Meaningful Endpoints for Idiopathic Pulmonary Fibrosis (IPF) Clinical Trials: Emphasis on 'Feels, Functions, Survives'. Report of a Collaborative Discussion in a Symposium with Direct Engagement from Representatives of Patients, Investigators, The...
Overview
Authors
Affiliations
Idiopathic pulmonary fibrosis (IPF) carries significant mortality and unpredictable progression, with limited therapeutic options. Designing trials with patient-meaningful endpoints, enhancing the reliability and interpretability of results, and streamlining the regulatory approval process are of critical importance to advancing clinical care in IPF. A landmark in-person symposium in June 2023 assembled 43 participants from the US and internationally, including patients with IPF, investigators, and regulatory representatives, to discuss the immediate future of IPF clinical trial endpoints. Patient advocates were central to discussions, which evaluated endpoints according to regulatory standards and the FDA's 'feels, functions, survives' criteria. Three themes emerged: ) consensus on endpoints mirroring the lived experiences of patients with IPF; ) consideration of replacing forced vital capacity (FVC) as the primary endpoint, potentially by composite endpoints that include 'feels, functions, survives' measures or FVC as components; ) support for simplified, user-friendly patient-reported outcomes (PROs) as either components of primary composite endpoints or key secondary endpoints, supplemented by functional tests as secondary endpoints and novel biomarkers as supportive measures (FDA Guidance for Industry (Multiple Endpoints in Clinical Trials) available at: https://www.fda.gov/media/162416/download). This report, detailing the proceedings of this pivotal symposium, suggests a potential turning point in designing future IPF clinical trials more attuned to outcomes meaningful to patients, and documents the collective agreement across multidisciplinary stakeholders on the importance of anchoring IPF trial endpoints on real patient experiences-namely, how they feel, function, and survive. There is considerable optimism that clinical care in IPF will progress through trials focused on patient-centric insights, ultimately guiding transformative treatment strategies to enhance patients' quality of life and survival.
Somogyi V, Delameillieure A, Schenk S, Van Bulck L, Breuls S, Uckuyu N Respir Res. 2025; 26(1):81.
PMID: 40022111 PMC: 11871732. DOI: 10.1186/s12931-025-03146-4.
Objective measurement of cough in pulmonary fibrosis: a cohort study - ImpaCT.
Kebbe J, Hart S, Kaner R, Kulkarni T, Wollin L, Coeck C ERJ Open Res. 2024; 10(5).
PMID: 39351380 PMC: 11440380. DOI: 10.1183/23120541.00310-2024.
The Fibrotic Phenotype of Human Precision-Cut Lung Slices Is Maintained after Cryopreservation.
Marimoutou M, Patel V, Kim J, Schaible N, Alvarez J, Hughes J Toxics. 2024; 12(9).
PMID: 39330565 PMC: 11436228. DOI: 10.3390/toxics12090637.
Assessing health-related quality of life in patients with interstitial lung diseases.
Stoltefuss S, Leuschner G, Milger K, Kauke T, Gotschke J, Veit T BMC Pulm Med. 2024; 24(1):452.
PMID: 39272068 PMC: 11401309. DOI: 10.1186/s12890-024-03262-9.
Clinical trial design, end-points, and emerging therapies in pulmonary arterial hypertension.
Weatherald J, Fleming T, Wilkins M, Cascino T, Psotka M, Zamanian R Eur Respir J. 2024; 64(4).
PMID: 39209468 PMC: 11525337. DOI: 10.1183/13993003.01205-2024.