作者
Robert P. Frantz,Vallerie V. McLaughlin,Sandeep Sahay,Pilar Escribano Subías,R. Zolty,Raymond L. Benza,Richard N. Channick,Kelly Chin,Anna R. Hemnes,Luke Howard,Olivier Sitbon,Jean‐Luc Vachiéry,Roham T. Zamanian,Matt Cravets,R F Roscigno,David Mottola,Robin Osterhout,Jean‐Marie Bruey,Erin Elman,Cindy‐ann Tompkins,Ed Parsley,Richard Aranda,Lawrence S. Zisman,Hossein A. Ghofrani,Yochai Adir,T. Baillie,David Baratz,Charles Burger,Murali M. Chakinala,Jose Ales Martinez,Marion Delcroix,Nathan Dwyer,Jean M. Elwing,Micah R. Fisher,Verónica Franco,Ekkehard Grünig,Kristin B. Highland,Nicholas S. Hill,Naushad Hirani,Marius M. Hoeper,P Jansa,Anne Keogh,John Kingrey,Manuel López‐Meseguer,John W. McConnell,Sanjay Mehta,Lana Melendres‐Groves,Christian Opitz,Joanna Pepke‐Żaba,Priya Pillutla,Franck Rahaghi,Amresh Raina,Yael Raviv,Jeffrey C. Robinson,John Ryan,Jeffrey S. Sager,Shelley Shapiro,Marc A. Simon,Kerri Smith,I. Sobol,Namita Sood,Leslie Spikes,Stefan Stadler,Wendy B. C. Stevens,Roxana Sulica,R. James White
摘要
Background Morbidity and mortality in pulmonary arterial hypertension (PAH) remain high. Activation of platelet-derived growth factor receptor, colony stimulating factor 1 receptor, and mast or stem cell growth factor receptor kinases stimulates inflammatory, proliferative, and fibrotic pathways driving pulmonary vascular remodelling in PAH. Seralutinib, an inhaled kinase inhibitor, targets these pathways. We aimed to evaluate the efficacy and safety of seralutinib in patients with PAH receiving standard background therapy. Methods The TORREY trial was a phase 2, randomised, multicentre, multinational, double-blind, placebo-controlled study. Patients with PAH from 40 hospital and community sites were randomly assigned 1:1 via interactive response technologies to receive seralutinib (60 mg twice daily for 2 weeks, then increased to 90 mg twice daily as tolerated) or placebo by dry powder inhaler twice daily for 24 weeks. Randomisation was stratified by baseline pulmonary vascular resistance (PVR; <800 dyne·s/cm5 and ≥800 dyne·s/cm5). Patients were eligible if classified as WHO Group 1 PH (PAH), WHO Functional Class II or III, with a PVR of 400 dyne·s/cm5 or more, and a 6 min walk distance of between 150 m and 550 m. The primary endpoint was change in PVR from baseline to 24 weeks. Analyses for efficacy endpoints were conducted in randomly assigned patients (intention-to-treat population). Safety analyses included all patients who received the study drug. TORREY was registered with ClinicalTrials.gov (NCT04456998) and EudraCT (2019-002669-37) and is completed. Findings From Nov 12, 2020, to April 20, 2022, 151 patients were screened for eligibility, and following exclusions, 86 adults receiving PAH background therapy were randomly assigned to seralutinib (n=44; four male, 40 female) or placebo (n=42; four male, 38 female), and comprised the intention-to-treat population. At baseline, treatment groups were balanced except for a higher representation of WHO Functional Class II patients in the seralutinib group. The least squares mean change from baseline to week 24 in PVR was 21·2 dyne·s/cm5 (95% CI −37·4 to 79·8) for the placebo group and −74·9 dyne·s/cm5 (−139·7 to −10·2) for the seralutinib group. The least squares mean difference between the seralutinib and placebo groups for change in PVR was −96·1 dyne·s/cm5 (95% CI −183·5 to −8·8; p=0·03). The most common treatment-emergent adverse event in both treatment groups was cough: 16 (38%) of 42 patients in the placebo group; 19 (43%) of 44 patients in the seralutinib group. Interpretation Treatment with inhaled seralutinib significantly decreased PVR, meeting the primary endpoint of the study among patients receiving background therapy for PAH. Funding Gossamer Bio.