Verona Pharma Applies for Approval to Test RPL554 in UK Clinical Trials

By Verona Pharma Plc, PRNE
Sunday, January 30, 2011

LONDON, January 31, 2011 - Verona Pharma plc (AIM:VRP.L) the biotechnology company dedicated to
discovering new drugs for the treatment of chronic respiratory diseases, has
applied to the Medicines and Healthcare Products Regulatory Agency (MHRA),
the Governmental agency in the UK with responsibility for standards of
safety, quality and performance of new drug treatments, to conduct clinical
trials in the UK.

RPL554 is Verona Pharma's lead drug compound which is a long acting
bronchodilator/anti-inflammatory drug belonging to a class of drugs known as
a mixed phosphodiesterase (PDE) 3/4 inhibitor. Verona Pharma is investigating
its use for the treatment of respiratory diseases including asthma, allergic
rhinitis (hay fever) and chronic obstructive pulmonary disease (COPD).

Professor Michael Walker, CEO of Verona Pharma, said: "The MHRA is a
world renowned regulatory body and the UK is a world centre for respiratory
studies and has a wealth of experience and expertise in this area, having
been responsible for the introduction of most of the inhaled drugs used in
the treatment of asthma and COPD. The application to the MHRA is part of
Verona's strategy to access the best expertise available and to pave the way
for ongoing clinical development and commercialisation in key markets.
Approval by the MHRA to conduct UK trials of RPL554 would be an important
endorsement of the drug's potential therapeutic value."

Whilst licensing discussions for RPL554 continue, the Company is
performing further trials to broaden its knowledge of the therapeutic utility
of RPL554 and to progress the RPL554 programme towards commercialisation.
Further clinical trial data will be provided to potential licensees and is
expected to add value to the RPL554 licensing package. The Company is also
pleased to announce that is has received ethics approval from the appropriate
ethical authority in Italy to proceed with its exploratory Phase II trial in
COPD patients at the Tor Vergata hospital in Rome.

Notes to Editors

About Verona Pharma plc

Verona Pharma plc is a life sciences company dedicated to discovering
drugs for the treatment of chronic respiratory diseases, such as asthma,
allergic rhinitis (hay fever) and chronic obstructive pulmonary disease
(COPD). The Company has three potential drug treatments under development
aimed at the respiratory diseases markets: RPL554, Verona's lead product in
Phase II, Cough (anti-tussive) and novel anti-inflammatory polysaccharides
(NAIPs) for the treatment of a wide range of respiratory diseases.

RPL554

RPL554 is Verona Pharma's lead drug compound which is a long acting
bronchodilator/anti-inflammatory drug (belonging to a class of drugs known as
a mixed phosphodiesterase (PDE) 3/4 inhibitor) for the treatment of asthma,
allergic rhinitis (hay fever) and COPD. The Company has completed a Phase
I/IIa clinical trial of the drug which showed clear clinical benefits in
patients with asthma and allergic rhinitis. The Company is carrying out
further studies of the drug to expand the Phase II data and to test the drug
for the treatment of COPD. The Company is also in discussions to licence the
drug for further development and commercialisation.

Verona Pharma plc: Clive Page, Chairman, Michael Walker, CEO: Tel: +44(0)20-7863-3300, Evolution Securities Limited: Bobby Hilliam/Tim Redfern/Esther Lee: Tel: +44(0)20-7071-4300, College Hill: Melanie Toyne Sewell/Gemma Howe: Tel: +44(0)20-7457-2020, verona at thecollegegroup.com

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