Literature DB >> 30201408

Randomized, Double-Blind, Placebo-Controlled, Phase 2 Trial of BMS-986020, a Lysophosphatidic Acid Receptor Antagonist for the Treatment of Idiopathic Pulmonary Fibrosis.

Scott M Palmer1, Laurie Snyder2, Jamie L Todd2, Benjamin Soule3, Rose Christian3, Kevin Anstrom4, Yi Luo3, Robert Gagnon3, Glenn Rosen3.   

Abstract

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) causes irreversible loss of lung function. The lysophosphatidic acid receptor 1 (LPA1) pathway is implicated in IPF etiology. Safety and efficacy of BMS-986020, a high-affinity LPA1 antagonist, was assessed vs placebo in a phase 2 study in patients with IPF.
METHODS: IM136003 was a phase 2, parallel-arm, multicenter, randomized, double-blind, placebo-controlled trial. Adults with IPF (FVC, 45%-90%; diffusing capacity for carbon monoxide, 30%-80%) were randomized to receive placebo or 600 mg BMS-986020 (once daily [qd] or bid) for 26 weeks. The primary end point was rate of change in FVC from baseline to week 26.
RESULTS: Of 143 randomized patients, 108 completed the 26-week dosing phase. Thirty-five patients discontinued prematurely. Patient baseline characteristics were similar between treatment groups (placebo: n = 47; 600 mg qd: n = 48; 600 mg bid: n = 48). Patients treated with BMS-986020 bid experienced a significantly slower rate of decline in FVC vs placebo (-0.042 L; 95% CI, -0.106 to -0.022 vs -0.134 L; 95% CI, -0.201 to -0.068, respectively; P = .049). Dose-related elevations in hepatic enzymes were observed in both BMS-986020 treatment groups. The study was terminated early because of three cases of cholecystitis that were determined to be related to BMS-986020 after unblinding.
CONCLUSIONS: BMS-986020 600 mg bid treatment for 26 weeks vs placebo significantly slowed the rate of FVC decline. Both regimens of BMS-986020 were associated with elevations in hepatic enzymes. TRIAL REGISTRY: ClinicalTrials.gov; No.: NCT01766817; URL: www.clinicaltrials.gov.
Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  clinical trial; idiopathic pulmonary fibrosis; lysophosphatidic acid receptor antagonist

Mesh:

Substances:

Year:  2018        PMID: 30201408     DOI: 10.1016/j.chest.2018.08.1058

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  37 in total

Review 1.  Pharmacotherapy and adjunctive treatment for idiopathic pulmonary fibrosis (IPF).

Authors:  Shigeki Saito; Ala Alkhatib; Jay K Kolls; Yasuhiro Kondoh; Joseph A Lasky
Journal:  J Thorac Dis       Date:  2019-09       Impact factor: 2.895

Review 2.  Idiopathic Pulmonary Fibrosis: New and Emerging Treatment Options.

Authors:  Richard J Hewitt; Toby M Maher
Journal:  Drugs Aging       Date:  2019-06       Impact factor: 3.923

3.  Ablation of lysophosphatidic acid receptor 1 attenuates hypertrophic cardiomyopathy in a mouse model.

Authors:  Anna Axelsson Raja; Hiroko Wakimoto; Daniel M DeLaughter; Daniel Reichart; Joshua Gorham; David A Conner; Mingyue Lun; Clemens K Probst; Norihiko Sakai; Rachel S Knipe; Sydney B Montesi; Barry Shea; Leonard P Adam; Leslie A Leinwand; William Wan; Esther Sue Choi; Eric L Lindberg; Giannino Patone; Michela Noseda; Norbert Hübner; Christine E Seidman; Andrew M Tager; J G Seidman; Carolyn Y Ho
Journal:  Proc Natl Acad Sci U S A       Date:  2022-07-05       Impact factor: 12.779

Review 4.  Ongoing Clinical Trials in Aging-Related Tissue Fibrosis and New Findings Related to AhR Pathways.

Authors:  Hang-Xing Yu; Zhe Feng; Wei Lin; Kang Yang; Rui-Qi Liu; Jia-Qi Li; Xin-Yue Liu; Ming Pei; Hong-Tao Yang
Journal:  Aging Dis       Date:  2022-06-01       Impact factor: 9.968

Review 5.  Molecular imaging of fibrosis: recent advances and future directions.

Authors:  Sydney B Montesi; Pauline Désogère; Bryan C Fuchs; Peter Caravan
Journal:  J Clin Invest       Date:  2019-01-02       Impact factor: 14.808

Review 6.  Lysophosphatidic Acid Signalling in Nervous System Development and Function.

Authors:  Eric Birgbauer
Journal:  Neuromolecular Med       Date:  2020-11-05       Impact factor: 3.843

7.  A study design for statistical learning technique to predict radiological progression with an application of idiopathic pulmonary fibrosis using chest CT images.

Authors:  Grace Hyun J Kim; Yu Shi; Wenxi Yu; Weng Kee Wong
Journal:  Contemp Clin Trials       Date:  2021-03-19       Impact factor: 2.226

Review 8.  Development of antifibrotic therapy for stricturing Crohn's disease: lessons from randomized trials in other fibrotic diseases.

Authors:  Si-Nan Lin; Ren Mao; Chenchen Qian; Dominik Bettenworth; Jie Wang; Jiannan Li; David H Bruining; Vipul Jairath; Brian G Feagan; Min-Hu Chen; Florian Rieder
Journal:  Physiol Rev       Date:  2021-09-27       Impact factor: 37.312

9.  Validation and minimum important difference of the UCSD Shortness of Breath Questionnaire in fibrotic interstitial lung disease.

Authors:  Tao Chen; Amy Po Yu Tsai; Seo Am Hur; Alyson W Wong; Mohsen Sadatsafavi; Jolene H Fisher; Kerri A Johannson; Deborah Assayag; Julie Morisset; Shane Shapera; Nasreen Khalil; Charlene D Fell; Helene Manganas; Gerard Cox; Teresa To; Andrea S Gershon; Nathan Hambly; Andrew J Halayko; Pearce G Wilcox; Martin Kolb; Christopher J Ryerson
Journal:  Respir Res       Date:  2021-07-08

Review 10.  LPA and Autotaxin: Potential Drug Targets in Asthma?

Authors:  Steve N Georas
Journal:  Cell Biochem Biophys       Date:  2021-07-31       Impact factor: 2.989

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.