Christian Friedrich
The P2X3 receptor antagonist filapixant in patients with refractory chronic cough: a randomized controlled trial
Friedrich, Christian; Francke, Klaus; Birring, Surinder S.; van den Berg, Jan Willem K.; Marsden, Paul A.; McGarvey, Lorcan; Turner, Alice M.; Wielders, Pascal; Gashaw, Isabella; Klein, Stefan; Morice, Alyn H.
Authors
Klaus Francke
Surinder S. Birring
Jan Willem K. van den Berg
Paul A. Marsden
Lorcan McGarvey
Alice M. Turner
Pascal Wielders
Isabella Gashaw
Stefan Klein
Professor Alyn Morice A.H.Morice@hull.ac.uk
Foundation Chair and Professor of Respiratory Medicine
Abstract
BACKGROUND: P2X3 receptor antagonists seem to have a promising potential for treating patients with refractory chronic cough. In this double-blind, randomized, placebo-controlled study, we investigated the efficacy, safety, and tolerability of the novel selective P2X3 receptor antagonist filapixant (BAY1902607) in patients with refractory chronic cough. METHODS: Following a crossover design, 23 patients with refractory chronic cough (age: 60.4 ± 9.1 years) received ascending doses of filapixant in one period (20, 80, 150, and 250 mg, twice daily, 4-days-on/3-days-off) and placebo in the other. The primary efficacy endpoint was the 24-h cough frequency on Day 4 of each dosing step. Further, subjective cough severity and health-related quality of life were assessed. RESULTS: Filapixant at doses ≥ 80 mg significantly reduced cough frequency and severity and improved cough health-related quality of life. Reductions in 24-h cough frequency over placebo ranged from 17% (80 mg dose) to 37% (250 mg dose), reductions over baseline from 23% (80 mg) to 41% (250 mg) (placebo: 6%). Reductions in cough severity ratings on a 100-mm visual analog scale ranged from 8 mm (80 mg) to 21 mm (250 mg). No serious or severe adverse events or adverse events leading to discontinuation of treatment were reported. Taste-related adverse events occurred in 4%, 13%, 43%, and 57% of patients treated with filapixant 20, 80, 150, and 250 mg, respectively, and in 12% treated with placebo. CONCLUSIONS: Filapixant proved to be efficacious, safe, and-apart from the occurrence of taste disturbances, especially at higher dosages-well tolerated during the short therapeutic intervention. Clinical trial registration EudraCT, eudract.ema.europa.eu, 2018-000129-29; ClinicalTrials.gov, NCT03535168.
Citation
Friedrich, C., Francke, K., Birring, S. S., van den Berg, J. W. K., Marsden, P. A., McGarvey, L., …Morice, A. H. (2023). The P2X3 receptor antagonist filapixant in patients with refractory chronic cough: a randomized controlled trial. Respiratory Research, 24(1), Article 109. https://doi.org/10.1186/s12931-023-02384-8
Journal Article Type | Article |
---|---|
Acceptance Date | Mar 7, 2023 |
Online Publication Date | Apr 11, 2023 |
Publication Date | Apr 11, 2023 |
Deposit Date | Apr 23, 2023 |
Publicly Available Date | Apr 24, 2023 |
Journal | Respiratory research |
Print ISSN | 1465-9921 |
Electronic ISSN | 1465-993X |
Publisher | BioMed Central |
Peer Reviewed | Peer Reviewed |
Volume | 24 |
Issue | 1 |
Article Number | 109 |
DOI | https://doi.org/10.1186/s12931-023-02384-8 |
Keywords | Cough reflex sensitivity; Airway hyperreactivity; Airway hyperresponsiveness; Receptor pharmacology; P2X3 receptor antagonist; Refractory chronic cough; Taste disturbances; Proof of concept |
Public URL | https://hull-repository.worktribe.com/output/4267535 |
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© The Author(s) 2023.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
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