Arbutus Biopharma Corporation (Nasdaq: ABUS) (“Arbutus” or the
“Company”), a clinical-stage biopharmaceutical company leveraging
its extensive virology expertise to develop novel therapeutics that
target specific viral diseases, today announced the appointment of
Dr. Karen Sims as Chief Medical Officer and Mr. Christopher
Naftzger as General Counsel and Chief Compliance Officer. Mr.
Naftzger succeeds Dr. Elizabeth Howard who will continue in an
advisory role with respect to the on-going patent infringement
litigations. Both Dr. Sims and Mr. Naftzger will report directly to
William Collier, Arbutus President and Chief Executive Officer,
effective immediately.
“We are excited to welcome Karen and Chris to
the executive management team,” commented Mr. Collier. “Karen has
played an integral role in the clinical development of AB-729, our
lead RNAi therapeutic, during her six-year tenure at Arbutus, and
has continued to advance our pipeline of HBV programs. I am
confident that under her leadership, the clinical team will
continue to effectively execute our mission to develop curative
regimens for patients with chronic HBV.”
Mr. Collier continued, “Chris brings over a
decade of experience serving as in-house general counsel for life
science companies, making him well equipped to assist the company
in its next stage of development. We expect this to be a seamless
transition for the legal department as Liz continues to support the
Company, serving in an advisory role with respect to our ongoing
patent infringement litigation cases. On behalf of the entire
Arbutus team and Board of Directors, I would like to thank Liz for
her contributions over the last seven years as part of our legal
team in addition to her many prior years of service as our external
counsel. Liz has been instrumental in overseeing all legal
initiatives for the Company and I’m thankful we will continue to
benefit from her expertise moving forward as she serves in an
advisory role.”
Dr. Karen Sims, MD, PhD, joined Arbutus in April
2017 and has held positions of increasing seniority, including most
recently as Vice President, Clinical Development, before being
promoted to Chief Medical Officer. Dr. Sims is a board-certified
infectious disease physician with more than 12 years of industry
experience in conducting and overseeing early stage through global
Phase 2 clinical trials. Prior to joining Arbutus, Dr. Sims held
multiple positions during her seven-year tenure at Bristol-Myers
Squibb (NYSE: BMY). Most recently she served as Medical Director in
the Virology and Immunoscience therapeutic areas where she oversaw
Phase 1 and 2 trials in the HCV direct-acting antiviral program and
several HIV discovery programs, as well as support for HIV marketed
products. Previously, Karen was an Attending Physician and
Instructor in Medicine at the Hospital of the University of
Pennsylvania, with a focus on solid organ transplant infectious
disease, HIV clinical care and translational research in lung
transplantation. Dr. Sims obtained her BS in Biological
Psychology at Bates College, her PhD in Neuroscience from the
University of Pennsylvania, and received her MD from the University
of Pennsylvania School of Medicine. Karen completed her Internal
Medicine and Infectious Diseases training at the Hospital of the
University of Pennsylvania.
Christopher Naftzger joins Arbutus with more
than 25 years of legal experience, including over a decade of
experience serving as senior in-house counsel with life science
companies. Most recently he served as Interim-CEO, General Counsel
and Corporate Secretary of Nabriva Therapeutics (Nasdaq: NBRV), a
commercial-stage antibiotic company, where over the course of five
years he held various roles including Vice President, Deputy
General Counsel and Assistant Secretary. Mr. Naftzger has also
served as General Counsel and Corporate Secretary of Krystal
Biotech (Nasdaq: KRYS), an emerging-stage, gene therapy company and
Vice President, General Counsel, Chief Compliance Officer, and
Secretary of Unilife Medical Solutions, a developer and
manufacturer of innovative drug delivery systems. He has held
senior in-house counsel positions with Chesapeake Corporation and
Koch Industries and was a corporate partner with Blank Rome LLP in
Washington, DC. Mr. Naftzger obtained his undergraduate degree from
Hampden-Sydney College and his law degree from the Willamette
University College of Law.
Inducement Grants under Nasdaq Listing
Rule 5635(c)(4)
In connection with the hiring of Mr. Naftzger,
the Compensation Committee of the Arbutus Board of Directors
granted to Mr. Naftzger an option to purchase an aggregate of
500,000 common shares as an inducement award material to Mr.
Naftzger’s entering into employment with the Company in accordance
with Nasdaq Listing Rule 5635(c)(4). The option has an exercise
price equal to the closing price of Arbutus’ common stock on July
10, 2023 and will vest over a four-year period with 25% vesting on
the first anniversary and the remaining 75% vesting in
substantially equal increments monthly over the next three-year
period thereafter, subject to the terms of the grant. The option
was granted outside of the Company’s 2016 Omnibus Share and
Incentive Plan, as supplemented and amended.
About HBV
Hepatitis B is a potentially life-threatening
liver infection caused by the hepatitis B virus (HBV). HBV can
cause chronic infection which leads to a higher risk of death from
cirrhosis and liver cancer. Chronic HBV infection represents a
significant unmet medical need. The World Health Organization
estimates that over 290 million people worldwide suffer from
chronic HBV infection, while other estimates indicate that
approximately 2.4 million people in the United States suffer from
chronic HBV infection. Approximately 820,000 people die every year
from complications related to chronic HBV infection despite the
availability of effective vaccines and current treatment
options.
About Arbutus
Arbutus Biopharma Corporation (Nasdaq: ABUS) is
a clinical-stage biopharmaceutical company leveraging its extensive
virology expertise to develop novel therapeutics that target
specific viral diseases. Our current focus areas include Hepatitis
B virus (HBV), SARS-CoV-2, and other coronaviruses. To address HBV,
we are developing a RNAi therapeutic, an oral PD-L1 inhibitor, and
an oral RNA destabilizer to potentially identify a combination
regimen with the aim of providing a functional cure for patients
with chronic HBV by suppressing viral replication, reducing surface
antigen and reawakening the immune system. We believe our lead
compound, AB-729, is the only RNAi therapeutic with evidence of
immune re-awakening. AB-729 is currently being evaluated in
multiple phase 2 clinical trials. We also have an ongoing drug
discovery and development program directed to identifying novel,
orally active agents for treating coronaviruses, (including
SARS-CoV-2), for which we have nominated a compound and have begun
IND-enabling pre-clinical studies. In addition, we are also
exploring oncology applications for our internal PD-L1 portfolio.
For more information, visit www.arbutusbio.com.
Forward-Looking Statements and
Information
This press release contains forward-looking
statements within the meaning of the Section 27A of the Securities
Act of 1933 and Section 21E of the Securities Exchange Act of 1934,
and forward-looking information within the meaning of Canadian
securities laws (collectively, forward-looking statements).
Forward-looking statements in this press release include statements
about our future development plans for our product candidates.
With respect to the forward-looking statements
contained in this press release, Arbutus has made numerous
assumptions regarding, among other things: the effectiveness and
timeliness of preclinical studies and clinical trials, and the
usefulness of the data; the timeliness of regulatory approvals; the
continued demand for Arbutus’ assets; and the stability of economic
and market conditions. While Arbutus considers these assumptions to
be reasonable, these assumptions are inherently subject to
significant business, economic, competitive, market and social
uncertainties and contingencies, including uncertainties and
contingencies related to patent litigation matters.
Additionally, there are known and unknown risk
factors which could cause Arbutus’ actual results, performance or
achievements to be materially different from any future results,
performance or achievements expressed or implied by the
forward-looking statements contained herein. Known risk factors
include, among others: anticipated pre-clinical studies and
clinical trials may be more costly or take longer to complete than
anticipated, and may never be initiated or completed, or may not
generate results that warrant future development of the tested
product candidate; Arbutus may elect to change its strategy
regarding its product candidates and clinical development
activities; Arbutus may not receive the necessary regulatory
approvals for the clinical development of Arbutus’ products;
economic and market conditions may worsen; uncertainties associated
with litigation generally and patent litigation specifically;
Arbutus and its collaborators may never realize the expected
benefits of the collaborations; and market shifts may require a
change in strategic focus.
A more complete discussion of the risks and
uncertainties facing Arbutus appears in Arbutus’ Annual Report on
Form 10-K, Arbutus’ Quarterly Reports on Form 10-Q and Arbutus’
continuous and periodic disclosure filings, which are available
at www.sedar.com and at www.sec.gov. All
forward-looking statements herein are qualified in their entirety
by this cautionary statement, and Arbutus disclaims any obligation
to revise or update any such forward-looking statements or to
publicly announce the result of any revisions to any of the
forward-looking statements contained herein to reflect future
results, events or developments, except as required by
law.
Contact Information
Investors and MediaLisa M. CaperelliVice
President, Investor RelationsPhone: 215-206-1822Email:
lcaperelli@arbutusbio.com
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