Verona Pharma PLC Notice of GM
July 01 2016 - 3:00AM
UK Regulatory
TIDMVRP
Verona Pharma plc
("Verona Pharma" or the "Company")
Confirmation of General Meeting Date
1 July 2016, Cardiff - Verona Pharma plc (AIM: VRP), the drug development
company focused on first-in-class medicines to treat respiratory diseases,
confirms that, further to the Notice of Meeting contained within the Circular
posted to Shareholders on 17 June 2016 in relation to the Proposed Placing, the
General Meeting of the Company will be held at 11.00 a.m. on 22 July 2016 at
the offices of Shakespeare Martineau LLP whose address as of 18 July 2016 is
Allianz House, 6th Floor, 60 Gracechurch Street, London, EC3V 0HR.
Capitalised terms in this announcement have the same meaning as in the Circular
being published in conjunction with the proposed placing.
The expected timetable of principal events remains as previously stated,
namely:
Latest time and date for receipt of completed
Forms of Proxy to be valid at the General Meeting 11.00 a.m. on 20 July
2016
General Meeting 11.00 a.m. on 22 July
2016
Announcement of results of General Meeting 22 July 2016
Admission to trading and commencement of dealings 29 July 2016
in the Placing Shares on AIM
Despatch of definitive share certificates for Placing by 16 August 2016
Shares
in certificated form
Despatch of definitive certificates for Warrants by 16 August 2016
Notes:
(1) References to times are to London time (unless otherwise stated).
(2) If any of the above times or dates should change, the revised times
and/or dates will be notified by an announcement to an RIS and otherwise
communicated to Placees.
(3) Certain of the events in the above timetable are conditional upon,
amongst other things, the approval of the Resolutions to be proposed at the
General Meeting.
(4) The Warrants will not be separately admitted to trading on AIM, but
the Warrant Shares which will arise following any valid exercise of Warrants
will be admitted to trading in due course as part of the single class of shares
admitted to trading on AIM.
-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
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 recently received
a Venture and Innovation Award from the Cystic Fibrosis Trust.
About Chronic Obstructive Pulmonary Disease (COPD)
Sixty-five million people worldwide suffer from moderate to severe COPD and the
World Health Organisation (WHO) expects COPD to be the 3rd leading cause of
death globally by 2020. It is the only major chronic disease with increasing
mortality. Currently available drugs are aimed at long-term maintenance
therapy, with the market dominated by large pharma. Despite the wide
availability of these therapies, COPD patients suffer acute periods of
worsening symptoms (exacerbations), which cause, in the US alone, some 1.5
million A&E visits, 726,000 hospitalisations and 120,000 deaths per annum.
Bronchodilating therapy is considered to be the standard of care, and agents
can be administered via handheld devices such as metered dose inhaler (MDI),
dry powder inhaler (DPI) and by nebulisers. The nebulised bronchodilator
market was worth about $1 billion in 2014 in the US.1 RPL554 is being
developed by Verona Pharma as an add-on therapy to the "Standard of Care" with
the objectives of providing rapid and pronounced improvement in lung function,
reduced symptoms and both shortened duration of hospital stays and reduced
re-admission rates 30 days after discharge from hospital. Studies to date on
RPL554 have demonstrated that it has a strongly differentiated 3-way mode of
action, being: (1) bronchodilation (the relaxation of smooth muscle in the
airway); (2) anti-inflammatory effects on cells and (3) ion channel activation
in epithelial cells, with increased mucociliary clearance of the airway.
1 IMS Consulting Group market research 2014
END
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