NCT06097260

Randomized, Double-blind Study of Efficacy and Safety of Bexotegrast (PLN-74809) for Idiopathic Pulmonary Fibrosis

A Randomized, Double-blind, Dose-ranging, Placebo-controlled Study to Evaluate the Efficacy and Safety of Bexotegrast (PLN-74809) for the Treatment of Idiopathic Pulmonary Fibrosis (BEACON-IPF)
Pliant Therapeutics, Inc.·Phase 2·ClinicalTrials.gov·drugRecruiting
View on ClinicalTrials.gov
Study focus
Drug/Device/Intervention
PLN-74809
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Pliant Therapeutics, Inc.
Location
Redding,Leesburg,Indianapolis,Omaha,Greensboro,Winston-Salem,Bend,DuBois,Pittsburgh,North Charleston,Franklin,El Paso,McKinney,McKinney,Salt Lake City,Midland, Australia,United States of America
Timeline & enrollment
Phase
Phase 2
Start date
Oct 15, 2023
End date
Sep 30, 2025
Enrollment
267 participants
Primary outcome

Change from baseline in absolute FVC (mL)

Summary

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

ICD-10 classifications
Other interstitial pulmonary diseases with fibrosisCystic fibrosis with pulmonary manifestationsCystic fibrosisGraphite fibrosis (of lung)Pulmonary heart disease, unspecified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06097260
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06097260 through Pure Global AI's free database. This Phase 2 trial is sponsored by Pliant Therapeutics, Inc. and is currently Recruiting. The study focuses on Idiopathic Pulmonary Fibrosis. Target enrollment is 267 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.