Verona Pharma plc (AIM: VRP) (Nasdaq: VRNA) (“Verona Pharma”), a
clinical-stage biopharmaceutical company focused on respiratory
diseases, announces that David Zaccardelli, Pharm. D., has been
appointed President and Chief Executive Officer (CEO) with effect
from February 1, 2020. Dr. Zaccardelli has also joined the board of
Verona Pharma. Dr. Zaccardelli brings substantial specialty
pharmaceutical leadership and operational expertise, including most
notably, serving as President and CEO of Dova Pharmaceuticals, Inc.
until its acquisition by Swedish Orphan Biovitrum AB (Sobi) in
November 2019. Previously, Dr. Zaccardelli held several
senior management roles including Chief Operating Officer (COO) at
United Therapeutics Corporation. Jan-Anders Karlsson, Ph.D., Verona
Pharma’s previous CEO, is retiring following 8 years of dedicated
service to the Company to pursue non-executive roles and he has
agreed to provide support to ensure an effective transition.
In addition, Mark W. Hahn, a seasoned
pharmaceutical finance executive, will join Verona Pharma as Chief
Financial Officer (CFO), a non-board position, with effect from
March 1, 2020. Mr. Hahn previously served as the CFO of Dova
Pharmaceuticals, Inc. and Cempra, Inc. and raised over $600 million
to support product development and commercialization activities of
those companies. Piers Morgan will continue to serve as CFO of
Verona Pharma through February 28, 2020 to provide an efficient
transition and complete required financial reporting.
Both Dr. Zaccardelli and Mr. Hahn will be based
in North Carolina in the US, where the majority of the Company’s
clinical team are located, to lead the development and
commercialization of ensifentrine for respiratory diseases
including chronic obstructive pulmonary disease (“COPD”), asthma
and cystic fibrosis (CF).
“We are very pleased to have both Dr.
Zaccardelli and Mr. Hahn join Verona Pharma. They are highly
experienced leaders with a proven track record of working together
to create significant value for shareholders. We believe we have a
strong team in place to lead Verona Pharma into its next phase of
growth. The team will focus on the US and worldwide opportunities
to help COPD patients in need of additional treatment,” said Dr.
David Ebsworth, Chairman of Verona Pharma. “I thank Dr. Karlsson
for his leadership in building Verona Pharma into a strong company
with a Phase 3 program for ensifentrine expected to begin in 3Q
2020, and also Mr. Morgan for his support through the US IPO
process. Together, Dr. Karlsson and Mr. Morgan successfully raised
significant capital, listed Verona Pharma on Nasdaq and used these
funds to generate data supporting the strong efficacy and safety
profile of ensifentrine in COPD. I am pleased they will continue to
support the transition to ensure the further success of Verona
Pharma.”
Dr. Zaccardelli, President and CEO, commented:
“I strongly believe it is a transformational time to join Verona
Pharma to ensure the full potential of ensifentrine, a
first-in-class, inhaled, dual inhibitor of the phosphodiesterase 3
(PDE3) and phosphodiesterase 4 (PDE4) enzymes for the treatment of
respiratory diseases including COPD, asthma and CF. In addition,
the recently reported Phase 2 clinical trial results of
ensifentrine added to inhaled tiotropium, a long acting
anti-muscarinic (“LAMA”) commonly used to treat patients with COPD,
underscores its potential for a significant impact on the treatment
for patients with COPD. Verona Pharma will continue to focus on
developing new treatments for patients with unmet medical
need.”
Dr. Zaccardelli continued, “I am also excited
Mark Hahn is joining Verona as CFO as part of the executive
leadership team. He has extensive experience in both finance and
public pharmaceutical companies having raised more than $600
million to support novel product development at previous companies.
In addition, we have effectively collaborated together in the
leadership of previous companies including Dova resulting in the
acquisition by Sobi.”
Previously, Dr. Zaccardelli served as President
and CEO of Dova Pharmaceuticals from December 2018 until its
acquisition by Sobi in November 2019. Dr. Zaccardelli was the
Acting CEO of Cempra, Inc. from December 2016 until the company’s
merger with Melinta Therapeutics, Inc. in November 2017. From 2004
until 2016, Dr. Zaccardelli served in several senior management
roles at United Therapeutics Corporation, including COO, Chief
Manufacturing Officer and Executive Vice President, Pharmaceutical
Development and Operations. Prior to joining United Therapeutics,
Dr. Zaccardelli founded and led a start-up company focused on
contract pharmaceutical development services, from 1997 through
2003. From 1988 to 1996, Dr. Zaccardelli worked at Burroughs
Wellcome & Co. and Glaxo Wellcome, Inc. in a variety of
clinical research positions. He also served as Director of Clinical
and Scientific Affairs for Bausch & Lomb Pharmaceuticals from
1996 to 1997.
Prior to Verona Pharma, Mr. Hahn served as CFO
of Dova Pharmaceuticals from January 2018 until the acquisition by
Sobi in November 2019 where he led over $100 million in equity and
debt financings and was instrumental in the launch of Dova’s first
commercial product. Mr. Hahn previously served as the CFO of
Cempra, Inc. from 2010 until it was acquired by Melinta
Therapeutics, Inc. in November 2017. While at Cempra, Mr. Hahn
spearheaded all financing activities including the company’s IPO
and follow on offerings raising over $500 million over a seven-year
period. Prior to joining Cempra, from 2008 to 2009, Mr. Hahn
was the CFO for Athenix, a rapidly growing agricultural biotech
company that merged with Bayer CropScience in 2010. Before taking
on operating roles at corporations, Mr. Hahn spent twelve years at
Ernst and Young where he assisted in the IPO process for many
software, manufacturing, and consumer product companies. Mr. Hahn
received a Bachelor of Business Administration degree in Accounting
and Finance from the University of Wisconsin-Milwaukee and is a
Certified Public Accountant.
Additional disclosures required under the AIM
Rules for Companies are included below.
THIS ANNOUNCEMENT CONTAINS INSIDE INFORMATION
FOR THE PURPOSES OF ARTICLE 7 OF REGULATION (EU) NO 596/2014.
About Verona
PharmaVerona Pharma is a clinical-stage biopharmaceutical
company focused on developing and commercializing innovative
therapies for the treatment of respiratory diseases with
significant unmet medical needs. If successfully developed and
approved, Verona Pharma’s product candidate, ensifentrine, has the
potential to be the first therapy for the treatment of respiratory
diseases that combines bronchodilator and anti-inflammatory
activities in one compound. Verona Pharma is currently in Phase 2
development with three formulations of ensifentrine for the
treatment of COPD: nebulized, dry powder inhaler, and pressurized
metered-dose inhaler. Ensifentrine also has potential applications
in cystic fibrosis, asthma and other respiratory diseases. For more
information, please visit www.veronapharma.com.
Forward-Looking StatementsThis
press release contains forward-looking statements. All statements
contained in this press release that do not relate to matters of
historical fact should be considered forward-looking statements,
including, but not limited to, the successful transition of Verona
Pharma’s CEO and CFO roles, the development of ensifentrine, the
progress and timing of clinical trials, data and Phase 3 readiness
of ensifentrine, the potential for ensifentrine to be a
first-in-class phosphodiesterase 3 and 4 inhibitor, and to be the
first therapy for the treatment of respiratory diseases to combine
bronchodilator and anti-inflammatory activities in one compound,
the potential for ensifentrine to have a significant impact on the
treatment of COPD, the potential application of ensifentrine for
the treatment of cystic fibrosis, asthma and other respiratory
diseases, and Verona Pharma continuing its focus on developing new
treatments for patients with unmet medical need.
These forward-looking statements are based on
management's current expectations. These statements are neither
promises nor guarantees, but involve known and unknown risks,
uncertainties and other important factors that may cause our actual
results, performance or achievements to be materially different
from our expectations expressed or implied by the forward-looking
statements, including, but not limited to, the following: our
limited operating history; our need for additional funding to
complete development and commercialization of ensifentrine, which
may not be available and which may force us to delay, reduce or
eliminate our development or commercialization efforts; the
reliance of our business on the success of ensifentrine, our only
product candidate under development; economic, political,
regulatory and other risks involved with international operations;
the lengthy and expensive process of clinical drug development,
which has an uncertain outcome; serious adverse, undesirable or
unacceptable side effects associated with ensifentrine, which could
adversely affect our ability to develop or commercialize
ensifentrine; potential delays in enrolling patients, which could
adversely affect our research and development efforts and the
completion of our clinical trials; we may not be successful in
developing ensifentrine for multiple indications; our ability to
obtain approval for and commercialize ensifentrine in multiple
major pharmaceutical markets; misconduct or other improper
activities by our employees, consultants, principal investigators,
and third-party service providers; our future growth and ability to
compete depends on retaining our key personnel and recruiting
additional qualified personnel; material differences between our
“top-line” data and final data; our reliance on third parties,
including clinical investigators, manufacturers and suppliers, and
the risks related to these parties’ ability to successfully develop
and commercialize ensifentrine; and lawsuits related to patents
covering ensifentrine and the potential for our patents to be found
invalid or unenforceable. These and other important factors under
the caption “Risk Factors” in our Annual Report on Form 20-F filed
with the Securities and Exchange Commission (“SEC”) on March 19,
2019, and our other reports filed with the SEC, could cause actual
results to differ materially from those indicated by the
forward-looking statements made in this press release. Any such
forward-looking statements represent management's estimates as of
the date of this press release. While we may elect to update such
forward-looking statements at some point in the future, we disclaim
any obligation to do so, even if subsequent events cause our views
to change. These forward-looking statements should not be relied
upon as representing our views as of any date subsequent to the
date of this press release.
For further information, please
contact:
Verona Pharma plc |
Tel: +44 (0)20 3283 4200 |
David Zaccardelli, Chief Executive Officer |
info@veronapharma.com |
David Moskowitz, VP Capital Markets Strategy & Investor
Relations (Investor enquiries)Victoria Stewart, Director of
Communications (Media Enquiries) |
|
|
|
N+1 Singer (Nominated Adviser and UK Broker) |
Tel: +44 (0)20 3283 4200 |
Aubrey Powell / George Tzimas / Iqra Amin (Corporate Finance) |
|
Tom Salvesen (Corporate Broking) |
|
|
|
Optimum Strategic Communications(European Media
and Investor Enquiries) |
Tel: +44 (0)20 950 9144 verona@optimumcomms.com |
Mary Clark / Eva Haas / Hollie Vile |
|
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Argot Partners(US Investor Enquiries) |
Tel: +1 212-600-1902verona@argotpartners.com |
Stephanie Marks / Kimberly Minarovich / Michael Barron |
|
Additional Disclosures Required under
the AIM Rules for Companies
In accordance with Schedule 2(g) of the AIM
Rules, Dr. Zaccardelli (aged 55) holds or has held the following
directorships and partnerships in the last five years:
Current |
Past |
Melinta Therapeutics Inc |
Cempra Pharmaceuticals Inc |
CoreRx Inc |
Dova Pharmaceuticals Inc |
Evecxia Therapeutics Inc |
|
Bull City Select Investments LLC
(Managing Member) |
|
Additionally, Melinta Therapeutics Inc, where
Dr. Zaccardelli remains a non-executive director, has filed for
Chapter 11 bankruptcy in Delaware.
There are no additional disclosures required
under AIM Rule 17.
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