Verona Pharma announces positive results for RPL554 in mild asthma at higher doses
The objective of the trial was to establish the appropriate dosage for patients with respect to efficacy and safety. The two doses of RPL554 resulted in positive bronchodilation as assessed by the standard measure of FEV1 (Forced Expiratory Volume at 1 sec). The trial was successfully completed and there were no withdrawals due to adverse effects. Of particular note was the absence of gastrointestinal symptoms related to administration of the drug. The highest dose established at which point limited cardiovascular effects were encountered, thereby allowing the Company to set appropriate dosages for future studies. These results provide further support for RPL554 as a novel treatment for patients with respiratory diseases and further strengthen the Company’s data package for discussions with potential licensees.
Professor Michael Walker, CEO of Verona Pharma said: "The trial has run smoothly, with no major adverse events reported. These positive results underline the excellent bronchodilator effects that can be achieved with RPL554 over a range of doses. These findings were achieved with a nebulized formulation of the drug and the Company continues to work with other formulations of RPL554 in more user-friendly inhaler devices. We look forward to updating shareholders on future studies, and on progress in licensing this novel respiratory drug.”
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