 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01203943 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →