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Bexotegrast in Patients with Idiopathic Pulmonary Fibrosis: The INTEGRIS-IPF Study.
Lancaster, Lisa; Cottin, Vincent; Ramaswamy, Murali; Wuyts, Wim A; Jenkins, R Gisli; Scholand, Mary Beth; Kreuter, Michael; Valenzuela, Claudia; Ryerson, Christopher J; Goldin, Jonathan; Kim, Grace Hyun J; Jurek, Marzena; Decaris, Martin; Clark, Annie; Turner, Scott; Barnes, Chris N; Achneck, Hardean E; Cosgrove, Gregory; Lefebvre, Éric A; Flaherty, Kevin R.
Affiliation
  • Lancaster L; Vanderbilt University Medical Center, Nashville, Tennessee, United States; lisa.lancaster@vumc.org.
  • Cottin V; Louis Pradel University Hospital, Respiratory Medicine, Lyon, France.
  • Ramaswamy M; Pulmonix, LLC and Cone Health, Greensboro, North Carolina, United States.
  • Wuyts WA; K U Leuven, respiratory medicine, Leuven, Belgium.
  • Jenkins RG; Imperial College London, National Heart & Lung Institute, London, United Kingdom of Great Britain and Northern Ireland.
  • Scholand MB; NIHR Nottingham Biomedical Research Centre, Respiratory Research Unit, Nottingham, Nottinghamshire, United Kingdom of Great Britain and Northern Ireland.
  • Kreuter M; University of Nottingham School of Medicine, Division of Respiratory Medicine, Nottingham, United Kingdom of Great Britain and Northern Ireland.
  • Valenzuela C; University of Utah Health, Division of Pulmonary Medicine, Salt Lake City, Utah, United States.
  • Ryerson CJ; University Medical Center of the Johannes Gutenberg University Mainz, Mainz Center for Pulmonary Medicine, Mainz, Rheinland-Pfalz, Germany.
  • Goldin J; Servicio de Neumología, Hospital Universitario de La Princesa, Instituto de Investigación Princesa, Madrid, Spain.
  • Kim GHJ; University of British Columbia, Medicine, Vancouver, British Columbia, Canada.
  • Jurek M; UCLA School Of Medicine, Los Angeles, California, United States.
  • Decaris M; University of California Los Angeles, Department of Radiology, Los Angeles, California, United States.
  • Clark A; MedQIA LLC, Los Angeles, California, United States.
  • Turner S; Former employee of Pliant Therapeutics, Inc, South San Francisco, California, United States.
  • Barnes CN; Pliant Therapeutics, South San Francisco, California, United States.
  • Achneck HE; Pliant Therapeutics, South San Francisco, California, United States.
  • Cosgrove G; Former employee of Pliant Therapeutics, Inc, South San Francisco, California, United States.
  • Lefebvre ÉA; Pliant Therapeutics, South San Francisco, California, United States.
  • Flaherty KR; Former employee of Pliant Therapeutics, Inc, South San Francisco, California, United States.
Article in En | MEDLINE | ID: mdl-38843105
ABSTRACT
RATIONALE Idiopathic pulmonary fibrosis (IPF) is a rare and progressive disease, which causes progressive cough, exertional dyspnea, impaired quality of life and death.

OBJECTIVES:

Bexotegrast (PLN 74809) is an oral, once-daily, investigational drug in development for the treatment of IPF.

METHODS:

This Phase 2a, multicenter, clinical trial, randomized participants with IPF to receive oral, once daily bexotegrast 40 mg, 80 mg, 160 mg, 320 mg, or placebo, with or without background IPF therapy (pirfenidone or nintedanib), in an approximately 31 ratio in each bexotegrast dose cohort, for at least 12 weeks. The primary endpoint was incidence of treatment-emergent adverse events (TEAEs). Exploratory efficacy endpoints included change from baseline in forced vital capacity (FVC); quantitative lung fibrosis (QLF) extent (%) and changes from baseline in fibrosis-related biomarkers. MEASUREMENTS AND MAIN

RESULTS:

Bexotegrast was well tolerated with similar rates of TEAEs in the pooled bexotegrast and placebo groups (62/89 [69.7%] and 21/31 [67.7%], respectively). Diarrhea was the most common TEAE; most participants with diarrhea also received nintedanib. Bexotegrast treated participants experienced a reduction in FVC decline over 12 weeks vs. placebo, with or without background therapy. A dose-dependent antifibrotic effect of bexotegrast was observed with QLF imaging and a decrease in fibrosis-associated biomarkers was observed with bexotegrast vs. placebo.

CONCLUSIONS:

Bexotegrast demonstrated a favorable safety and tolerability profile, up to 12 weeks for the doses studied. Exploratory analyses suggest an antifibrotic effect according to FVC, QLF imaging, and circulating levels of fibrosis biomarkers. Clinical trial registration available at www. CLINICALTRIALS gov, ID NCT04396756. This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives License 4.0 (http//creativecommons.org/licenses/by-nc-nd/4.0/).
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Am J Respir Crit Care Med Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Am J Respir Crit Care Med Year: 2024 Document type: Article