Efficacy and Safety of Bexotegrast for the Treatment of Idiopathic Pulmonary Fibrosis

What is the Purpose of this Study?

This study focuses on individuals who have been diagnosed with idiopathic pulmonary fibrosis (IPF), a condition in which the tiny air sacs in the lungs become damaged. IPF is caused by scarring and the build-up of scar tissue (called fibrosis) in the air sacs. The purpose of the study is to determine the effectiveness and safety of an investigational drug called bexotegrast (PLN-74809) compared to a placebo (inactive substance) for the treatment of IPF. Participants will be randomly assigned to receive either bexotegrast 160 mg, bexotegrast 320 mg, or placebo; they will have a 2 out of 3 (66% chance) of receiving bexotegrast and 1 out of 3 (33% chance) of receiving placebo.


Eligibility

Not Available


Where can I participate?

Beverly


What is the full name of this clinical trial?

A randomized, double-blind, dose-ranging, placebo-controlled study to evaluate the efficacy and safety of PLN-74809 for the treatment of idiopathic pulmonary fibrosis

Study Details
Disease Type/Condition

Other

Principal Investigator

Zaman, Tanzira

Age Group

Adult

Phase

II

IRB Number

STUDY00002995


How do I learn more about this study?
Email
clinicaltrials@cshs.org
Study Detail
Disease Type/Condition

Other

Principal Investigator

Zaman, Tanzira

Age Group

Adult

Phase

II

IRB Number

PLN-74809-IPF-206


Contact
Email
clinicaltrials@cshs.org