Last updated on May 2020

A Study to Test the Efficacy and Safety of Inhaled TD139 in Subjects With Idiopathic Pulmonary Fibrosis (IPF)


Brief description of study

This is a randomized, double-blind, placebo-controlled phase 2b trial in subjects with IPF (idiopathic pulmonary fibrosis) investigating the efficacy and safety of TD139.

Detailed Study Description

This study is designed to evaluate the efficacy and safety of TD139, a galectin-3 inhibitor, administered by dry powder inhalation over 52 weeks. Subjects will continue on their existing standard of care (SoC), including pirfenidone or nintedanib. Two doses of TD139, each given once per day, will be compared to placebo. A follow up period of up to 52 weeks, where the subjects remain on their designated treatment, will provide valuable information on the longer-term safety of TD139 in IPF.

Clinical Study Identifier: NCT03832946

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SEC Clinical Research

Andalusia, AL United States
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Palmtree Clinical Research Inc

Palm Springs, CA United States
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Paradigm Research

Redding, CA United States
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Broward Research Center

Pembroke Pines, FL United States
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Avanza Medical Research Center

Pensacola, FL United States
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Coastal Pulmonary Critical Care PLC

Saint Petersburg, FL United States
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The Emory Clinic

Atlanta, GA United States
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DC Research Works

Marietta, GA United States
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University of Maryland

Baltimore, MD United States
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The Lung Research Center LLC

Chesterfield, MO United States
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Pulmonlx LLC

Greensboro, NC United States
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University of Cincinnati

Cincinnati, OH United States
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Thomas Jefferson University

Philadelphia, PA United States
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Glenfield Hospital

Leicester, United Kingdom
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Wythenshawe Hospital

Manchester, United Kingdom
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Newcastle Royal Victoria Infirmary

Newcastle Upon Tyne, United Kingdom
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UZ Antwerp

Antwerp, Belgium
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Nottingham City Hospital

Nottingham, United Kingdom
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Recruitment Status: Open


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