11 Nov 2015 07:00
VERONA PHARMA PLC - RPL554 paper published in American Journal of PhysiologyVERONA PHARMA PLC - RPL554 paper published in American Journal of Physiology
PR Newswire
London, November 10
Verona Pharma plc
("Verona Pharma" or the "Company")
Paper demonstrating that RPL554 enhances CTFR activation in cystic fibrosis airway epithelia published in American Journal of Physiology
11 November 2015, Cardiff – Verona Pharma plc (AIM: VRP.L), the drug development company focused on first-in-class medicines to treat respiratory diseases, announces that a paper examining the effect of Verona Pharma’s dual PDE3/4 inhibitor, RPL554, on the Cystic Fibrosis Transmembrane conductance Regulator (CFTR), an anion channel that is mutated in cystic fibrosis (CF), has been published. The paper, entitled: “The dual phosphodiesterase 3 and 4 inhibitor RPL554 stimulates CFTR and ciliary beating in primary cultures of bronchial epithelia” was published on-line in the peer reviewed Journal “American Journal of Physiology - Lung Cellular and Molecular Physiology” on 6 November 2015.
In pre-clinical models of CF, RPL554 was shown to have CFTR-stimulatory properties and that CFTR activation by RPL554 is mediated by its inhibition of PDE4 in cells from CF patients with the R117H/F508del mutation. RPL554-induced CFTR activity was further increased by the CFTR potentiator Kalydeco (ivacaftor, VX770) suggesting additional potential benefit by the drug combination.* The work was partly funded through the Venture and Innovation Award which Verona Pharma received from the UK CF Trust in November 2014.
RPL554 is Verona Pharma’s lead pipeline asset. It is a first-in-class drug initially being evaluated in Phase II clinical trials as a nebulised treatment for acute exacerbations of COPD in the hospital setting.
Dr Jan-Anders Karlsson, the CEO of Verona Pharma, said:
“The results of this research further support our view that RPL554 has potential in a number of discrete indications. This peer-reviewed paper suggests that the drug could be a novel therapeutic option for the treatment of patients with cystic fibrosis. The data demonstrate that inhaled RPL554 activates CFTR, and stimulates an increase in ciliary beat frequency, thus having the potential to increase mucociliary clearance and as a consequence the ability to help to reinstate a central function impaired in this disease. We look forward to further exploring the possible use of RPL554 in cystic fibrosis, as well as reporting data from our Phase II trials of RPL554 in COPD and asthma in the first half of 2016.”
The full abstract for this paper is reproduced below.
* This paper extends the research presented at the 2014 and 2015 North American Cystic Fibrosis Conference in the USA, announced in Company press releases on 29 September 2014 and 8 October 2015 respectively.
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Title: The dual phosphodiesterase 3 and 4 inhibitor RPL554 stimulates CFTR and ciliary beating in primary cultures of bronchial epithelia
Mark John Turner, Elizabeth Matthes, Arnaud Billet, Amy J. Ferguson, David Y. Thomas, Scott H Randell, Lawrence E. Ostrowski, Kathy Abbott-Banner, John W. Hanrahan
American Journal of Physiology - Lung Cellular and Molecular Physiology
Published 6 November 2015
DOI: 10.1152/ajplung.00324.2015
Cystic fibrosis (CF), a genetic disease caused by mutations in the CFTR gene, is a life-limiting disease characterized by chronic bacterial airway infection and severe inflammation. Some CFTR mutants have reduced responsiveness to cAMP/PKA signalling, hence pharmacological agents that elevate intracellular cAMP are potentially useful for the treatment of CF. By inhibiting cAMP breakdown, phosphodiesterase (PDE) inhibitors stimulate CFTR in vitro and in vivo. Here, we demonstrate that PDE inhibition by RPL554, a drug which has been shown to cause bronchodilation in asthma and COPD patients, stimulates CFTR-dependent ion secretion across bronchial epithelial cells isolated from patients carrying the R117H/F508del CF genotype. RPL554-induced CFTR activity was further increased by the potentiator VX-770, suggesting additional benefit by the drug combination. RPL554 also increased cilia beat frequency in primary human bronchial epithelial cells. The results indicate RPL554 may increase mucociliary clearance through stimulation of CFTR and increasing ciliary beat frequency and thus could provide a novel therapeutic option for CF.
-Ends-
For further information please contact:
| Verona Pharma plc | Tel: +44 (0)20 3283 4200 |
| Jan-Anders Karlsson, Chief Executive Officer | |
| N+1 Singer | Tel: +44 (0)20 7496 3000 |
| Aubrey Powell / Jen Boorer | |
| FTI Consulting | Tel: +44 (0)20 3727 1000 |
| Simon Conway / Stephanie Cuthbert /Natalie Garland-Collins |
Notes to Editors
About Verona Pharma plc
Verona Pharma plc is a UK-based clinical stage biopharmaceutical company focused on the development of innovative prescription medicines to treat respiratory diseases with significant unmet medical needs, such as chronic obstructive pulmonary disease (COPD), asthma and cystic fibrosis.
Verona Pharma's lead drug, RPL554, is a first-in-class drug currently in Phase II trials as a nebulised treatment for acute exacerbations of COPD in the hospital setting. The drug is a dual phosphodiesterase (PDE) 3/4 inhibitor and therefore has both bronchodilator and anti-inflammatory effects, which are essential to the improvement of patients with COPD and asthma.
Verona Pharma is also building a broader portfolio of RPL554-containing products to maximise its benefit to patients and its value. This includes the very significant markets for COPD and asthma maintenance therapy. The Company is also exploring the potential of the drug in different diseases, such as cystic fibrosis, where it is in pre-clinical testing and has received a Venture and Innovation Award from the Cystic Fibrosis Trust.