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A Study to Evaluate the Safety and Effectiveness of CNTO 888 Administered Intravenously (IV) in Subjects With Idiopathic Pulmonary Fibrosis (IPF)
This study has been completed.
Study NCT00786201 Information provided by Centocor, Inc.
First Received on November 4, 2008. Last Updated on December 28, 2012
History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Pulmonary Fibrosis
Additional conditions recognized in this trial
Fibrosis
Idiopathic Pulmonary Fibrosis
More general conditions related to this trial
Idiopathic Interstitial Pneumonias
Lung Diseases
Lung Diseases, Interstitial
Pathologic Processes
Respiratory Tract Diseases
Interventions listed in this trial
Placebo
CNTO 888 1 mg/kg
CNTO 888 5 mg/kg
CNTO 888 15 mg/kg
Sponsors listed in this trial
Centocor, Inc.
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