Kansas City, Kansas 66103

  • Pulmonary Fibrosis

Purpose:

The purpose of this study is to provide an initial evaluation of the effectiveness of BMS-986278 in participants with lung fibrosis, to demonstrate the safety of BMS-986278, and provide information on the drug levels of BMS-986278 in these participants.


Criteria:

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com. Inclusion Criteria: For the idiopathic pulmonary fibrosis (IPF) Cohort - Diagnosis of IPF within 7 years - Female and males ≥ 40 years of age For the progressive fibrotic interstitial lung disease (PF-ILD) Cohort - Evidence of progressive ILD within the 24 months before screening - Female and male ≥ 21 years of age. Exclusion Criteria: - Women of childbearing potential (WOCBP) - Active Smokers - Patients with current malignancy - History of allergy to BMS-986278 or related compounds Other protocol-defined inclusion/exclusion criteria apply


NCT ID:

NCT04308681


Primary Contact:

Study Director
Bristol-Myers Squibb
Bristol-Myers Squibb

Recruiting sites have contact information. Please contact the sites directly. If there is no contact information
Phone: please email:
Email: Clinical.Trials@bms.com


Backup Contact:

First line of the email MUST contain NCT # and Site #.


Location Contact:

Kansas City, Kansas 66103
United States

Mark Hamblin, Site 0031
Phone: 504-905-7812

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: August 03, 2021

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